Reactive oxygen species generation is essential for cisplatin-induced accelerated senescence in hepatocellular carcinoma

Frontiers of Medicine ›› 2014, Vol. 8 ›› Issue (2) : 227-235.

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Frontiers of Medicine ›› 2014, Vol. 8 ›› Issue (2) : 227-235. DOI: 10.1007/s11684-014-0327-1
RESEARCH ARTICLE

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Reactive oxygen species generation is essential for cisplatin-induced accelerated senescence in hepatocellular carcinoma

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Abstract

Accelerated senescence is important because this process is involved in tumor suppression and has been induced by many chemotherapeutic agents. The platinum-based chemotherapeutic agent cisplatin displays a wide range of antitumor activities. However, the molecular mechanism of cisplatin-induced accelerated senescence in hepatocellular carcinoma (HCC) remains unclear. In the present study, the growth inhibitory effect of cisplatin on HepG2 and SMMC-7721 cells was detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Cellular senescence was then assessed by β-galactosidase assay. Senescence-related factors, including p53, p21, and p16, were evaluated by quantitative reverse transcription-polymerase chain reaction. Reactive oxygen species (ROS) was analyzed by flow cytometry. Our results revealed that cisplatin reduced the proliferation of HepG2 and SMMC-7721 cells in a dose- and time-dependent manner. Senescent phenotype observed in cisplatin-treated hepatoma cells was dependent on p53 and p21 activation but not on p16 activation. Furthermore, cisplatin-induced accelerated senescence depended on intracellular ROS generation. The ROS scavenger N-acetyl-L-cysteine also significantly suppressed the cisplatin-induced senescence of HepG2 and SMMC-7721 cells. In conclusion, our results revealed a functional link between intracellular ROS generation and cisplatin-induced accelerated senescence, and this link may be used as a potential target of HCC.

Keywords

reactive oxygen species / senescence / cisplatin / hepatocellular carcinoma

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. . Frontiers of Medicine. 2014, 8(2): 227-235 https://doi.org/10.1007/s11684-014-0327-1

参考文献

[1]
HayflickL. The limited in vitro lifetime of human diploid cell strains. Exp Cell Res1965; 37(3): 614-636
CrossRef ADS Pubmed Google scholar
[2]
DimriGP, LeeX, BasileG, AcostaM, ScottG, RoskelleyC, MedranoEE, LinskensM, RubeljI, Pereira-SmithO. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. Proc Natl Acad Sci USA1995; 92(20): 9363-9367
CrossRef ADS Pubmed Google scholar
[3]
ChangBD, BroudeEV, DokmanovicM, ZhuH, RuthA, XuanY, KandelES, LauschE, ChristovK, RoninsonIB. A senescence-like phenotype distinguishes tumor cells that undergo terminal proliferation arrest after exposure to anticancer agents. Cancer Res1999; 59(15): 3761-3767
Pubmed
[4]
te PoeleRH, OkorokovAL, JardineL, CummingsJ, JoelSP. DNA damage is able to induce senescence in tumor cells in vitro and in vivo. Cancer Res2002; 62(6): 1876-1883
Pubmed
[5]
FangK, ChiuCC, LiCH, ChangYT, HwangHT. Cisplatin-induced senescence and growth inhibition in human non-small cell lung cancer cells with ectopic transfer of p16INK4a. Oncol Res2007; 16(10): 479-488
CrossRef ADS Pubmed Google scholar
[6]
WangX, WongSC, PanJ, TsaoSW, FungKH, KwongDL, ShamJS, NichollsJM. Evidence of cisplatin-induced senescent-like growth arrest in nasopharyngeal carcinoma cells. Cancer Res1998; 58(22): 5019-5022
Pubmed
[7]
PanieriE, GogvadzeV, NorbergE, VenkateshR, OrreniusS, ZhivotovskyB. Reactive oxygen species generated in different compartments induce cell death, survival, or senescence. Free Radic Biol Med2013; 57: 176-187
CrossRef ADS Pubmed Google scholar
[8]
LiSK, SmithDK, LeungWY, CheungAM, LamEW, DimriGP, YaoKM. FoxM1c counteracts oxidative stress-induced senescence and stimulates Bmi-1 expression. J Biol Chem2008; 283(24): 16545-16553
CrossRef ADS Pubmed Google scholar
[9]
QuK, XuX, LiuC, WuQ, WeiJ, MengF, ZhouL, WangZ, LeiL, LiuP. Negative regulation of transcription factor FoxM1 by p53 enhances oxaliplatin-induced senescence in hepatocellular carcinoma. Cancer Lett2013; 331(1): 105-114
CrossRef ADS Pubmed Google scholar
[10]
RobersonRS, KussickSJ, VallieresE, ChenSY, WuDY. Escape from therapy-induced accelerated cellular senescence in p53-null lung cancer cells and in human lung cancers. Cancer Res2005; 65(7): 2795-2803
CrossRef ADS Pubmed Google scholar
[11]
ColavittiR, FinkelT. Reactive oxygen species as mediators of cellular senescence. IUBMB Life2005; 57(4-5): 277-281
CrossRef ADS Pubmed Google scholar
[12]
IshikawaF. Cellular senescence, an unpopular yet trustworthy tumor suppressor mechanism. Cancer Sci2003; 94(11): 944-947
CrossRef ADS Pubmed Google scholar
[13]
ColladoM, GilJ, EfeyanA, GuerraC, SchuhmacherAJ, BarradasM, BenguríaA, ZaballosA, FloresJM, BarbacidM, BeachD, SerranoM. Tumour biology: senescence in premalignant tumours. Nature2005; 436(7051): 642
CrossRef ADS Pubmed Google scholar
[14]
ColladoM, SerranoM. Senescence in tumours: evidence from mice and humans. Nat Rev Cancer2010; 10(1): 51-57
CrossRef ADS Pubmed Google scholar
[15]
XueW, ZenderL, MiethingC, DickinsRA, HernandoE, KrizhanovskyV, Cordon-CardoC, LoweSW. Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas. Nature2007; 445(7128): 656-660
CrossRef ADS Pubmed Google scholar
[16]
JonesKR, ElmoreLW, Jackson-CookC, DemastersG, PovirkLF, HoltSE, GewirtzDA. p53-Dependent accelerated senescence induced by ionizing radiation in breast tumour cells. Int J Radiat Biol2005; 81(6): 445-458
CrossRef ADS Pubmed Google scholar
[17]
SantarosaM, Del ColL, ToninE, CaragnanoA, VielA, MaestroR. Premature senescence is a major response to DNA cross-linking agents in BRCA1-defective cells: implication for tailored treatments of BRCA1 mutation carriers. Mol Cancer Ther2009; 8(4): 844-854
CrossRef ADS Pubmed Google scholar
[18]
OzturkN, ErdalE, MumcuogluM, AkcaliKC, YalcinO, SenturkS, Arslan-ErgulA, GurB, YulugI, Cetin-AtalayR, YakicierC, YagciT, TezM, OzturkM. Reprogramming of replicative senescence in hepatocellular carcinoma-derived cells. Proc Natl Acad Sci USA2006; 103(7): 2178-2183
CrossRef ADS Pubmed Google scholar
[19]
PetrosWP, BroadwaterG, BerryD, JonesRB, VredenburghJJ, GilbertCJ, GibbsJP, ColvinOM, PetersWP. Association of high-dose cyclophosphamide, cisplatin, and carmustine pharmacokinetics with survival, toxicity, and dosing weight in patients with primary breast cancer. Clin Cancer Res2002; 8(3): 698-705
Pubmed
[20]
SchmittCA, FridmanJS, YangM, LeeS, BaranovE, HoffmanRM, LoweSW. A senescence program controlled by p53 and p16INK4a contributes to the outcome of cancer therapy. Cell2002; 109(3): 335-346
CrossRef ADS Pubmed Google scholar
[21]
ChangBD, XuanY, BroudeEV, ZhuH, SchottB, FangJ, RoninsonIB. Role of p53 and p21waf1/cip1 in senescence-like terminal proliferation arrest induced in human tumor cells by chemotherapeutic drugs. Oncogene1999; 18(34): 4808-4818
CrossRef ADS Pubmed Google scholar
[22]
ChenZ, TrotmanLC, ShafferD, LinHK, DotanZA, NikiM, KoutcherJA, ScherHI, LudwigT, GeraldW, Cordon-CardoC, PandolfiPP. Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis. Nature2005; 436(7051): 725-730
CrossRef ADS Pubmed Google scholar
[23]
RayessH, WangMB, SrivatsanES. Cellular senescence and tumor suppressor gene p16. Int J Cancer2012; 130(8): 1715-1725
CrossRef ADS Pubmed Google scholar
[24]
SteinGH, DrullingerLF, SoulardA, DulićV. Differential roles for cyclin-dependent kinase inhibitors p21 and p16 in the mechanisms of senescence and differentiation in human fibroblasts. Mol Cell Biol1999; 19(3): 2109-2117
Pubmed
[25]
VigneronA, VousdenKH. p53, ROS and senescence in the control of aging. Aging (Albany NY)2010; 2(8): 471-474
Pubmed
[26]
LimSC, ChoiJE, KangHS, HanSI. Ursodeoxycholic acid switches oxaliplatin-induced necrosis to apoptosis by inhibiting reactive oxygen species production and activating p53-caspase 8 pathway in HepG2 hepatocellular carcinoma. Int J Cancer2010; 126(7): 1582-1595
Pubmed

Acknowledgements

This study was supported by the National Natural Science Foundation of China (Grant Nos. 81201549 and 81272644).
Compliance with ethics guidelines
Kai Qu, Ting Lin, Zhixin Wang, Sinan Liu, Hulin Chang, Xinsen Xu, Fandi Meng, Lei Zhou, Jichao Wei, Minghui Tai, Yafeng Dong, and Chang liu declare that they have no conflict of interest. This manuscript does not involve a research protocol requiring approval from relevant institutional review board or ethics committee.

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2014 Higher Education Press and Springer-Verlag Berlin Heidelberg
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