
Unraveling the underlying mechanisms of cancer stem cells in therapeutic resistance for optimizing treatment strategies
Yunhan Tan, Siyuan Qin, Zhe Zhang, Yongen Liu, Li Zhou, Bowen Li, Edouard C. Nice, Yuanyuan Zhang, Jing Jing
MEDCOMM - Oncology ›› 2025, Vol. 4 ›› Issue (1) : e70009.
Unraveling the underlying mechanisms of cancer stem cells in therapeutic resistance for optimizing treatment strategies
The success of cancer therapy has been significantly hampered by various mechanisms of therapeutic resistance. Chief among these mechanisms is the presence of clonal heterogeneity within an individual tumor mass. The introduction of the concept of cancer stem cells (CSCs)—a rare and immature subpopulation with tumorigenic potential that contributes to intratumoral heterogeneity—has deepened our understanding of drug resistance. Given the characteristics of CSCs, such as increased drug-efflux activity, enhanced DNA-repair capacity, high metabolic plasticity, adaptability to oxidative stress, and/or upregulated detoxifying aldehyde dehydrogenase (ALDH) enzymes, CSCs have been recognized as a theoretical reservoir for resistant diseases. Implicit in this recognition is the possibility that CSC-targeted therapeutic strategies might offer a breakthrough in overcoming drug resistance in cancer patients. Herein, we summarize the generation of CSCs and our current understanding of the mechanisms underlying CSC-mediated therapeutic resistance. This extended knowledge has progressively been translated into novel anticancer therapeutic strategies and significantly enriched the available options for combination treatments, all of which are anticipated to improve clinical outcomes for patients experiencing CSC-related relapse.
cancer stem cells (CSCs) / combination therapy / CSC-targeted therapy / drug resistance
[1] |
BrayF, Laversanne M, SungH, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024; 74(3):229-263.
CrossRef
Google scholar
|
[2] |
QinS, JiangJ, LuY, et al. Emerging role of tumor cell plasticity in modifying therapeutic response. Signal Transduct Target Ther. 2020; 5(1):228.
CrossRef
Google scholar
|
[3] |
DongreA, Weinberg RA. New insights into the mechanisms of epithelial–mesenchymal transition and implications for cancer. Nat Rev Mol Cell Biol. 2019; 20(2):69-84.
CrossRef
Google scholar
|
[4] |
LohJ-J, MaS. Hallmarks of cancer stemness. Cell Stem Cell. 2024; 31(5):617-639.
CrossRef
Google scholar
|
[5] |
LewisAC, KatsLM. Non-genetic heterogeneity, altered cell fate and differentiation therapy. EMBO Mol Med. 2021; 13(3):e12670.
CrossRef
Google scholar
|
[6] |
AyobAZ, Ramasamy TS. Cancer stem cells as key drivers of tumour progression. J Biomed Sci. 2018; 25(1):20.
CrossRef
Google scholar
|
[7] |
LiuY, WangH. Biomarkers and targeted therapy for cancer stem cells. Trends Pharmacol Sci. 2024; 45(1):56-66.
CrossRef
Google scholar
|
[8] |
LiouG-Y. CD133 as a regulator of cancer metastasis through the cancer stem cells. Int J Biochem Cell Biol. 2019; 106:1-7.
CrossRef
Google scholar
|
[9] |
YangY, LiX, WangT, Guo Q, XiT, ZhengL. Emerging agents that target signaling pathways in cancer stem cells. J Hematol Oncol. 2020; 13(1):60.
CrossRef
Google scholar
|
[10] |
LiuC, QiangJ, DengQ, et al. ALDH1A1 activity in tumor-initiating cells remodels myeloid-derived suppressor cells to promote breast cancer progression. Cancer Res. 2021; 81(23):5919-5934.
CrossRef
Google scholar
|
[11] |
XuJ, LiL, ShiP, CuiH, YangL. The crucial roles of Bmi-1 in cancer: implications in pathogenesis, metastasis, drug resistance, and targeted therapies. Int J Mol Sci. 2022; 23(15):8231.
CrossRef
Google scholar
|
[12] |
ZhuY, HuangS, ChenS, et al. SOX2 promotes chemoresistance, cancer stem cells properties, and epithelial–mesenchymal transition by β-catenin and Beclin1/autophagy signaling in colorectal cancer. Cell Death Dis. 2021; 12(5):449.
CrossRef
Google scholar
|
[13] |
RegadT. Tissue-specific cancer stem cells: reality or a mirage? Trans Med Rep. 2017;1(1).
CrossRef
Google scholar
|
[14] |
RegadT, SayersT, ReesR. Principles of Stem Cell Biology and Cancer: Future Applications and Therapeutics. John Wiley & Sons; 2015.
|
[15] |
DasM, LawS. Role of tumor microenvironment in cancer stem cell chemoresistance and recurrence. Int J Biochem Cell Biol. 2018; 103:115-124.
CrossRef
Google scholar
|
[16] |
Hernández-CamareroP, JiménezG, López-Ruiz E, BarungiS, MarchalJA, Perán M. Revisiting the dynamic cancer stem cell model: importance of tumour edges. Crit Rev Oncol Hematol. 2018; 131:35-45.
CrossRef
Google scholar
|
[17] |
GoldsteinM, KastanMB. The DNA damage response: implications for tumor responses to radiation and chemotherapy. Annu Rev Med. 2015; 66:129-143.
CrossRef
Google scholar
|
[18] |
KlappV, Álvarez-Abril B, LeuzziG, KroemerG, CicciaA, GalluzziL. The DNA damage response and inflammation in cancer. Cancer Discovery. 2023; 13(7):1521-1545.
CrossRef
Google scholar
|
[19] |
GroellyFJ, FawkesM, DaggRA, Blackford AN, TarsounasM. Targeting DNA damage response pathways in cancer. Nat Rev Cancer. 2023; 23(2):78-94.
CrossRef
Google scholar
|
[20] |
ShibueT, Weinberg RA. EMT, CSCs, and drug resistance: the mechanistic link and clinical implications. Nat Rev Clin Oncol. 2017; 14(10):611-629.
CrossRef
Google scholar
|
[21] |
PanY, ZhouS, LiY, Parshad B, LiW, HaagR. Novel dendritic polyglycerol-conjugated, mesoporous silica-based targeting nanocarriers for co-delivery of doxorubicin and tariquidar to overcome multidrug resistance in breast cancer stem cells. J Control Release. 2021; 330:1106-1117.
CrossRef
Google scholar
|
[22] |
XieXP, LaksDR, SunD, et al. Quiescent human glioblastoma cancer stem cells drive tumor initiation, expansion, and recurrence following chemotherapy. Dev Cell. 2022; 57(1):32-46.e8.
CrossRef
Google scholar
|
[23] |
MingH, LiB, JiangJ, et al. Protein degradation: expanding the toolbox to restrain cancer drug resistance. J Hematol Oncol. 2023; 16(1):6.
CrossRef
Google scholar
|
[24] |
ErinN, Grahovac J, BrozovicA, EfferthT. Tumor microenvironment and epithelial mesenchymal transition as targets to overcome tumor multidrug resistance. Drug Resist Updates. 2020; 53:100715.
CrossRef
Google scholar
|
[25] |
Maugeri-SaccàM, Bartucci M, De MariaR. DNA damage repair pathways in cancer stem cells. Mol Cancer Ther. 2012; 11(8):1627-1636.
CrossRef
Google scholar
|
[26] |
JiaoX, Velasco-Velázquez MA, WangM, et al. CCR5 governs DNA damage repair and breast cancer stem cell expansion. Cancer Res. 2018; 78(7):1657-1671.
CrossRef
Google scholar
|
[27] |
EymeKM, Sammarco A, JhaR, et al. Targeting de novo lipid synthesis induces lipotoxicity and impairs DNA damage repair in glioblastoma mouse models. Sci Transl Med. 2023; 15(679):eabq6288.
CrossRef
Google scholar
|
[28] |
YoshidaGJ. Metabolic reprogramming: the emerging concept and associated therapeutic strategies. J Exp Clin Cancer Res. 2015; 34(1):111.
CrossRef
Google scholar
|
[29] |
TuyK, Rickenbacker L, HjelmelandAB. Reactive oxygen species produced by altered tumor metabolism impacts cancer stem cell maintenance. Redox Biol. 2021; 44:101953.
CrossRef
Google scholar
|
[30] |
CostaRGA, SilvaSLR, DiasIRSB, et al. Emerging drugs targeting cellular redox homeostasis to eliminate acute myeloid leukemia stem cells. Redox Biol. 2023; 62:102692.
CrossRef
Google scholar
|
[31] |
MaY, ZhuY, ShangL, et al. LncRNA XIST regulates breast cancer stem cells by activating proinflammatory IL-6/STAT3 signaling. Oncogene. 2023; 42(18):1419-1437.
CrossRef
Google scholar
|
[32] |
GorodetskaI, Offermann A, PüschelJ, et al. ALDH1A1 drives prostate cancer metastases and radioresistance by interplay with AR-and RAR-dependent transcription. Theranostics. 2024; 14(2):714-737.
CrossRef
Google scholar
|
[33] |
HanJ, WonM, KimJH, et al. Cancer stem cell-targeted bio-imaging and chemotherapeutic perspective. Chem Soc Rev. 2020; 49(22):7856-7878.
CrossRef
Google scholar
|
[34] |
MaiY, SuJ, YangC, Xia C, FuL. The strategies to cure cancer patients by eradicating cancer stem-like cells. Mol Cancer. 2023; 22(1):171.
CrossRef
Google scholar
|
[35] |
WongCC, XuJ, BianX, et al. In colorectal cancer cells with mutant KRAS, SLC25A22-mediated glutaminolysis reduces DNA demethylation to increase WNT signaling, stemness, and drug resistance. Gastroenterology. 2020; 159(6):2163-2180.e6.
CrossRef
Google scholar
|
[36] |
BaysoyA, BaiZ, SatijaR, Fan R. The technological landscape and applications of single-cell multi-omics. Nat Rev Mol Cell Biol. 2023; 24(10):695-713.
CrossRef
Google scholar
|
[37] |
TakaoS, DingQ, MatsubaraS. Pancreatic cancer stem cells: regulatory networks in the tumor microenvironment and targeted therapy. J Hepatobiliary Pancreat Sci. 2012; 19(6):614-620.
CrossRef
Google scholar
|
[38] |
BayikD, LathiaJD. Cancer stem cell–immune cell crosstalk in tumour progression. Nat Rev Cancer. 2021; 21(8):526-536.
CrossRef
Google scholar
|
[39] |
ClaraJA, MongeC, YangY, Takebe N. Targeting signalling pathways and the immune microenvironment of cancer stem cells—a clinical update. Nat Rev Clin Oncol. 2020; 17(4):204-232.
CrossRef
Google scholar
|
[40] |
IshimotoT, NaganoO, YaeT, et al. CD44 variant regulates redox status in cancer cells by stabilizing the xCT subunit of system xc(-) and thereby promotes tumor growth. Cancer Cell. 2011; 19(3):387-400.
CrossRef
Google scholar
|
[41] |
HuangT, SongX, XuD, et al. Stem cell programs in cancer initiation, progression, and therapy resistance. Theranostics. 2020; 10(19):8721-8743.
CrossRef
Google scholar
|
[42] |
SellS, Nicolini A, FerrariP, M BiavaP. Cancer: a problem of developmental biology; scientific evidence for reprogramming and differentiation therapy. Curr Drug Targets. 2016; 17(10):1103-1110.
CrossRef
Google scholar
|
[43] |
YangL, ShiP, ZhaoG, et al. Targeting cancer stem cell pathways for cancer therapy. Signal Transduct Target Ther. 2020; 5(1):8.
CrossRef
Google scholar
|
[44] |
GuY, WangY, HeL, et al. Circular RNA circIPO11 drives self-renewal of liver cancer initiating cells via hedgehog signaling. Mol Cancer. 2021; 20:132.
CrossRef
Google scholar
|
[45] |
ChengL-H, HsuC-C, TsaiH-W, et al. ASPM activates hedgehog and Wnt signaling to promote small cell lung cancer stemness and progression. Cancer Res. 2023; 83(6):830-844.
CrossRef
Google scholar
|
[46] |
WangJ, YuH, DongW, et al. N6-methyladenosine–mediated up-regulation of FZD10 regulates liver cancer stem cells’ properties and lenvatinib resistance through WNT/β-catenin and hippo signaling pathways. Gastroenterology. 2023; 164(6):990-1005.
CrossRef
Google scholar
|
[47] |
ZhangW, RuanX, LiY, et al. KDM1A promotes thyroid cancer progression and maintains stemness through the Wnt/β-catenin signaling pathway. Theranostics. 2022; 12(4):1500-1517.
CrossRef
Google scholar
|
[48] |
HeY, JiangX, DuanL, et al. LncRNA PKMYT1AR promotes cancer stem cell maintenance in non-small cell lung cancer via activating Wnt signaling pathway. Mol Cancer. 2021; 20:156.
CrossRef
Google scholar
|
[49] |
JiangN, ZouC, ZhuY, et al. HIF-1α-regulated miR-1275 maintains stem cell-like phenotypes and promotes the progression of LUAD by simultaneously activating Wnt/β-catenin and Notch signaling. Theranostics. 2020; 10(6):2553-2570.
CrossRef
Google scholar
|
[50] |
NedeljkovićM, Damjanović A. Mechanisms of chemotherapy resistance in triple-negative breast cancer—how we can rise to the challenge. Cells. 2019; 8(9):957.
CrossRef
Google scholar
|
[51] |
BlanpainC. Tracing the cellular origin of cancer. Nature Cell Biol. 2013; 15(2):126-134.
CrossRef
Google scholar
|
[52] |
BlanpainC, SimonsBD. Unravelling stem cell dynamics by lineage tracing. Nat Rev Mol Cell Biol. 2013; 14(8):489-502.
CrossRef
Google scholar
|
[53] |
DzierzakE, BigasA. Blood development: hematopoietic stem cell dependence and independence. Cell Stem Cell. 2018; 22(5):639-651.
CrossRef
Google scholar
|
[54] |
HöferT, Rodewald H-R. Differentiation-based model of hematopoietic stem cell functions and lineage pathways. Blood. 2018; 132(11):1106-1113.
CrossRef
Google scholar
|
[55] |
Garcia-MayeaY, MirC, MassonF, Paciucci R, LLeonartME. Insights into new mechanisms and models of cancer stem cell multidrug resistance. Sem Cancer Biol. 2020; 60:166-180.
CrossRef
Google scholar
|
[56] |
BaiX, NiJ, BeretovJ, Graham P, LiY. Cancer stem cell in breast cancer therapeutic resistance. Cancer Treat Rev. 2018; 69:152-163.
CrossRef
Google scholar
|
[57] |
YamanakaS. Pluripotent stem cell-based cell therapy—promise and challenges. Cell Stem Cell. 2020; 27(4):523-531.
CrossRef
Google scholar
|
[58] |
HurwitzSN, JungSK, KurreP. Hematopoietic stem and progenitor cell signaling in the niche. Leukemia. 2020; 34(12):3136-3148.
CrossRef
Google scholar
|
[59] |
NovakJSS, BakshSC, FuchsE. Dietary interventions as regulators of stem cell behavior in homeostasis and disease. Genes Dev. 2021; 35(3-4):199-211.
CrossRef
Google scholar
|
[60] |
ZhuS, ZhaoD, YanL, et al. BMI1 regulates androgen receptor in prostate cancer independently of the polycomb repressive complex 1. Nat Commun. 2018; 9(1):500.
CrossRef
Google scholar
|
[61] |
Rodriguez-RamirezC, Zhang Z, WarnerKA, et al. p53 inhibits Bmi-1-driven self-renewal and defines salivary gland cancer stemness. Clin Cancer Res. 2022; 28(21):4757-4770.
CrossRef
Google scholar
|
[62] |
BansalN, Bartucci M, YusuffS, et al. BMI-1 targeting interferes with patient-derived tumor-initiating cell survival and tumor growth in prostate cancer. Clin Cancer Res. 2016; 22(24):6176-6191.
CrossRef
Google scholar
|
[63] |
SariIN, PhiLTH, JunN, WijayaYT, LeeS, KwonHY. Hedgehog signaling in cancer: a prospective therapeutic target for eradicating cancer stem cells. Cells. 2018; 7(11):208.
CrossRef
Google scholar
|
[64] |
LegniniI, Emmenegger L, ZappuloA, et al. Spatiotemporal, optogenetic control of gene expression in organoids. Nature Methods. 2023; 20(10):1544-1552.
CrossRef
Google scholar
|
[65] |
SivakumarS, QiS, ChengN, et al. TP53 promotes lineage commitment of human embryonic stem cells through ciliogenesis and sonic hedgehog signaling. Cell Rep. 2022; 38(7):110395.
CrossRef
Google scholar
|
[66] |
LiB, MingH, QinS, et al. HSPA8 activates Wnt/β-catenin signaling to facilitate BRAF V600E colorectal cancer progression by CMA-mediated CAV1 degradation. Adv Sci. 2024; 11(3):2306535.
CrossRef
Google scholar
|
[67] |
BhattacharyaR, Banerjee Mustafi S, StreetM, DeyA, Dwivedi SKD. Bmi-1: at the crossroads of physiological and pathological biology. Genes Dis. 2015; 2(3):225-239.
CrossRef
Google scholar
|
[68] |
CodispotiB, Rinaldo N, ChiarellaE, et al. Recombinant TAT-BMI-1 fusion protein induces ex vivo expansion of human umbilical cord blood-derived hematopoietic stem cells. Oncotarget. 2017; 8(27):43782-43798.
CrossRef
Google scholar
|
[69] |
BiehsB, HuJK-H, StrauliNB, et al. BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor. Nature Cell Biol. 2013; 15(7):846-852.
CrossRef
Google scholar
|
[70] |
HerzogAE, WarnerKA, ZhangZ, et al. The IL-6R and Bmi-1 axis controls self-renewal and chemoresistance of head and neck cancer stem cells. Cell Death Dis. 2021; 12(11):988.
CrossRef
Google scholar
|
[71] |
LiangY, YangL, XieJ. The role of the hedgehog pathway in chemoresistance of gastrointestinal cancers. Cells. 2021; 10(8):2030.
CrossRef
Google scholar
|
[72] |
YanR, PengX, YuanX, et al. Suppression of growth and migration by blocking the hedgehog signaling pathway in gastric cancer cells. Cell Oncol. 2013; 36(5):421-435.
CrossRef
Google scholar
|
[73] |
XiaoY, Thoresen DT, WilliamsJS, et al. Neural hedgehog signaling maintains stem cell renewal in the sensory touch dome epithelium. Proc Natl Acad Sci. 2015; 112(23):7195-7200.
CrossRef
Google scholar
|
[74] |
ZhangC, LiC, HeF, CaiY, YangH. Identification of CD44+ CD24+ gastric cancer stem cells. J Cancer Res Clin Oncol. 2011; 137(11):1679-1686.
CrossRef
Google scholar
|
[75] |
ZhangJ, FanJ, ZengX, et al. Hedgehog signaling in gastrointestinal carcinogenesis and the gastrointestinal tumor microenvironment. Acta Pharm Sin B. 2021; 11(3):609-620.
CrossRef
Google scholar
|
[76] |
SalikB, YiH, HassanN, et al. Targeting RSPO3-LGR4 signaling for leukemia stem cell eradication in acute myeloid leukemia. Cancer Cell. 2020; 38(2):263-278.
CrossRef
Google scholar
|
[77] |
TakebeN, HarrisPJ, WarrenRQ, Ivy SP. Targeting cancer stem cells by inhibiting Wnt, Notch, and Hedgehog pathways. Nat Rev Clin Oncol. 2011; 8(2):97-106.
CrossRef
Google scholar
|
[78] |
Takahashi-YanagaF, Kahn M. Targeting Wnt signaling: can we safely eradicate cancer stem cells? Clin Cancer Res. 2010; 16(12):3153-3162.
CrossRef
Google scholar
|
[79] |
KouryJ, ZhongL, HaoJ. Targeting signaling pathways in cancer stem cells for cancer treatment. Stem Cells Int. 2017; 2017(1):2925869.
CrossRef
Google scholar
|
[80] |
PommierSJ, Hernandez A, HanE, et al. Fresh surgical specimens yield breast stem/progenitor cells and reveal their oncogenic abnormalities. Ann Surg Oncol. 2012; 19(2):527-535.
CrossRef
Google scholar
|
[81] |
ShahM, Cardenas R, WangB, et al. HOXC8 regulates self-renewal, differentiation and transformation of breast cancer stem cells. Mol Cancer. 2017;16:38.
CrossRef
Google scholar
|
[82] |
ZhangH-L, WangP, LuM-Z, Zhang S-D, ZhengL. c-Myc maintains the self-renewal and chemoresistance properties of colon cancer stem cells. Oncol Lett. 2019; 17(5):4487-4493.
|
[83] |
SuR, DongL, LiY, et al. Targeting FTO suppresses cancer stem cell maintenance and immune evasion. Cancer Cell. 2020; 38(1):79-96.e11.
CrossRef
Google scholar
|
[84] |
MichelucciA, Di Cristofano C, LamiA, et al. PIK3CA in breast carcinoma: a mutational analysis of sporadic and hereditary cases. Diagn Mol Pathol. 2009; 18(4):200-205.
CrossRef
Google scholar
|
[85] |
SamuelsY, Diaz, Jr., LA, Schmidt-KittlerO, et al. Mutant PIK3CA promotes cell growth and invasion of human cancer cells. Cancer Cell. 2005; 7(6):561-573.
CrossRef
Google scholar
|
[86] |
KawamotoA, YokoeT, TanakaK, et al. Radiation induces epithelial-mesenchymal transition in colorectal cancer cells. Oncol Rep. 2012; 27(1):51-57.
|
[87] |
MuellerAC, PiperM, GoodspeedA, et al. Induction of ADAM10 by radiation therapy drives fibrosis, resistance, and epithelial-to-mesenchyal transition in pancreatic cancer. Cancer Res. 2021; 81(12):3255-3269.
CrossRef
Google scholar
|
[88] |
ZhangN, NgAS, CaiS, LiQ, YangL, Kerr D. Novel therapeutic strategies: targeting epithelial–mesenchymal transition in colorectal cancer. Lancet Oncol. 2021; 22(8):e358-e368.
CrossRef
Google scholar
|
[89] |
YangJ, AntinP, BerxG, et al. Guidelines and definitions for research on epithelial–mesenchymal transition. Nat Rev Mol Cell Biol. 2020; 21(6):341-352.
CrossRef
Google scholar
|
[90] |
VlashiE, ChenAM, BoyrieS, et al. Radiation-induced dedifferentiation of head and neck cancer cells into cancer stem cells depends on human papillomavirus status. Int J Radiat Oncol Biol Phys. 2016; 94(5):1198-1206.
CrossRef
Google scholar
|
[91] |
BastosLGR, de Marcondes PG, de-Freitas-JuniorJCM, et al. Progeny from irradiated colorectal cancer cells acquire an EMT-like phenotype and activate Wnt/β-catenin pathway. J Cell Biochem. 2014; 115(12):2175-2187.
CrossRef
Google scholar
|
[92] |
Al-AssarO, Demiciorglu F, LunardiS, et al. Contextual regulation of pancreatic cancer stem cell phenotype and radioresistance by pancreatic stellate cells. Radiother Oncol. 2014; 111(2):243-251.
CrossRef
Google scholar
|
[93] |
KimE, YounH, KwonT, et al. PAK1 tyrosine phosphorylation is required to induce epithelial–mesenchymal transition and radioresistance in lung cancer cells. Cancer Res. 2014; 74(19):5520-5531.
CrossRef
Google scholar
|
[94] |
ZengQ, LiuY, LiuJ, et al. Inhibition of ZIP4 reverses epithelial-to-mesenchymal transition and enhances the radiosensitivity in human nasopharyngeal carcinoma cells. Cell Death Dis. 2019; 10(8):588.
CrossRef
Google scholar
|
[95] |
ChangL, GrahamPH, HaoJ, et al. Emerging roles of radioresistance in prostate cancer metastasis and radiation therapy. Cancer Metastasis Rev. 2014; 33(2):469-496.
CrossRef
Google scholar
|
[96] |
DongL, ZhangX, XiangW, Ni J, ZhouW, LiH. Post-transcription mediated Snail stabilization is involved in radiation exposure induced invasion and migration of hepatocarcinoma cells. Biomed Pharmacother. 2018; 103:767-772.
CrossRef
Google scholar
|
[97] |
GuH, HuangT, ShenY, et al. Reactive oxygen species-mediated tumor microenvironment transformation: the mechanism of radioresistant gastric cancer. Oxid Med Cell Longevity. 2018; 2018(1):5801209.
CrossRef
Google scholar
|
[98] |
NakayamaA, Ninomiya I, HaradaS, et al. Metformin inhibits the radiation-induced invasive phenotype of esophageal squamous cell carcinoma. Int J Oncol. 2016; 49(5):1890-1898.
CrossRef
Google scholar
|
[99] |
LinJ-C, TsaiJ-T, ChaoT-Y, Ma H-I, LiuW-H. The STAT3/Slug axis enhances radiation-induced tumor invasion and cancer stem-like properties in radioresistant glioblastoma. Cancers. 2018; 10(12):512.
CrossRef
Google scholar
|
[100] |
KongeJ, Leteurtre F, GoislardM, et al. Breast cancer stem cell-like cells generated during TGFβ-induced EMT are radioresistant. Oncotarget. 2018; 9(34):23519-23531.
CrossRef
Google scholar
|
[101] |
Marie-EgyptienneDT, Lohse I, HillRP. Cancer stem cells, the epithelial to mesenchymal transition (EMT) and radioresistance: potential role of hypoxia. Cancer Lett. 2013; 341(1):63-72.
CrossRef
Google scholar
|
[102] |
QureshiR, AroraH, RizviMA. EMT in cervical cancer: its role in tumour progression and response to therapy. Cancer Lett. 2015; 356(2):321-331.
CrossRef
Google scholar
|
[103] |
NagarajanD, MeloT, DengZ, Almeida C, ZhaoW. ERK/GSK3β/Snail signaling mediates radiation-induced alveolar epithelial-to-mesenchymal transition. Free Radic Biol Med. 2012; 52(6):983-992.
CrossRef
Google scholar
|
[104] |
WangL, ZhaoY, XiongY, et al. K-ras mutation promotes ionizing radiation-induced invasion and migration of lung cancer in part via the cathepsin L/CUX1 pathway. Exp Cell Res. 2018; 362(2):424-435.
CrossRef
Google scholar
|
[105] |
EspinozaI, MieleL. Deadly crosstalk: Notch signaling at the intersection of EMT and cancer stem cells. Cancer Lett. 2013; 341(1):41-45.
CrossRef
Google scholar
|
[106] |
KimR-K, Kaushik N, SuhY, et al. Radiation driven epithelial-mesenchymal transition is mediated by Notch signaling in breast cancer. Oncotarget. 2016; 7(33):53430-53442.
CrossRef
Google scholar
|
[107] |
DongP, KonnoY, WatariH, Hosaka M, NoguchiM, SakuragiN. The impact of microRNA-mediated PI3K/AKT signaling on epithelial-mesenchymal transition and cancer stemness in endometrial cancer. J Transl Med. 2014; 12:231.
CrossRef
Google scholar
|
[108] |
HeY, Mingyan E, WangC, LiuG, ShiM, LiuS. CircVRK1 regulates tumor progression and radioresistance in esophageal squamous cell carcinoma by regulating miR-624-3p/PTEN/PI3K/AKT signaling pathway. Int J Biol Macromol. 2019; 125:116-123.
CrossRef
Google scholar
|
[109] |
ZhangJ, TianX-J, XingJ. Signal transduction pathways of EMT induced by TGF-β, SHH, and WNT and their crosstalks. J Clin Med. 2016; 5(4):41.
CrossRef
Google scholar
|
[110] |
CarlC, FlindtA, HartmannJ, et al. Ionizing radiation induces a motile phenotype in human carcinoma cells in vitro through hyperactivation of the TGF-beta signaling pathway. Cell Mol Life Sci. 2016; 73(2):427-443.
CrossRef
Google scholar
|
[111] |
LagadecC, VlashiE, Della DonnaL, DekmezianC, PajonkF. Radiation-induced reprogramming of breast cancer cells. Stem Cells. 2012; 30(5):833-844.
CrossRef
Google scholar
|
[112] |
ZhouS-L, ZhouZ-J, HuZ-Q, et al. CXCR2/CXCL5 axis contributes to epithelial–mesenchymal transition of HCC cells through activating PI3K/Akt/GSK-3β/Snail signaling. Cancer Lett. 2015; 358(2):124-135.
CrossRef
Google scholar
|
[113] |
WangC, LiS, LiuJ, et al. Silencing of S-phase kinase-associated protein 2 enhances radiosensitivity of esophageal cancer cells through inhibition of PI3K/AKT signaling pathway. Genomics. 2020; 112(5):3504-3510.
CrossRef
Google scholar
|
[114] |
ChoiY-J, BaekG-Y, ParkH-R, Jo S-K, JungU. Smad2/3-Regulated expression of DLX2 is associated with Radiation-Induced Epithelial-Mesenchymal transition and radioresistance of A549 and MDA-MB-231 human cancer cell lines. PLoS One. 2016; 11(1):e0147343.
CrossRef
Google scholar
|
[115] |
KimJ, KongJ, ChangH, Kim H, KimA. EGF induces epithelial-mesenchymal transition through phospho-Smad2/3-Snail signaling pathway in breast cancer cells. Oncotarget. 2016; 7(51):85021-85032.
CrossRef
Google scholar
|
[116] |
TangDG. Understanding cancer stem cell heterogeneity and plasticity. Cell Res. 2012; 22(3):457-472.
CrossRef
Google scholar
|
[117] |
VarelaI, Menendez P, Sanjuan-PlaA. Intratumoral heterogeneity and clonal evolution in blood malignancies and solid tumors. Oncotarget. 2017; 8(39):66742-66746.
CrossRef
Google scholar
|
[118] |
VermeulenL, de Sousa e Melo F, RichelDJ, MedemaJP. The developing cancer stem-cell model: clinical challenges and opportunities. Lancet Oncol. 2012; 13(2):e83-e89.
CrossRef
Google scholar
|
[119] |
TurnerC, Kohandel M. Quantitative approaches to cancer stem cells and epithelial–mesenchymal transition. Sem Cancer Biol. 2012; 22:374-378.
CrossRef
Google scholar
|
[120] |
WernerB, ScottJG, SottorivaA, Anderson ARA, TraulsenA, AltrockPM. The cancer stem cell fraction in hierarchically organized tumors can be estimated using mathematical modeling and patient-specific treatment trajectories. Cancer Res. 2016; 76(7):1705-1713.
CrossRef
Google scholar
|
[121] |
ShangS, YangC, ChenF, et al. ID1 expressing macrophages support cancer cell stemness and limit CD8+ T cell infiltration in colorectal cancer. Nat Commun. 2023; 14(1):7661.
CrossRef
Google scholar
|
[122] |
ChenX, YangM, YinJ, et al. Tumor-associated macrophages promote epithelial–mesenchymal transition and the cancer stem cell properties in triple-negative breast cancer through CCL2/AKT/β-catenin signaling. Cell Commun Signaling. 2022; 20(1):92.
CrossRef
Google scholar
|
[123] |
ZhangR, DongM, TuJ, et al. PMN-MDSCs modulated by CCL20 from cancer cells promoted breast cancer cell stemness through CXCL2-CXCR2 pathway. Signal Transduct Target Ther. 2023; 8(1):97.
CrossRef
Google scholar
|
[124] |
ZhuangJ, ShenL, LiM, et al. Cancer-associated fibroblast–derived miR-146a-5p generates a niche that promotes bladder cancer stemness and chemoresistance. Cancer Res. 2023; 83(10):1611-1627.
CrossRef
Google scholar
|
[125] |
SunL, HuangC, ZhuM, et al. Gastric cancer mesenchymal stem cells regulate PD-L1-CTCF enhancing cancer stem cell-like properties and tumorigenesis. Theranostics. 2020; 10(26):11950-11962.
CrossRef
Google scholar
|
[126] |
HeB, GaoR, LvS, et al. Cancer cell employs a microenvironmental neural signal trans-activating nucleus-mitochondria coordination to acquire stemness. Signal Transduct Target Ther. 2023; 8(1):275.
CrossRef
Google scholar
|
[127] |
KathawalaRJ, GuptaP, Ashby, Jr.,CR, ChenZ-S. The modulation of ABC transporter-mediated multidrug resistance in cancer: a review of the past decade. Drug Resist Updates. 2015; 18:1-17.
CrossRef
Google scholar
|
[128] |
HouY, ZhuQ, LiZ, et al. The FOXM1–ABCC5 axis contributes to paclitaxel resistance in nasopharyngeal carcinoma cells. Cell Death Dis. 2017; 8(3):e2659.
CrossRef
Google scholar
|
[129] |
NobiliS, Lapucci A, LandiniI, CoronnelloM, Roviello G, MiniE. Role of ATP-binding cassette transporters in cancer initiation and progression. Sem Cancer Biol. 2020; 60:72-95.
CrossRef
Google scholar
|
[130] |
WuZ-X, TengQ-X, CaiC-Y, et al. Tepotinib reverses ABCB1-mediated multidrug resistance in cancer cells. Biochem Pharmacol. 2019; 166:120-127.
CrossRef
Google scholar
|
[131] |
WangJ-Q, LiJY, TengQ-X, et al. Venetoclax, a BCL-2 inhibitor, enhances the efficacy of chemotherapeutic agents in wild-type ABCG2-overexpression-mediated MDR cancer cells. Cancers. 2020; 12(2):466.
CrossRef
Google scholar
|
[132] |
VaillantF, MerinoD, LeeL, et al. Targeting BCL-2 with the BH3 mimetic ABT-199 in estrogen receptor-positive breast cancer. Cancer Cell. 2013; 24(1):120-129.
CrossRef
Google scholar
|
[133] |
ShiotaM, Fujimoto N, ImadaK, et al. Potential role for YB-1 in castration-resistant prostate cancer and resistance to enzalutamide through the androgen receptor V7. J Natl Cancer Inst. 2016;108(7):djw005.
CrossRef
Google scholar
|
[134] |
KuwanoM, Shibata T, WatariK, OnoM. Oncogenic Y-box binding protein-1 as an effective therapeutic target in drug-resistant cancer. Cancer Sci. 2019; 110(5):1536-1543.
CrossRef
Google scholar
|
[135] |
BommertKS, Effenberger M, LeichE, et al. The feed-forward loop between YB-1 and MYC is essential for multiple myeloma cell survival. Leukemia. 2013; 27(2):441-450.
CrossRef
Google scholar
|
[136] |
KangY, HuW, IvanC, et al. Role of focal adhesion kinase in regulating YB–1–mediated paclitaxel resistance in ovarian cancer. J Natl Cancer Inst. 2013; 105(19):1485-1495.
CrossRef
Google scholar
|
[137] |
RigalliJP, Tocchetti GN, AranaMR, et al. The phytoestrogen genistein enhances multidrug resistance in breast cancer cell lines by translational regulation of ABC transporters. Cancer Lett. 2016; 376(1):165-172.
CrossRef
Google scholar
|
[138] |
LiY, LuhCJ, BurnsKA, et al. Endocrine-disrupting chemicals (EDCs): in vitro mechanism of estrogenic activation and differential effects on ER target genes. Environ Health Perspect. 2013; 121(4):459-466.
CrossRef
Google scholar
|
[139] |
RuizML, Rigalli JP, AriasA, et al. Estrogen receptor-α mediates human multidrug resistance associated protein 3 induction by 17α-ethynylestradiol. Biochem Pharmacol. 2013; 86(3):401-409.
CrossRef
Google scholar
|
[140] |
AriasA, Rigalli JP, VillanuevaSSM, et al. Regulation of expression and activity of multidrug resistance proteins MRP2 and MDR1 by estrogenic compounds in Caco-2 cells. Role in prevention of xenobiotic-induced cytotoxicity. Toxicology. 2014; 320:46-55.
CrossRef
Google scholar
|
[141] |
ChristinJR, WangC, ChungC-Y, et al. Stem cell determinant SOX9 promotes lineage plasticity and progression in basal-like breast cancer. Cell Rep. 2020; 31(10):107742.
CrossRef
Google scholar
|
[142] |
DomeniciG, Aurrekoetxea-Rodríguez I, SimõesBM, et al. A Sox2–Sox9 signalling axis maintains human breast luminal progenitor and breast cancer stem cells. Oncogene. 2019; 38(17):3151-3169.
CrossRef
Google scholar
|
[143] |
CuiJ, Christin JR, ReiszJA, et al. Targeting ABCA12-controlled ceramide homeostasis inhibits breast cancer stem cell function and chemoresistance. Sci Adv. 2023; 9(48):eadh1891.
CrossRef
Google scholar
|
[144] |
BaoL, WuJ, DodsonM, et al. ABCF2, an Nrf2 target gene, contributes to cisplatin resistance in ovarian cancer cells. Mol Carcinog. 2017; 56(6):1543-1553.
CrossRef
Google scholar
|
[145] |
SasakiN, Ishiwata T, HasegawaF, et al. Stemness and anti-cancer drug resistance in ATP-binding cassette subfamily G member 2 highly expressed pancreatic cancer is induced in 3D culture conditions. Cancer Sci. 2018; 109(4):1135-1146.
CrossRef
Google scholar
|
[146] |
PanneerselvamJ, Mohandoss P, PatelR, et al. DCLK1 regulates tumor stemness and cisplatin resistance in non-small cell lung cancer via ABCD-Member-4. Molec Ther Oncolyt. 2020; 18:24-36.
CrossRef
Google scholar
|
[147] |
JeterCR, LiuB, LiuX, et al. NANOG promotes cancer stem cell characteristics and prostate cancer resistance to androgen deprivation. Oncogene. 2011; 30(36):3833-3845.
CrossRef
Google scholar
|
[148] |
QuaziF, MoldayRS. Differential phospholipid substrates and directional transport by ATP-binding cassette proteins ABCA1, ABCA7, and ABCA4 and disease-causing mutants. J Biol Chem. 2013; 288(48):34414-34426.
CrossRef
Google scholar
|
[149] |
GuoQ, Grimmig T, GonzalezG, et al. ATP-binding cassette member B5 (ABCB5) promotes tumor cell invasiveness in human colorectal cancer. J Biol Chem. 2018; 293(28):11166-11178.
CrossRef
Google scholar
|
[150] |
ZhouS, Schuetz JD, BuntingKD, et al. The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype. Nature Med. 2001; 7(9):1028-1034.
CrossRef
Google scholar
|
[151] |
SkvortsovS, Debbage P, LukasP, SkvortsovaI. Crosstalk between DNA repair and cancer stem cell (CSC) associated intracellular pathways. Sem Cancer Biol. 2015; 31:36-42.
CrossRef
Google scholar
|
[152] |
CarruthersRD, AhmedSU, RamachandranS, et al. Replication stress drives constitutive activation of the DNA damage response and radioresistance in glioblastoma stem-like cells. Cancer Res. 2018; 78(17):5060-5071.
CrossRef
Google scholar
|
[153] |
MinW, BruhnC, GrigaraviciusP, et al. Poly (ADP-ribose) binding to Chk1 at stalled replication forks is required for S-phase checkpoint activation. Nat Commun. 2013; 4(1):2993.
CrossRef
Google scholar
|
[154] |
WangH, YangES, JiangJ, Nowsheen S, XiaF. DNA damage–induced cytotoxicity is dissociated from BRCA1’s DNA repair function but is dependent on its cytosolic accumulation. Cancer Res. 2010; 70(15):6258-6267.
CrossRef
Google scholar
|
[155] |
ZhangP, SunY, MaL. ZEB1: at the crossroads of epithelial-mesenchymal transition, metastasis and therapy resistance. Cell Cycle. 2015; 14(4):481-487.
CrossRef
Google scholar
|
[156] |
ZhangP, WeiY, WangL, et al. ATM-mediated stabilization of ZEB1 promotes DNA damage response and radioresistance through CHK1. Nature Cell Biol. 2014; 16(9):864-875.
CrossRef
Google scholar
|
[157] |
ChafferCL, Marjanovic ND, LeeT, et al. Poised chromatin at the ZEB1 promoter enables breast cancer cell plasticity and enhances tumorigenicity. Cell. 2013; 154(1):61-74.
CrossRef
Google scholar
|
[158] |
AntonelliM, Strappazzon F, ArisiI, et al. ATM kinase sustains breast cancer stem-like cells by promoting ATG4C expression and autophagy. Oncotarget. 2017; 8(13):21692-21709.
CrossRef
Google scholar
|
[159] |
McGrailDJ, LinCC-J, DaiH, et al. Defective replication stress response is inherently linked to the cancer stem cell phenotype. Cell Rep. 2018; 23(7):2095-2106.
CrossRef
Google scholar
|
[160] |
EspositoF, Giuffrida R, RacitiG, PuglisiC, ForteS. Wee1 kinase: a potential target to overcome tumor resistance to therapy. Int J Mol Sci. 2021; 22(19):10689.
CrossRef
Google scholar
|
[161] |
RedmerT, WalzI, KlingerB, et al. The role of the cancer stem cell marker CD271 in DNA damage response and drug resistance of melanoma cells. Oncogenesis. 2017; 6(1):e291.
CrossRef
Google scholar
|
[162] |
LinJ-C, TsaiJ-T, ChaoT-Y, Ma H-I, LiuW-H. The STAT3/Slug axis enhances radiation-induced tumor invasion and cancer stem-like properties in radioresistant glioblastoma. Cancers. 2018; 10(12):512.
CrossRef
Google scholar
|
[163] |
KambleD, Mahajan M, DhatR, SitasawadS. Keap1-Nrf2 pathway regulates ALDH and contributes to radioresistance in breast cancer stem cells. Cells. 2021; 10(1):83.
CrossRef
Google scholar
|
[164] |
LuY, LiangY, ZhengX, Deng X, HuangW, ZhangG. EVI1 promotes epithelial-to-mesenchymal transition, cancer stem cell features and chemo−/radioresistance in nasopharyngeal carcinoma. J Exp Clin Cancer Res. 2019; 38(1):82.
CrossRef
Google scholar
|
[165] |
Le GrandM, MukhaA, PüschelJ, et al. Interplay between MycN and c-Myc regulates radioresistance and cancer stem cell phenotype in neuroblastoma upon glutamine deprivation. Theranostics. 2020; 10(14):6411-6429.
CrossRef
Google scholar
|
[166] |
ManicG, Signore M, SistiguA, et al. CHK1-targeted therapy to deplete DNA replication-stressed, p53-deficient, hyperdiploid colorectal cancer stem cells. Gut. 2018; 67(5):903-917.
CrossRef
Google scholar
|
[167] |
Bernardino-SgherriJ, Siberchicot C, AuvréF, et al. Tumor resistance to radiotherapy is triggered by an ATM/TAK1-dependent-increased expression of the cellular prion protein. Oncogene. 2021; 40(19):3460-3469.
CrossRef
Google scholar
|
[168] |
DrápelaS, Bouchal J, JollyMK, CuligZ, Souček K. ZEB1: a critical regulator of cell plasticity, DNA damage response, and therapy resistance. Front Mol Biosci. 2020;7:36.
CrossRef
Google scholar
|
[169] |
Nolfi-DoneganD, Braganza A, ShivaS. Mitochondrial electron transport chain: oxidative phosphorylation, oxidant production, and methods of measurement. Redox Biol. 2020; 37:101674.
CrossRef
Google scholar
|
[170] |
Bayona-BafaluyMP, Montoya J, Ruiz-PesiniE. Oxidative phosphorylation system and cell culture media. Trends Cell Biol. 2021; 31(8):618-620.
CrossRef
Google scholar
|
[171] |
BianX, JiangH, MengY, Li Y, FangJ, LuZ. Regulation of gene expression by glycolytic and gluconeogenic enzymes. Trends Cell Biol. 2022; 32(9):786-799.
CrossRef
Google scholar
|
[172] |
BrunnerJS, FinleyLWS. SnapShot: cancer metabolism. Mol Cell. 2021; 81(18):3878-3878.e1.
CrossRef
Google scholar
|
[173] |
LeeSY, JeongEK, JuMK, et al. Induction of metastasis, cancer stem cell phenotype, and oncogenic metabolism in cancer cells by ionizing radiation. Mol Cancer. 2017; 16:10.
CrossRef
Google scholar
|
[174] |
RattiganKM, ZarouMM, HelgasonGV. Metabolism in stem cell–driven leukemia: parallels between hematopoiesis and immunity. Blood. 2023; 141(21):2553-2565.
|
[175] |
YangZ, ZhangC, LiuX, CheN, FengY, Xuan Y. SETD5 regulates glycolysis in breast cancer stem-like cells and fuels tumor growth. Am J Pathol. 2022; 192(4):712-721.
CrossRef
Google scholar
|
[176] |
SangR, FanR, DengA, et al. Degradation of hexokinase 2 blocks glycolysis and induces gsdme-dependent pyroptosis to amplify immunogenic cell death for breast cancer therapy. J Med Chem. 2023; 66(13):8464-8483.
CrossRef
Google scholar
|
[177] |
WangB, ZhouY, ZhangP, Li J, LuX. Solasonine inhibits cancer stemness and metastasis by modulating glucose metabolism via Wnt/β-catenin/snail pathway in osteosarcoma. Am J Chin Med. 2023; 51(05):1293-1308.
CrossRef
Google scholar
|
[178] |
ZhangY, WangY, ZhaoG, Orsulic S, MateiD. Metabolic dependencies and targets in ovarian cancer. Pharmacol Ther. 2023; 245:108413.
CrossRef
Google scholar
|
[179] |
LiuPP, LiaoJ, TangZJ, et al. Metabolic regulation of cancer cell side population by glucose through activation of the Akt pathway. Cell Death Differ. 2014; 21(1):124-135.
CrossRef
Google scholar
|
[180] |
GoidtsV, Bageritz J, PuccioL, et al. RNAi screening in glioma stem-like cells identifies PFKFB4 as a key molecule important for cancer cell survival. Oncogene. 2012; 31(27):3235-3243.
CrossRef
Google scholar
|
[181] |
HammoudiN, Riaz Ahmed KB, Garcia-PrietoC, HuangP. Metabolic alterations in cancer cells and therapeutic implications. Chin J Cancer. 2011; 30(8):508-525.
CrossRef
Google scholar
|
[182] |
EmminkBL, Verheem A, van HoudtWJ, et al. The secretome of colon cancer stem cells contains drug-metabolizing enzymes. J Proteomics. 2013; 91:84-96.
CrossRef
Google scholar
|
[183] |
LiW, LiX, WangW, et al. Tumor suppressor gene oxidored-nitro domain-containing protein 1 regulates nasopharyngeal cancer cell autophagy, metabolism, and apoptosis in vitro. Int J Biochem Cell Biol. 2013; 45(9):2016-2026.
CrossRef
Google scholar
|
[184] |
LiuG, LuoQ, LiH, LiuQ, JuY, SongG. Increased oxidative phosphorylation is required for stemness maintenance in liver cancer stem cells from hepatocellular carcinoma cell line HCCLM3 cells. Int J Mol Sci. 2020; 21(15):5276.
CrossRef
Google scholar
|
[185] |
ThirusanguP, RayU, Sarkar BhattacharyaS, et al. PFKFB3 regulates cancer stemness through the hippo pathway in small cell lung carcinoma. Oncogene. 2022; 41(33):4003-4017.
CrossRef
Google scholar
|
[186] |
BiL, RenY, FengM, et al. HDAC11 regulates glycolysis through the LKB1/AMPK signaling pathway to maintain hepatocellular carcinoma stemness. Cancer Res. 2021; 81(8):2015-2028.
CrossRef
Google scholar
|
[187] |
DongC, YuanT, WuY, et al. Loss of FBP1 by Snail-mediated repression provides metabolic advantages in basal-like breast cancer. Cancer Cell. 2013; 23(3):316-331.
CrossRef
Google scholar
|
[188] |
RoeschA, VulturA, BogeskiI, et al. Overcoming intrinsic multidrug resistance in melanoma by blocking the mitochondrial respiratory chain of slow-cycling JARID1Bhigh cells. Cancer Cell. 2013; 23(6):811-825.
CrossRef
Google scholar
|
[189] |
LagadinouED, SachA, CallahanK, et al. BCL-2 inhibition targets oxidative phosphorylation and selectively eradicates quiescent human leukemia stem cells. Cell Stem Cell. 2013; 12(3):329-341.
CrossRef
Google scholar
|
[190] |
JaniszewskaM, Suvà ML, RiggiN, et al. Imp2 controls oxidative phosphorylation and is crucial for preserving glioblastoma cancer stem cells. Genes Dev. 2012; 26(17):1926-1944.
CrossRef
Google scholar
|
[191] |
RaggiC, TaddeiML, SaccoE, et al. Mitochondrial oxidative metabolism contributes to a cancer stem cell phenotype in cholangiocarcinoma. J Hepatol. 2021; 74(6):1373-1385.
CrossRef
Google scholar
|
[192] |
VlashiE, Lagadec C, VergnesL, et al. Metabolic state of glioma stem cells and nontumorigenic cells. Proc Natl Acad Sci. 2011; 108(38):16062-16067.
CrossRef
Google scholar
|
[193] |
VlashiE, Lagadec C, VergnesL, et al. Metabolic differences in breast cancer stem cells and differentiated progeny. Breast Cancer Res Treat. 2014; 146(3):525-534.
CrossRef
Google scholar
|
[194] |
LambR, Bonuccelli G, OzsváriB, et al. Mitochondrial mass, a new metabolic biomarker for stem-like cancer cells: understanding WNT/FGF-driven anabolic signaling. Oncotarget. 2015; 6(31):30453-30471.
CrossRef
Google scholar
|
[195] |
CuyàsE, Corominas-Faja B, MenendezJA. The nutritional phenome of EMT-induced cancer stem-like cells. Oncotarget. 2014; 5(12):3970-3982.
CrossRef
Google scholar
|
[196] |
ZhangY, JiangS, HeF, et al. Single-cell transcriptomics reveals multiple chemoresistant properties in leukemic stem and progenitor cells in pediatric AML. Genome Biol. 2023; 24(1):199.
CrossRef
Google scholar
|
[197] |
FargeT, SalandE, de ToniF, et al. Chemotherapy-resistant human acute myeloid leukemia cells are not enriched for leukemic stem cells but require oxidative metabolism. Cancer Discovery. 2017; 7(7):716-735.
CrossRef
Google scholar
|
[198] |
LeeK, Giltnane JM, BalkoJM, et al. MYC and MCL1 cooperatively promote chemotherapy-resistant breast cancer stem cells via regulation of mitochondrial oxidative phosphorylation. Cell Metab. 2017; 26(4):633-647.e7.
CrossRef
Google scholar
|
[199] |
LambR, Ozsvari B, BonuccelliG, et al. Dissecting tumor metabolic heterogeneity: telomerase and large cell size metabolically define a sub-population of stem-like, mitochondrial-rich, cancer cells. Oncotarget. 2015; 6(26):21892-21905.
CrossRef
Google scholar
|
[200] |
JonesCL, Stevens BM, D’AlessandroA, et al. Inhibition of amino acid metabolism selectively targets human leukemia stem cells. Cancer Cell. 2018; 34(5):724-740.e4.
CrossRef
Google scholar
|
[201] |
AlcaláS, Villarino L, Ruiz-CañasL, et al. Targeting cancer stem cell OXPHOS with tailored ruthenium complexes as a new anti-cancer strategy. J Exp Clin Cancer Res. 2024; 43(1):33.
CrossRef
Google scholar
|
[202] |
de BeauchampL, Himonas E, HelgasonGV. Mitochondrial metabolism as a potential therapeutic target in myeloid leukaemia. Leukemia. 2022; 36(1):1-12.
CrossRef
Google scholar
|
[203] |
Peiris-PagèsM, Martinez-Outschoorn UE, PestellRG, SotgiaF, Lisanti MP. Cancer stem cell metabolism. Breast Cancer Res. 2016; 18:55.
CrossRef
Google scholar
|
[204] |
BaudotA, de la Torre V, ValenciaA. Mutated genes, pathways and processes in tumours. EMBO Rep. 2010; 11(10):805-810.
CrossRef
Google scholar
|
[205] |
LaBargeMA. The difficulty of targeting cancer stem cell niches. Clin Cancer Res. 2010; 16(12):3121-3129.
CrossRef
Google scholar
|
[206] |
AguilarE, Marin de Mas I, ZoddaE, et al. Metabolic reprogramming and dependencies associated with epithelial cancer stem cells independent of the epithelial-mesenchymal transition program. Stem Cells. 2016; 34(5):1163-1176.
CrossRef
Google scholar
|
[207] |
SosaMS, Bragado P, Aguirre-GhisoJA. Mechanisms of disseminated cancer cell dormancy: an awakening field. Nat Rev Cancer. 2014; 14(9):611-622.
CrossRef
Google scholar
|
[208] |
LouieE, NikS, ChenJ, et al. Identification of a stem-like cell population by exposing metastatic breast cancer cell lines to repetitive cycles of hypoxia and reoxygenation. Breast Cancer Res. 2010; 12(6):R94.
CrossRef
Google scholar
|
[209] |
BomkenS, Fišer K, HeidenreichO, VormoorJ. Understanding the cancer stem cell. Br J Cancer. 2010; 103(4):439-445.
CrossRef
Google scholar
|
[210] |
MedemaJP. Cancer stem cells: the challenges ahead. Nature Cell Biol. 2013; 15(4):338-344.
CrossRef
Google scholar
|
[211] |
BayikD, LathiaJD. Cancer stem cell-immune cell crosstalk in tumour progression. Nat Rev Cancer. 2021; 21(8):526-536.
CrossRef
Google scholar
|
[212] |
KrsticJ, Trivanovic D, JaukovicA, SantibanezJF, Bugarski D. Metabolic plasticity of stem cells and macrophages in cancer. Front Immunol. 2017; 8:939.
CrossRef
Google scholar
|
[213] |
MehlaK, SinghPK. Metabolic regulation of macrophage polarization in cancer. Trend Cancer. 2019; 5(12):822-834.
CrossRef
Google scholar
|
[214] |
Ricci-VitianiL, Pallini R, BiffoniM, et al. Tumour vascularization via endothelial differentiation of glioblastoma stem-like cells. Nature. 2010; 468(7325):824-828.
CrossRef
Google scholar
|
[215] |
WangR, Bhattacharya R, YeX, et al. Endothelial cells activate the cancer stem cell-associated NANOGP 8 pathway in colorectal cancer cells in a paracrine fashion. Mol Oncol. 2017; 11(8):1023-1034.
CrossRef
Google scholar
|
[216] |
LonardoE, Frias-Aldeguer J, HermannPC, HeeschenC. Pancreatic stellate cells form a niche for cancer stem cells and promote their self-renewal and invasiveness. Cell Cycle. 2012; 11(7):1282-1290.
CrossRef
Google scholar
|
[217] |
HayesJD, Dinkova-Kostova AT, TewKD. Oxidative stress in cancer. Cancer Cell. 2020; 38(2):167-197.
CrossRef
Google scholar
|
[218] |
OsukaS, Sampetrean O, ShimizuT, et al. IGF1 receptor signaling regulates adaptive radioprotection in glioma stem cells. Stem Cells. 2013; 31(4):627-640.
CrossRef
Google scholar
|
[219] |
RyooI, LeeS, KwakM-K. Redox modulating NRF2: a potential mediator of cancer stem cell resistance. Oxid Med Cell Longevity. 2016; 2016:2428153.
CrossRef
Google scholar
|
[220] |
TonelliC, ChioIIC, TuvesonDA. Transcriptional regulation by Nrf2. Antioxid Redox Signaling. 2018; 29(17):1727-1745.
CrossRef
Google scholar
|
[221] |
LuoM, BaoL, XueY, et al. ZMYND8 protects breast cancer stem cells against oxidative stress and ferroptosis through activation of NRF2. J Clin Invest. 2024; 134(6):e171166.
CrossRef
Google scholar
|
[222] |
JiangX, Stockwell BR, ConradM. Ferroptosis: mechanisms, biology and role in disease. Nat Rev Mol Cell Biol. 2021; 22(4):266-282.
CrossRef
Google scholar
|
[223] |
DongY, TuR, LiuH, QingG. Regulation of cancer cell metabolism: oncogenic MYC in the driver’s seat. Signal Transduct Target Ther. 2020; 5(1):124.
CrossRef
Google scholar
|
[224] |
DavidCJ, ChenM, AssanahM, Canoll P, ManleyJL. HnRNP proteins controlled by c-Myc deregulate pyruvate kinase mRNA splicing in cancer. Nature. 2010; 463(7279):364-368.
CrossRef
Google scholar
|
[225] |
LiY, ChenH, XieX, et al. PINK1-mediated mitophagy promotes oxidative phosphorylation and redox homeostasis to induce drug-tolerant persister cancer cells. Cancer Res. 2023; 83(3):398-413.
CrossRef
Google scholar
|
[226] |
BellHN, Rebernick RJ, GoyertJ, et al. Reuterin in the healthy gut microbiome suppresses colorectal cancer growth through altering redox balance. Cancer Cell. 2022; 40(2):185-200.e6.
CrossRef
Google scholar
|
[227] |
ZöllerM. CD44: can a cancer-initiating cell profit from an abundantly expressed molecule? Nat Rev Cancer. 2011; 11(4):254-267.
CrossRef
Google scholar
|
[228] |
TamadaM, NaganoO, TateyamaS, et al. Modulation of glucose metabolism by CD44 contributes to antioxidant status and drug resistance in cancer cells. Cancer Res. 2012; 72(6):1438-1448.
CrossRef
Google scholar
|
[229] |
KwonT, Kyung Rho J, Cheol LeeJ, et al. An important role for peroxiredoxin II in survival of A549 lung cancer cells resistant to gefitinib. Exp Mol Med. 2015; 47(5):e165.
CrossRef
Google scholar
|
[230] |
KimS-U, ParkY-H, KimJ-M, et al. Dominant role of peroxiredoxin/JNK axis in stemness regulation during neurogenesis from embryonic stem cells. Stem Cells. 2014; 32(4):998-1011.
CrossRef
Google scholar
|
[231] |
ChandimaliN, JeongDK, KwonT. Peroxiredoxin II regulates cancer stem cells and stemness-associated properties of cancers. Cancers. 2018; 10(9):305.
CrossRef
Google scholar
|
[232] |
SrinivasUS, TanBWQ, VellayappanBA, JeyasekharanAD. ROS and the DNA damage response in cancer. Redox Biol. 2019; 25:101084.
CrossRef
Google scholar
|
[233] |
HouG-X, LiuP-P, ZhangS, et al. Elimination of stem-like cancer cell side-population by auranofin through modulation of ROS and glycolysis. Cell Death Dis. 2018; 9(2):89.
CrossRef
Google scholar
|
[234] |
IannicielloA, ZarouMM, RattiganKM, et al. ULK1 inhibition promotes oxidative stress–induced differentiation and sensitizes leukemic stem cells to targeted therapy. Sci Transl Med. 2021; 13(613):eabd5016.
CrossRef
Google scholar
|
[235] |
MoW, LiuS, ZhaoX, et al. ROS scavenging nanozyme modulates immunosuppression for sensitized cancer immunotherapy. Adv Healthcare Mater. 2023; 12(21):2300191.
CrossRef
Google scholar
|
[236] |
QinS, LiB, MingH, Nice EC, ZouB, HuangC. Harnessing redox signaling to overcome therapeutic-resistant cancer dormancy. Biochim Biophys Acta Rev Cancer. 2022; 1877(4):188749.
CrossRef
Google scholar
|
[237] |
AlisonMR, GuppyNJ, LimSM, Nicholson LJ. Finding cancer stem cells: are aldehyde dehydrogenases fit for purpose? J Pathol. 2010; 222(4):335-344.
CrossRef
Google scholar
|
[238] |
ZanoniM, Bravaccini S, FabbriF, ArientiC. Emerging roles of aldehyde dehydrogenase isoforms in anti-cancer therapy resistance. Front Med. 2022; 9:795762.
CrossRef
Google scholar
|
[239] |
HolahNS, AiadHA-E-S, AsaadNY, Elkhouly EA, LasheenAG. Evaluation of the role of ALDH1 as cancer stem cell marker in colorectal carcinoma: an immunohistochemical study. J Clin Diagn Res. 2017;11(1):EC17.
|
[240] |
ZhangR, TuJ, LiuS. Novel molecular regulators of breast cancer stem cell plasticity and heterogeneity. Sem Cancer Biol. 2022; 82:11-25.
CrossRef
Google scholar
|
[241] |
Rodríguez-ZavalaJS, CallejaLF, Moreno-Sánchez R, Yoval-SánchezB. Role of aldehyde dehydrogenases in physiopathological processes. Chem Res Toxicol. 2019; 32(3):405-420.
CrossRef
Google scholar
|
[242] |
MorebJS, Muhoczy D, OstmarkB, ZucaliJR. RNAi-mediated knockdown of aldehyde dehydrogenase class-1A1 and class-3A1 is specific and reveals that each contributes equally to the resistance against 4-hydroperoxycyclophosphamide. Cancer Chemother Pharmacol. 2006; 59:127-136.
CrossRef
Google scholar
|
[243] |
van der ZeeM, Sacchetti A, CansoyM, et al. IL6/JAK1/STAT3 signaling blockade in endometrial cancer affects the ALDHhi/CD126+ stem-like component and reduces tumor burden. Cancer Res. 2015; 75(17):3608-3622.
CrossRef
Google scholar
|
[244] |
VenkataramaniV, YangY, SchubertMC, et al. Glioblastoma hijacks neuronal mechanisms for brain invasion. Cell. 2022; 185(16):2899-2917.
CrossRef
Google scholar
|
[245] |
SchaffLR, Mellinghoff IK. Glioblastoma and other primary brain malignancies in adults: a review. JAMA. 2023; 329(7):574-587.
CrossRef
Google scholar
|
[246] |
WangL, JungJ, BabikirH, et al. A single-cell Atlas of glioblastoma evolution under therapy reveals cell-intrinsic and cell-extrinsic therapeutic targets. Nature Cancer. 2022; 3(12):1534-1552.
CrossRef
Google scholar
|
[247] |
QiuZ, ZhaoL, ShenJZ, et al. Transcription elongation machinery is a druggable dependency and potentiates immunotherapy in glioblastoma stem cells. Cancer Discovery. 2022; 12(2):502-521.
CrossRef
Google scholar
|
[248] |
ChengP, WangJ, WaghmareI, et al. FOXD1–ALDH1A3 signaling is a determinant for the self-renewal and tumorigenicity of mesenchymal glioma stem cells. Cancer Res. 2016; 76(24):7219-7230.
CrossRef
Google scholar
|
[249] |
WuW, WuY, MayerK, et al. Lipid peroxidation plays an important role in chemotherapeutic effects of temozolomide and the development of therapy resistance in human glioblastoma. Transl Oncol. 2020; 13(3):100748.
CrossRef
Google scholar
|
[250] |
DinavahiSS, GowdaR, BazewiczCG, et al. Design, synthesis characterization and biological evaluation of novel multi-isoform ALDH inhibitors as potential anticancer agents. Eur J Med Chem. 2020; 187:111962.
CrossRef
Google scholar
|
[251] |
PhanTG, Croucher PI. The dormant cancer cell life cycle. Nat Rev Cancer. 2020; 20(7):398-411.
CrossRef
Google scholar
|
[252] |
YangJ, TengY. Harnessing cancer stem cell-derived exosomes to improve cancer therapy. J Exp Clin Cancer Res. 2023; 42(1):131.
CrossRef
Google scholar
|
[253] |
WuB, ZhangF, YuM, et al. Up-regulation of Anxa2 gene promotes proliferation and invasion of breast cancer MCF-7 cells. Cell Proliferation. 2012; 45(3):189-198.
CrossRef
Google scholar
|
[254] |
XuX-H, PanW, KangL-H, Feng H, SongY-Q. Association of annexin A2 with cancer development. Oncol Rep. 2015; 33(5):2121-2128.
CrossRef
Google scholar
|
[255] |
SharmaMC. Annexin A2 (ANX A2): an emerging biomarker and potential therapeutic target for aggressive cancers. Int J Cancer. 2019; 144(9):2074-2081.
CrossRef
Google scholar
|
[256] |
ChenC-Y, LinY-S, ChenC-H, Chen Y-J. Annexin A2-mediated cancer progression and therapeutic resistance in nasopharyngeal carcinoma. J Biomed Sci. 2018; 25(1):30.
CrossRef
Google scholar
|
[257] |
StaquiciniDI, RangelR, Guzman-RojasL, et al. Intracellular targeting of annexin A2 inhibits tumor cell adhesion, migration, and in vivo grafting. Sci Rep. 2017;7(1):4243.
CrossRef
Google scholar
|
[258] |
ScholzenT, GerdesJ. The Ki-67 protein: from the known and the unknown. J Cell Physiol. 2000; 182(3):311-322.
CrossRef
Google scholar
|
[259] |
GeyerFC, Rodrigues DN, WeigeltB, Reis-FilhoJS. Molecular classification of estrogen receptor-positive/luminal breast cancers. Adv Anat Pathol. 2012; 19(1):39-53.
CrossRef
Google scholar
|
[260] |
ThomasSM, SahuB, RapireddyS, et al. Antitumor effects of EGFR antisense guanidine-based peptide nucleic acids in cancer models. ACS Chem Biol. 2013; 8(2):345-352.
CrossRef
Google scholar
|
[261] |
ChengCJ, BahalR, BabarIA, et al. MicroRNA silencing for cancer therapy targeted to the tumour microenvironment. Nature. 2015; 518(7537):107-110.
CrossRef
Google scholar
|
[262] |
LiX-Q, PeiD-S, QianG-W, et al. The effect of methylated oligonucleotide targeting Ki-67 gene in human 786-0 renal carcinoma cells. Tumor Biol. 2011; 32(5):863-872.
CrossRef
Google scholar
|
[263] |
NovakD, Hüser L, EltonJJ, UmanskyV, Altevogt P, UtikalJ. SOX2 in development and cancer biology. Sem Cancer Biol. 2020; 67:74-82.
CrossRef
Google scholar
|
[264] |
TanS, Guschin D, DavalosA, et al. Zinc-finger protein-targeted gene regulation: genomewide single-gene specificity. Proc Natl Acad Sci. 2003; 100(21):11997-12002.
CrossRef
Google scholar
|
[265] |
YokotaE, Yamatsuji T, TakaokaM, et al. Targeted silencing of SOX2 by an artificial transcription factor showed antitumor effect in lung and esophageal squamous cell carcinoma. Oncotarget. 2017; 8(61):103063-103076.
CrossRef
Google scholar
|
[266] |
WangR-F, WangHY. Immune targets and neoantigens for cancer immunotherapy and precision medicine. Cell Res. 2017; 27(1):11-37.
CrossRef
Google scholar
|
[267] |
SadelainM. CAR therapy: the CD19 paradigm. J Clin Invest. 2015; 125(9):3392-3400.
CrossRef
Google scholar
|
[268] |
MaudeSL, FreyN, ShawPA, et al. Chimeric antigen receptor T cells for sustained remissions in leukemia. N Engl J Med. 2014; 371(16):1507-1517.
CrossRef
Google scholar
|
[269] |
SternerRC, Sterner RM. CAR-T cell therapy: current limitations and potential strategies. Blood Cancer J. 2021; 11(4):69.
CrossRef
Google scholar
|
[270] |
KlebanoffCA, Rosenberg SA, RestifoNP. Prospects for gene-engineered T cell immunotherapy for solid cancers. Nature Med. 2016; 22(1):26-36.
CrossRef
Google scholar
|
[271] |
RobbinsPF, MorganRA, FeldmanSA, et al. Tumor regression in patients with metastatic synovial cell sarcoma and melanoma using genetically engineered lymphocytes reactive with NY-ESO-1. J Clin Oncol. 2011; 29(7):917-924.
CrossRef
Google scholar
|
[272] |
RapoportAP, Stadtmauer EA, Binder-SchollGK, et al. NY-ESO-1–specific TCR–engineered T cells mediate sustained antigen-specific antitumor effects in myeloma. Nature Med. 2015; 21(8):914-921.
CrossRef
Google scholar
|
[273] |
TanKX, Danquah MK, SidhuA, OngkudonCM, LauSY. Towards targeted cancer therapy: Aptamer or oncolytic virus? Eur J Pharm Sci. 2017;96:8-19.
CrossRef
Google scholar
|
[274] |
ZhangY, WangX. Targeting the Wnt/β-catenin signaling pathway in cancer. J Hematol Oncol. 2020; 13(1):165.
CrossRef
Google scholar
|
[275] |
LiuX, SuK, SunX, et al. Sec62 promotes stemness and chemoresistance of human colorectal cancer through activating Wnt/β-catenin pathway. J Exp Clin Cancer Res. 2021; 40:132.
CrossRef
Google scholar
|
[276] |
ManniW, MinW. Signaling pathways in the regulation of cancer stem cells and associated targeted therapy. MedComm. 2022; 3(4):e176.
CrossRef
Google scholar
|
[277] |
Da CostaKM, Freire-de-Lima L, Da FonsecaLM, PreviatoJO, Mendonça-Previato L, ValenteRC. ABCB1 and ABCC1 function during TGF-β-induced epithelial-mesenchymal transition: relationship between multidrug resistance and tumor progression. Int J Mol Sci. 2023; 24(7):6046.
CrossRef
Google scholar
|
[278] |
AlzahraniAS. PI3K/Akt/mTOR inhibitors in cancer: at the bench and bedside. Sem Cancer Biol. 2019; 59:125-132.
CrossRef
Google scholar
|
[279] |
HerN-H, JeongS-I, ChoK, et al. PPARδ promotes oncogenic redirection of TGF-β1 signaling through the activation of the ABCA1-Cav1 pathway. Cell Cycle. 2013; 12(10):1521-1535.
CrossRef
Google scholar
|
[280] |
DerynckR, TurleySJ, AkhurstRJ. TGFβ biology in cancer progression and immunotherapy. Nat Rev Clin Oncol. 2021; 18(1):9-34.
CrossRef
Google scholar
|
[281] |
ZhangL, WangY, XiaT, et al. Suppression for lung metastasis by depletion of collagen I and lysyl oxidase via losartan assisted with paclitaxel-loaded pH-sensitive liposomes in breast cancer. Drug Delivery. 2016; 23(8):2970-2979.
CrossRef
Google scholar
|
[282] |
ChenC-L, Tsukamoto H, LiuJ-C, et al. Reciprocal regulation by TLR4 and TGF-β in tumor-initiating stem-like cells. J Clin Invest. 2013; 123(7):2832-2849.
CrossRef
Google scholar
|
[283] |
AdachiK, KoppW, WuG, et al. ESRRB unlocks silenced enhancers for reprogramming to naive pluripotency. Cell Stem Cell. 2018; 23(2):266-275.e6.
CrossRef
Google scholar
|
[284] |
LiQ-S, ZhengP-S. ESRRB inhibits the TGFβ signaling pathway to drive cell proliferation in cervical cancer. Cancer Res. 2023; 83(18):3095-3114.
CrossRef
Google scholar
|
[285] |
WuC-P, HungC-Y, LusvarghiS, et al. Overexpression of ABCB1 and ABCG2 contributes to reduced efficacy of the PI3K/mTOR inhibitor samotolisib (LY3023414) in cancer cell lines. Biochem Pharmacol. 2020; 180:114137.
CrossRef
Google scholar
|
[286] |
ZhangD, DengY, KukanjaP, et al. Spatial epigenome–transcriptome co-profiling of mammalian tissues. Nature. 2023; 616(7955):113-122.
CrossRef
Google scholar
|
[287] |
GongF, ChiuL-Y, MillerKM. Acetylation reader proteins: linking acetylation signaling to genome maintenance and cancer. PLoS Genet. 2016; 12(9):e1006272.
CrossRef
Google scholar
|
[288] |
PramanikD, Campbell NR, KarikariC, et al. Restitution of tumor suppressor microRNAs using a systemic nanovector inhibits pancreatic cancer growth in mice. Mol Cancer Ther. 2011; 10(8):1470-1480.
CrossRef
Google scholar
|
[289] |
FergusonLP, DiazE, ReyaT. The role of the microenvironment and immune system in regulating stem cell fate in cancer. Trend Cancer. 2021; 7(7):624-634.
CrossRef
Google scholar
|
[290] |
YuanS, Stewart KS, YangY, et al. Ras drives malignancy through stem cell crosstalk with the microenvironment. Nature. 2022; 612(7940):555-563.
CrossRef
Google scholar
|
[291] |
ZhangY, YangJ, BronzeMS, Houchen CW, LiM. Interplay of tumor microenvironment factors and cancer stem cell enrichment in pancreatic ductal adenocarcinoma. Gastroenterology. 2021; 161(6):1800-1802.
CrossRef
Google scholar
|
[292] |
WigerupC, Påhlman S, BexellD. Therapeutic targeting of hypoxia and hypoxia-inducible factors in cancer. Pharmacol Ther. 2016; 164:152-169.
CrossRef
Google scholar
|
[293] |
RankinEB, NamJM, GiacciaAJ. Hypoxia: signaling the metastatic cascade. Trend Cancer. 2016; 2(6):295-304.
CrossRef
Google scholar
|
[294] |
LeeSY, JeonHM, JuMK, et al. Dlx-2 is implicated in TGF-β-and Wnt-induced epithelial-mesenchymal, glycolytic switch, and mitochondrial repression by Snail activation. Int J Oncol. 2015; 46(4):1768-1780.
CrossRef
Google scholar
|
[295] |
OhshioY, Hanaoka J, KontaniK, TeramotoK. Tranilast inhibits the function of cancer-associated fibroblasts responsible for the induction of immune suppressor cell types. Scand J Immunol. 2014; 80(6):408-416.
CrossRef
Google scholar
|
[296] |
Mediavilla-VarelaM, Boateng K, NoyesD, AntoniaSJ. The anti-fibrotic agent pirfenidone synergizes with cisplatin in killing tumor cells and cancer-associated fibroblasts. BMC Cancer. 2016; 16(1):176.
CrossRef
Google scholar
|
[297] |
HuC, LiuX, RanW, et al. Regulating cancer associated fibroblasts with losartan-loaded injectable peptide hydrogel to potentiate chemotherapy in inhibiting growth and lung metastasis of triple negative breast cancer. Biomaterials. 2017; 144:60-72.
CrossRef
Google scholar
|
[298] |
KeshK, GuptaVK, DurdenB, et al. Therapy resistance, cancer stem cells and ECM in cancer: the matrix reloaded. Cancers. 2020; 12(10):3067.
CrossRef
Google scholar
|
[299] |
YanY, ZuoX, WeiD. Concise review: emerging role of CD44 in cancer stem cells: A promising biomarker and therapeutic target. Stem Cells Transl Med. 2015; 4(9):1033-1043.
CrossRef
Google scholar
|
[300] |
ThapaR, WilsonGD. The importance of CD44 as a stem cell biomarker and therapeutic target in cancer. Stem Cells Int. 2016; 2016(1):2087204.
CrossRef
Google scholar
|
[301] |
ChoiKY, ChungH, MinKH, et al. Self-assembled hyaluronic acid nanoparticles for active tumor targeting. Biomaterials. 2010; 31(1):106-114.
CrossRef
Google scholar
|
[302] |
YangC, HeY, ZhangH, et al. Selective killing of breast cancer cells expressing activated CD44 using CD44 ligand-coated nanoparticles in vitro and in vivo. Oncotarget. 2015; 6(17):15283-15296.
CrossRef
Google scholar
|
[303] |
WangH, Agarwal P, ZhaoS, et al. Hyaluronic acid-decorated dual responsive nanoparticles of pluronic F127, PLGA, and chitosan for targeted co-delivery of doxorubicin and irinotecan to eliminate cancer stem-like cells. Biomaterials. 2015; 72:74-89.
CrossRef
Google scholar
|
[304] |
ShenY, LiW. HA/HSA co-modified erlotinib–albumin nanoparticles for lung cancer treatment. Drug Des Devel Ther. 2018; 12:2285.
CrossRef
Google scholar
|
[305] |
BacharG, CohenK, HodR, et al. Hyaluronan-grafted particle clusters loaded with Mitomycin C as selective nanovectors for primary head and neck cancers. Biomaterials. 2011; 32(21):4840-4848.
CrossRef
Google scholar
|
[306] |
KesharwaniP, Banerjee S, PadhyeS, SarkarFH, IyerAK. Hyaluronic acid engineered nanomicelles loaded with 3, 4-difluorobenzylidene curcumin for targeted killing of CD44+ stem-like pancreatic cancer cells. Biomacromolecules. 2015; 16(9):3042-3053.
CrossRef
Google scholar
|
[307] |
SohelM, IslamMN, HossainMA, et al. Pharmacological properties to pharmacological insight of sesamin in breast cancer treatment: a literature-based review study. Int J Breast Cancer. 2022; 2022:1-13.
CrossRef
Google scholar
|
[308] |
MajdalawiehAF, MassriM, NasrallahGK. A comprehensive review on the anti-cancer properties and mechanisms of action of sesamin, a lignan in sesame seeds (Sesamum indicum). Eur J Pharmacol. 2017; 815:512-521.
CrossRef
Google scholar
|
[309] |
LiuX, ZhangY, LiY, et al. Development of hedgehog pathway inhibitors by epigenetically targeting GLI through BET bromodomain for the treatment of medulloblastoma. Acta Pharm Sin B. 2021; 11(2):488-504.
CrossRef
Google scholar
|
[310] |
TongW, QiuL, QiM, et al. GANT-61 and GDC-0449 induce apoptosis of prostate cancer stem cells through a GLI-dependent mechanism. J Cell Biochem. 2018; 119(4):3641-3652.
CrossRef
Google scholar
|
[311] |
TylawskyDE, Kiguchi H, VaynshteynJ, et al. P-selectin-targeted nanocarriers induce active crossing of the blood–brain barrier via caveolin-1-dependent transcytosis. Nat Mater. 2023; 22(3):391-399.
CrossRef
Google scholar
|
[312] |
YanR, ZhuH, HuangP, et al. Liquidambaric acid inhibits Wnt/β-catenin signaling and colon cancer via targeting TNF receptor-associated factor 2. Cell Rep. 2022; 38(5):110319.
CrossRef
Google scholar
|
[313] |
MuR, SunH, ZengY, et al. Nanomodulators targeting endothelial WNT and pericytes to reversibly open the blood–tumor barrier for boosted brain tumor therapy. J Controlled Release. 2024; 369:458-474.
CrossRef
Google scholar
|
[314] |
SabolHM, Ferrari AJ, AdhikariM, et al. Targeting notch inhibitors to the myeloma bone marrow niche decreases tumor growth and bone destruction without gut toxicity. Cancer Res. 2021; 81(19):5102-5114.
CrossRef
Google scholar
|
[315] |
HanQ, XieQR, LiF, et al. Targeted inhibition of SIRT6 via engineered exosomes impairs tumorigenesis and metastasis in prostate cancer. Theranostics. 2021; 11(13):6526-6541.
CrossRef
Google scholar
|
[316] |
TewariAB, SainiA, SharmaD. Extirpating the cancer stem cell hydra: differentiation therapy and hyperthermia therapy for targeting the cancer stem cell hierarchy. Clin Exp Med. 2023; 23:3125-3145.
CrossRef
Google scholar
|
[317] |
MassardC, Deutsch E, SoriaJ-C. Tumour stem cell-targeted treatment: elimination or differentiation. Ann Oncol. 2006; 17(11):1620-1624.
CrossRef
Google scholar
|
[318] |
SoriaJ-C, KimES, FayetteJ, Lantuejoul S, DeutschE, HongWK. Chemoprevention of lung cancer. Lancet Oncol. 2003; 4(11):659-669.
CrossRef
Google scholar
|
[319] |
ArimaY, Nobusue H, SayaH. Targeting of cancer stem cells by differentiation therapy. Cancer Sci. 2020; 111(8):2689-2695.
CrossRef
Google scholar
|
[320] |
ZhouH-M, ZhangJ-G, ZhangX, Li Q. Targeting cancer stem cells for reversing therapy resistance: mechanism, signaling, and prospective agents. Signal Transduct Target Ther. 2021; 6(1):62.
CrossRef
Google scholar
|
[321] |
TallmanMS, Andersen JW, SchifferCA, et al. All-trans retinoic acid in acute promyelocytic leukemia: long-term outcome and prognostic factor analysis from the North American Intergroup protocol: Presented in part at the 39th meeting of the American Society of Hematology, New Orleans, LA, December 1999. Blood. 2002;100(13):4298-4302.
CrossRef
Google scholar
|
[322] |
Dela CruzF, Matushansky I. Solid tumor differentiation therapy—is it possible? Oncotarget. 2012; 3(5):559-567.
CrossRef
Google scholar
|
[323] |
Lo-CocoF, Avvisati G, VignettiM, et al. Retinoic acid and arsenic trioxide for acute promyelocytic leukemia. N Engl J Med. 2013; 369:111-121.
CrossRef
Google scholar
|
[324] |
Dos SantosGA, KatsL, PandolfiPP. Synergy against PML-RARa: targeting transcription, proteolysis, differentiation, and self-renewal in acute promyelocytic leukemia. J Exp Med. 2013; 210(13):2793-2802.
CrossRef
Google scholar
|
[325] |
MartensJHA, Brinkman AB, SimmerF, et al. PML-RARα/RXR alters the epigenetic landscape in acute promyelocytic leukemia. Cancer Cell. 2010; 17(2):173-185.
CrossRef
Google scholar
|
[326] |
Vitaliano-PrunierA, Halftermeyer J, AblainJ, et al. Clearance of PML/RARA-bound promoters suffice to initiate APL differentiation. Blood. 2014; 124(25):3772-3780.
CrossRef
Google scholar
|
[327] |
AblainJ, LeivaM, PeresL, Fonsart J, AnthonyE, de ThéH. Uncoupling RARA transcriptional activation and degradation clarifies the bases for APL response to therapies. J Exp Med. 2013; 210(4):647-653.
CrossRef
Google scholar
|
[328] |
BernardiR, Pandolfi PP. Structure, dynamics and functions of promyelocytic leukaemia nuclear bodies. Nat Rev Mol Cell Biol. 2007; 8(12):1006-1016.
CrossRef
Google scholar
|
[329] |
AblainJ, RiceK, SoilihiH, de Reynies A, MinucciS, de ThéH. Activation of a promyelocytic leukemia–tumor protein 53 axis underlies acute promyelocytic leukemia cure. Nature Med. 2014; 20(2):167-174.
CrossRef
Google scholar
|
[330] |
RobozGJ, DiNardo CD, SteinEM, et al. Ivosidenib induces deep durable remissions in patients with newly diagnosed IDH1-mutant acute myeloid leukemia. Blood. 2020; 135(7):463-471.
CrossRef
Google scholar
|
[331] |
PollyeaDA, Tallman MS, de BottonS, et al. Enasidenib, an inhibitor of mutant IDH2 proteins, induces durable remissions in older patients with newly diagnosed acute myeloid leukemia. Leukemia. 2019; 33(11):2575-2584.
CrossRef
Google scholar
|
[332] |
LosmanJ-A, KaelinWG. What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer. Genes Dev. 2013; 27(8):836-852.
CrossRef
Google scholar
|
[333] |
MolenaarRJ, Maciejewski JP, WilminkJW, van NoordenCJF. Wild-type and mutated IDH1/2 enzymes and therapy responses. Oncogene. 2018; 37(15):1949-1960.
CrossRef
Google scholar
|
[334] |
MukherjeeJ, Johannessen T-C, OhbaS, et al. Mutant IDH1 cooperates with ATRX loss to drive the alternative lengthening of telomere phenotype in glioma. Cancer Res. 2018; 78(11):2966-2977.
CrossRef
Google scholar
|
[335] |
ZhangX, WangX, WangXQD, et al. Dnmt3a loss and Idh2 neomorphic mutations mutually potentiate malignant hematopoiesis. Blood. 2020; 135(11):845-856.
CrossRef
Google scholar
|
[336] |
LosmanJ-A, LooperRE, KoivunenP, et al. (R)-2-hydroxyglutarate is sufficient to promote leukemogenesis and its effects are reversible. Science. 2013; 339(6127):1621-1625.
CrossRef
Google scholar
|
[337] |
KatsLM, Vervoort SJ, ColeR, et al. A pharmacogenomic approach validates AG-221 as an effective and on-target therapy in IDH2 mutant AML. Leukemia. 2017; 31(6):1466-1470.
CrossRef
Google scholar
|
[338] |
QuekL, DavidMD, KennedyA, et al. Clonal heterogeneity of acute myeloid leukemia treated with the IDH2 inhibitor enasidenib. Nature Med. 2018; 24(8):1167-1177.
CrossRef
Google scholar
|
[339] |
ChenY, CaoJ, ZhangN, et al. Advances in differentiation therapy for osteosarcoma. Drug Discovery Today. 2020; 25(3):497-504.
CrossRef
Google scholar
|
[340] |
HeB-C, ChenL, ZuoG-W, et al. Synergistic antitumor effect of the activated PPARγ and retinoid receptors on human osteosarcoma. Clin Cancer Res. 2010; 16(8):2235-2245.
CrossRef
Google scholar
|
[341] |
ZhuangH, ZhangX, ZhuC, et al. Molecular mechanisms of PPAR-γ governing MSC osteogenic and adipogenic differentiation. Curr Stem Cell Res Ther. 2016; 11(3):255-264.
CrossRef
Google scholar
|
[342] |
LuoX, ChenJ, SongW-X, et al. Osteogenic BMPs promote tumor growth of human osteosarcomas that harbor differentiation defects. Lab Invest. 2008; 88(12):1264-1277.
CrossRef
Google scholar
|
[343] |
SongM, TianX, LuM, et al. Genistein exerts growth inhibition on human osteosarcoma MG-63 cells via PPARγ pathway. Int J Oncol. 2015; 46(3):1131-1140.
CrossRef
Google scholar
|
[344] |
LuY, SunY, ZhuJ, et al. Oridonin exerts anticancer effect on osteosarcoma by activating PPAR-γ and inhibiting Nrf2 pathway. Cell Death Dis. 2018; 9(1):15.
CrossRef
Google scholar
|
[345] |
KhalidAB, KrumSA. Estrogen receptors alpha and beta in bone. Bone. 2016; 87:130-135.
CrossRef
Google scholar
|
[346] |
KrumSA. Direct transcriptional targets of sex steroid hormones in bone. J Cell Biochem. 2011; 112(2):401-408.
CrossRef
Google scholar
|
[347] |
Lillo OsunaMA, Garcia-Lopez J, El AyachiI, et al. Activation of estrogen receptor alpha by decitabine inhibits osteosarcoma growth and metastasis. Cancer Res. 2019; 79(6):1054-1068.
CrossRef
Google scholar
|
[348] |
LeeC-H, HuangY-L, LiaoJ-F, Chiou W-F. Ugonin k-stimulated osteogenesis involves estrogen receptor-dependent activation of non-classical Src signaling pathway and classical pathway. Eur J Pharmacol. 2012;676(1-3):26-33.
CrossRef
Google scholar
|
[349] |
PangX-G, CongY, BaoN-R, Li Y-G, ZhaoJ-N. Quercetin stimulates bone marrow mesenchymal stem cell differentiation through an estrogen receptor-mediated pathway. BioMed Res Int. 2018; 2018(1):1-11.
CrossRef
Google scholar
|
[350] |
TiroshI, IzarB, PrakadanSM, et al. Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq. Science. 2016; 352(6282):189-196.
CrossRef
Google scholar
|
[351] |
TrapnellC, Cacchiarelli D, GrimsbyJ, et al. The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells. Nature Biotechnol. 2014; 32(4):381-386.
CrossRef
Google scholar
|
[352] |
JanuchowskiR, Wojtowicz K, ZabelM. The role of aldehyde dehydrogenase (ALDH) in cancer drug resistance. Biomed Pharmacother. 2013; 67(7):669-680.
CrossRef
Google scholar
|
[353] |
DavidKA, MonganNP, SmithC, Gudas LJ, NanusD. Phase I trial of ATRA-IV and Depakote in patients with advanced solid tumor malignancies. Cancer Biol Ther. 2010; 9(9):678-684.
CrossRef
Google scholar
|
[354] |
RoyR, WillanP, ClarkeR, Farnie G. Differentiation therapy: targeting breast cancer stem cells to reduce resistance to radiotherapy and chemotherapy. Breast Cancer Res. 2010;12(1):O5.
CrossRef
Google scholar
|
[355] |
PetitC, LacasB, PignonJ-P, et al. Chemotherapy and radiotherapy in locally advanced head and neck cancer: an individual patient data network meta-analysis. Lancet Oncol. 2021; 22(5):727-736.
CrossRef
Google scholar
|
[356] |
PetitC, LeeA, MaJ, et al. Role of chemotherapy in patients with nasopharynx carcinoma treated with radiotherapy (MAC-NPC): an updated individual patient data network meta-analysis. Lancet Oncol. 2023; 24(6):611-623.
CrossRef
Google scholar
|
[357] |
AgudaBD. Modeling microRNA-transcription factor networks in cancer. MicroRNA Cancer Regulation. 2013; 774:149-167.
CrossRef
Google scholar
|
[358] |
HatziapostolouM, Polytarchou C, AggelidouE, et al. An HNF4α-miRNA inflammatory feedback circuit regulates hepatocellular oncogenesis. Cell. 2011; 147(6):1233-1247.
CrossRef
Google scholar
|
[359] |
LandaI, Ibrahimpasic T, BoucaiL, et al. Genomic and transcriptomic hallmarks of poorly differentiated and anaplastic thyroid cancers. J Clin Invest. 2016; 126(3):1052-1066.
CrossRef
Google scholar
|
[360] |
DettmerM, Schmitt A, SteinertH, MochH, Komminoth P, PerrenA. Poorly differentiated oncocytic thyroid carcinoma–diagnostic implications and outcome. Histopathology. 2012; 60(7):1045-1051.
CrossRef
Google scholar
|
[361] |
GraweF, CahyaA, FabritiusMP, et al. Course of disease and clinical management of patients with poorly differentiated thyroid carcinoma. Cancers. 2021; 13(21):5309.
CrossRef
Google scholar
|
[362] |
YangH, ChenZ, WuM, LeiT, YuH, GeM. Remarkable response in 2 cases of advanced poorly differentiated thyroid carcinoma with liposomal doxorubicin plus cisplatin. Cancer Biol Ther. 2016; 17(6):693-697.
CrossRef
Google scholar
|
[363] |
BroseMS, Nutting CM, JarzabB, et al. Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial. The Lancet. 2014; 384(9940):319-328.
CrossRef
Google scholar
|
[364] |
SchlumbergerM, TaharaM, WirthLJ, et al. Lenvatinib versus placebo in radioiodine-refractory thyroid cancer. N Engl J Med. 2015; 372(7):621-630.
CrossRef
Google scholar
|
[365] |
ViolaD, Valerio L, MolinaroE, et al. Treatment of advanced thyroid cancer with targeted therapies: ten years of experience. Endocr Relat Cancer. 2016;23(4):R185-R205.
CrossRef
Google scholar
|
[366] |
AntonelliM, RasoA, MascelliS, et al. SMARCB1/INI1 involvement in pediatric chordoma. Am J Surg Pathol. 2017; 41(1):56-61.
CrossRef
Google scholar
|
[367] |
BishopJA, Antonescu CR, WestraWH. SMARCB1 (INI-1) deficient carcinomas of the sinonasal tract. Am J Surg Pathol. 2014; 38(9):1282-1289.
CrossRef
Google scholar
|
[368] |
HasselblattM, ThomasC, HovestadtV, et al. Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis. Acta Neuropathol. 2016; 132(1):149-151.
CrossRef
Google scholar
|
[369] |
RenardC, Pissaloux D, DecouvelaereAV, BourdeautF, Ranchère D. Non-rhabdoid pediatric SMARCB1-deficient tumors: overlap between chordomas and malignant rhabdoid tumors? Cancer Genetics. 2014; 207(9):384-389.
CrossRef
Google scholar
|
[370] |
StacchiottiS, CasaliPG. Systemic therapy options for unresectable and metastatic chordomas. Curr Oncol Rep. 2011; 13(4):323-330.
CrossRef
Google scholar
|
[371] |
ChenY-L, Liebsch N, KobayashiW, et al. Definitive high-dose photon/proton radiotherapy for unresected mobile spine and sacral chordomas. Spine. 2013;38(15):E930-E936.
CrossRef
Google scholar
|
[372] |
StacchiottiS, LonghiA, FerraresiV, et al. Phase II study of imatinib in advanced chordoma. J Clin Oncol. 2012; 30(9):914-920.
CrossRef
Google scholar
|
[373] |
StacchiottiS, Tamborini E, Lo VulloS, et al. Phase II study on lapatinib in advanced EGFR-positive chordoma. Ann Oncol. 2013; 24(7):1931-1936.
CrossRef
Google scholar
|
[374] |
Al-RahawanMM, Siebert JD, MitchellCS, SmithSD. Durable complete response to chemotherapy in an infant with a clival chordoma. Pediatr Blood Cancer. 2012; 59(2):323-325.
CrossRef
Google scholar
|
[375] |
LiuT-C, Hamilton N, HawkinsW, GaoF, CaoD. Comparison of WHO classifications (2004, 2010), the Hochwald grading system, and AJCC and ENETS staging systems in predicting prognosis in locoregional well-differentiated pancreatic neuroendocrine tumors. Am J Surg Pathol. 2013; 37(6):853-859.
CrossRef
Google scholar
|
[376] |
TangLH, UntchBR, ReidyDL, et al. Well-differentiated neuroendocrine tumors with a morphologically apparent high-grade component: a pathway distinct from poorly differentiated neuroendocrine carcinomas. Clin Cancer Res. 2016; 22(4):1011-1017.
CrossRef
Google scholar
|
[377] |
LynchTJ, Bondarenko I, LuftA, et al. Ipilimumab in combination with paclitaxel and carboplatin as first-line treatment in stage IIIB/IV non–small-cell lung cancer: results from a randomized, double-blind, multicenter phase II study. J Clin Oncol. 2012; 30(17):2046-2054.
CrossRef
Google scholar
|
[378] |
HookKE, GarzaSJ, LiraME, et al. An integrated genomic approach to identify predictive biomarkers of response to the aurora kinase inhibitor PF-03814735. Mol Cancer Ther. 2012; 11(3):710-719.
CrossRef
Google scholar
|
[379] |
SosML, Dietlein F, PeiferM, et al. A framework for identification of actionable cancer genome dependencies in small cell lung cancer. Proc Natl Acad Sci. 2012; 109(42):17034-17039.
CrossRef
Google scholar
|
[380] |
MollaogluG, Guthrie MR, BöhmS, et al. MYC drives progression of small cell lung cancer to a variant neuroendocrine subtype with vulnerability to aurora kinase inhibition. Cancer Cell. 2017; 31(2):270-285.
CrossRef
Google scholar
|
[381] |
JahchanNS, LimJS, BolaB, et al. Identification and targeting of long-term tumor-propagating cells in small cell lung cancer. Cell Rep. 2016; 16(3):644-656.
CrossRef
Google scholar
|
[382] |
TsangSV, Rainusso N, LiuM, et al. LncRNA PVT-1 promotes osteosarcoma cancer stem-like properties through direct interaction with TRIM28 and TSC2 ubiquitination. Oncogene. 2022; 41(50):5373-5384.
CrossRef
Google scholar
|
[383] |
TornínJ, Mateu-Sanz M, ReyV, et al. Cold plasma and inhibition of STAT3 selectively target tumorigenicity in osteosarcoma. Redox Biol. 2023; 62:102685.
CrossRef
Google scholar
|
[384] |
FatmaH, Siddique HR. Pluripotency inducing Yamanaka factors: role in stemness and chemoresistance of liver cancer. Expert Rev Anticancer Ther. 2021; 21(8):853-864.
CrossRef
Google scholar
|
[385] |
MohiuddinIS, WeiS-J, KangMH. Role of OCT4 in cancer stem-like cells and chemotherapy resistance. Biochim Biophys Acta Mol Basis Dis. 2020; 1866(4):165432.
CrossRef
Google scholar
|
[386] |
LeiZ-N, TianQ, TengQ-X, et al. Understanding and targeting resistance mechanisms in cancer. MedComm. 2023; 4(3):e265.
CrossRef
Google scholar
|
[387] |
ZhangL, ChenW, LiuS, ChenC. Targeting breast cancer stem cells. Int J Biol Sci. 2023; 19(2):552-570.
CrossRef
Google scholar
|
[388] |
ZhangZ, QinS, ChenY, et al. Inhibition of NPC1L1 disrupts adaptive responses of drug-tolerant persister cells to chemotherapy. EMBO Mol Med. 2022; 14:e14903.
CrossRef
Google scholar
|
[389] |
WangH, GongP, ChenT, et al. Colorectal cancer stem cell states uncovered by simultaneous single-cell analysis of transcriptome and telomeres. Adv Sci. 2021; 8(8):2004320.
CrossRef
Google scholar
|
[390] |
ZhengH, PomyenY, HernandezMO, et al. Single-cell analysis reveals cancer stem cell heterogeneity in hepatocellular carcinoma. Hepatology. 2018; 68(1):127-140.
CrossRef
Google scholar
|
[391] |
BurguinA, DiorioC, DurocherF. Breast cancer treatments: updates and new challenges. J Pers Med. 2021; 11(8):808.
CrossRef
Google scholar
|
[392] |
LathiaJD, MackSC, Mulkearns-HubertEE, ValentimCLL, RichJN. Cancer stem cells in glioblastoma. Genes Dev. 2015; 29(12):1203-1217.
CrossRef
Google scholar
|
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