Chinese agarwood petroleum ether extract suppressed gastric cancer progression via up-regulation of DNA damage-induced G0/G1 phase arrest and HO-1-mediated ferroptosis

Lishan Ouyang , Xuejiao Wei , Fei Wang , Huiming Huang , Xinyu Qiu , Zhuguo Wang , Peng Tan , Yufeng Gao , Ruoxin Zhang , Jun Li , Zhongdong Hu

Chinese Journal of Natural Medicines ›› 2025, Vol. 23 ›› Issue (10) : 1210 -1220.

PDF (5933KB)
Chinese Journal of Natural Medicines ›› 2025, Vol. 23 ›› Issue (10) :1210 -1220. DOI: 10.1016/S1875-5364(25)60876-4
Original article
research-article

Chinese agarwood petroleum ether extract suppressed gastric cancer progression via up-regulation of DNA damage-induced G0/G1 phase arrest and HO-1-mediated ferroptosis

Author information +
History +
PDF (5933KB)

Abstract

Gastric cancer (GC) is characterized by high morbidity and mortality rates. Chinese agarwood comprises the resin-containing wood of Aquilaria sinensis (Lour.) Gilg., traditionally utilized for treating asthma, cardiac ischemia, and tumors. However, comprehensive research regarding its anti-GC effects and underlying mechanisms remains limited. In this study, Chinese agarwood petroleum ether extract (CAPEE) demonstrated potent cytotoxicity against human GC cells, with half maximal inhibitory concentration (IC50) values for AGS, HGC27, and MGC803 cells of 2.89, 2.46, and 2.37 μg·mL−1, respectively, at 48 h. CAPEE significantly induced apoptosis in these GC cells, with B-cell lymphoma-2 (BCL-2) associated X protein (BAX)/BCL-2 antagonist killer 1 (BAK) likely mediating CAPEE-induced apoptosis. Furthermore, CAPEE induced G0/G1 phase cell cycle arrest in human GC cells via activation of the deoxyribonucleic acid (DNA) damage-p21-cyclin D1/cyclin-dependent kinase 4 (CDK4) signaling axis, and increased Fe2+, lipid peroxides and reactive oxygen species (ROS) levels, thereby inducing ferroptosis. Ribonucleic acid (RNA) sequencing, real-time quantitative polymerase chain reaction (RT-qPCR), and Western blotting analyses revealed CAPEE-mediated upregulation of heme oxygenase-1 (HO-1) in human GC cells. RNA interference studies demonstrated that HO-1 knockdown reduced CAPEE sensitivity and inhibited CAPEE-induced ferroptosis in human GC cells. Additionally, CAPEE administration exhibited robust in vivo anti-GC activity without significant toxicity in nude mice while inhibiting tumor cell growth and promoting apoptosis in tumor tissues. These findings indicate that CAPEE suppresses human GC cell growth through upregulation of the DNA damage-p21-cyclin D1/CDK4 signaling axis and HO-1-mediated ferroptosis, suggesting its potential as a candidate drug for GC treatment.

Keywords

Chinese agarwood petroleum ether extract (CAPEE) / Gastric cancer / G0/G1 phase arrest / Ferroptosis / DNA damage-p21-Cyclin D1/CDK4 signaling axis / HO-1

Cite this article

Download citation ▾
Lishan Ouyang, Xuejiao Wei, Fei Wang, Huiming Huang, Xinyu Qiu, Zhuguo Wang, Peng Tan, Yufeng Gao, Ruoxin Zhang, Jun Li, Zhongdong Hu. Chinese agarwood petroleum ether extract suppressed gastric cancer progression via up-regulation of DNA damage-induced G0/G1 phase arrest and HO-1-mediated ferroptosis. Chinese Journal of Natural Medicines, 2025, 23(10): 1210-1220 DOI:10.1016/S1875-5364(25)60876-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Sung H, Ferlay J, Siegel RL, et al.Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin.2021; 71(3):209-249. https://doi.org/10.3322/caac.21660.

[2]

Li K, Zhang A, Li X, et al. Advances in clinical immunotherapy for gastric cancer. Biochim Biophys Acta Rev Cancer. 2021; 1876(2): 188615. https://doi.org/10.1016/j.bbcan.2021.188615.

[3]

Wang S, Wang C, Peng D, et al. Agarwood essential oil displays sedative-hypnotic effects through the GABAergic system. Molecules. 2017; 22(12):2190. https://doi.org/10.3390/molecules22122190.

[4]

Li W, Chen HQ, Wang H, et al. Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesis. Nat Prod Rep. 2021; 38(3):528-565. https://doi.org/10.1039/d0np00042f.

[5]

Hashim YZ, Kerr PG, Abbas P, et al. Aquilaria spp. (agarwood) as source of health beneficial compounds: a review of traditional use, phytochemistry and pharmacology. J Ethnopharmacol. 2016; 189:331-360. https://doi.org/10.1016/j.jep.2016.06.055.

[6]

Shivanand P, Arbie NF, Krishnamoorthy S, et al. Agarwood-the fragrant molecules of a wounded tree. Molecules. 2022; 27(11):3386. https://doi.org/10.3390/molecules27113386.

[7]

Hashim YZ, Phirdaous A, Azura A. Screening of anticancer activity from agarwood essential oil. Pharmacognosy Res. 2014; 6(3):191-194. https://doi.org/10.4103/0974-8490.132593.

[8]

Dahham SS, Hassan LE, Ahamed MB, et al. In vivo toxicity and antitumor activity of essential oils extract from agarwood (Aquilaria crassna). BMC Complement Altern Med. 2016;16:236. https://doi.org/10.1186/s12906-016-1210-1.

[9]

Zhang H, Ma JL, Chang C, et al.Gastroprotective 2-(2-phenylethyl)chromone-sesquiterpene hybrids from the resinous wood of Aquilaria sinensis (Lour.) Gilg. Bioorg Chem. 2023;133:106396. https://doi.org/10.1016/j.bioorg.2023.106396.

[10]

Huo HX, Zhu ZX, Pang DR, et al.Anti-neuroinflammatory sesquiterpenes from Chinese eaglewood. Fitoterapia. 2015; 106:115-121. https://doi.org/10.1016/j.fitote.2015.08.009.

[11]

Chen X, Zhao Y, Yang A, et al.Chinese Dragon’s Blood EtOAc extract inhibits liver cancer growth through downregulation of Smad3. Front Pharmacol. 2020;11:669. https://doi.org/10.3389/fphar.2020.00669.

[12]

Hu Z, Wang Y, Huang F, et al. Brain-expressed X-linked 2 is pivotal for hyperactive mechanistic target of rapamycin (mTOR)-mediated tumorigenesis. J Biol Chem. 2015; 290(42):25756-25765. https://doi.org/10.1074/jbc.M115.665208.

[13]

Jin F, Jiang K, Ji S, et al. Deficient TSC1/TSC2-complex suppression of SOX9-osteopontin-AKT signalling cascade constrains tumour growth in tuberous sclerosis complex. Hum Mol Genet. 2017; 26(2):407-419. https://doi.org/10.1093/hmg/ddw397.

[14]

He M, Zhang G, Shen F, et al. Effects of Z-VaD-Ala-Asp-fluoromethyl ketone (Z-VAD-FMK) and acetyl-Asp-Glu-Val-Asp-aldehyde (Ac-DEVD-CHO) on inflammation and mucus secretion in mice exposed to cigarette smoke. Int J Chron Obstruct Pulmon Dis. 2023; 18:69-78. https://doi.org/10.2147/copd.S385748.

[15]

McArthur K, Whitehead LW, Heddleston JM, et al. BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis. Science. 2018;359:6378. https://doi.org/10.1126/science.aao6047.

[16]

Hershko C, Weatherall DJ. Iron-chelating therapy. Crit Rev Clin Lab Sci. 1988; 26(4):303-345. https://doi.org/10.3109/10408368809105894.

[17]

Pedre B, Barayeu U, Ezeriņa D, et al. The mechanism of action of N-acetylcysteine (NAC): the emerging role of H2S and sulfane sulfur species. Pharmacol Ther. 2021;228:107916. https://doi.org/10.1016/j.pharmthera.2021.107916.

[18]

Miotto G, Rossetto M, Di Paolo ML, et al.Insight into the mechanism of ferroptosis inhibition by ferrostatin-1. Redox Biol. 2020;28:101328. https://doi.org/10.1016/j.redox.2019.101328.

[19]

Wang X, Gao B, Liu X, et al. Salinity stress induces the production of 2-(2-phenylethyl)chromones and regulates novel classes of responsive genes involved in signal transduction in Aquilaria sinensis calli. BMC Plant Biol. 2016; 16(1):119. https://doi.org/10.1186/s12870-016-0803-7.

[20]

Zhang X, Wang LX, Hao R, et al. Sesquiterpenoids in agarwood: biosynthesis, microbial induction, and pharmacological activities. J Agric Food Chem. 2024; 72(42):23039-23052. https://doi.org/10.1021/acs.jafc.4c06383.

[21]

Wang S, Wang C, Yu Z, et al. Agarwood essential oil ameliorates restrain stress-induced anxiety and depression by inhibiting HPA axis hyperactivity. Int J Mol Sci. 2018; 19(11):3468. https://doi.org/10.3390/ijms19113468.

[22]

Wang Y, Hussain M, Jiang Z, et al. Aquilaria species (Thymelaeaceae) distribution, volatile and non-volatile phytochemicals, pharmacological uses, agarwood grading system, and induction methods. Molecules. 2021; 26(24):7708. https://doi.org/10.3390/molecules26247708.

[23]

Xie Y, Song L, Li C, et al. Eudesmane-type and agarospirane-type sesquiterpenes from agarwood of Aquilaria agallocha. Phytochemistry. 2021;192:112920. https://doi.org/10.1016/j.phytochem.2021.112920.

[24]

Ye W, He X, Wu H, et al. Identification and characterization of a novel sesquiterpene synthase from Aquilaria sinensis: an important gene for agarwood formation. Int J Biol Macromol. 2018; 108:884-892. https://doi.org/10.1016/j.ijbiomac.2017.10.183.

[25]

Wang S, Yu Z, Wang C, et al. Chemical constituents and pharmacological activity of agarwood and Aquilaria plants. Molecules. 2018; 23(2):342. https://doi.org/10.3390/molecules23020342.

[26]

Dahham SS, Tabana YM, Iqbal MA, et al. The anticancer, antioxidant and antimicrobial properties of the sesquiterpene β-caryophyllene from the essential oil of Aquilaria crassna. Molecules. 2015; 20(7):11808-11829. https://doi.org/10.3390/molecules200711808.

[27]

Huang XL, Cai D, Gao P, et al. Aquilariperoxide A, a sesquiterpene dimer from agarwood of Aquilaria sinensis with dual antitumor and antimalarial rffects. J Org Chem. 2023; 88(13):8352-8359. https://doi.org/10.1021/acs.joc.3c00372.

[28]

Morana O, Wood W, Gregory CD.The apoptosis paradox in cancer. Int J Mol Sci. 2022; 23(3):1328. https://doi.org/10.3390/ijms23031328.

[29]

Pistritto G, Trisciuoglio D, Ceci C, et al. Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies. Aging (Albany NY). 2016; 8(4):603-619. https://doi.org/10.18632/aging.100934.

[30]

Kayagaki N, Webster JD, Newton K. Control of cell death in health and disease. Annu Rev Pathol. 2024; 19:157-180. https://doi.org/10.1146/annurev-pathmechdis-051022-014433.

[31]

Hidalgo M, Rowinsky EK. The rapamycin-sensitive signal transduction pathway as a target for cancer therapy. Oncogene. 2000; 19(56):6680-6686. https://doi.org/10.1038/sj.onc.1204091.

[32]

Liu J, Guo Y, Cao J.Matrine triggers colon cancer cell apoptosis and G0/G1 cell cycle arrest via mediation of microRNA-22. Phytother Res. 2020; 34(7):1619-1628. https://doi.org/10.1002/ptr.6626.

[33]

Khan F, Pandey P, Upadhyay TK, et al. Anti-cancerous effect of rutin against HPV-C33A cervical cancer cells via G0/G1 cell cycle arrest and apoptotic induction. Endocr Metab Immune Disord Drug Targets. 2020; 20(3):409-418. https://doi.org/10.2174/1871530319666190806122257.

[34]

Chen J, Amos CI, Merriman KW, et al. Genetic variants of p21 and p27 and pancreatic cancer risk in non-Hispanic Whites: a case-control study. Pancreas. 2010; 39(1):1-4. https://doi.org/10.1097/MPA.0b013e3181bd51c8.

[35]

Goel S, DeCristo MJ, McAllister SS, et al. CDK4/6 Inhibition in cancer: beyond cell cycle arrest. Trends Cell Biol. 2018; 28(11):911-925. https://doi.org/10.1016/j.tcb.2018.07.002.

[36]

Shamloo B, Usluer S. p21 in cancer research. Cancers (Basel). 2019; 11(8):1178. https://doi.org/10.3390/cancers11081178.

[37]

Usugi E, Ishii K, Hirokawa Y, et al. Antifibrotic agent pirfenidone suppresses proliferation of human pancreatic cancer cells by inducing G0/G1 cell cycle arrest. Pharmacology. 2019; 103(5-6):250-256. https://doi.org/10.1159/000496831.

[38]

Ricciuti B, Recondo G, Spurr LF, et al. Impact of DNA damage response and repair (DDR) gene mutations on efficacy of PD-L1 immune checkpoint inhibition in non-small cell lung cancer. Clin Cancer Res. 2020; 26(15):4135-4142. https://doi.org/10.1158/1078-0432.Ccr-19-3529.

[39]

Brown JS, O'Carrigan B, Jackson SP, et al. Targeting DNA repair in cancer: beyond PARP inhibitors. Cancer Discov. 2017; 7(1):20-37. https://doi.org/10.1158/2159-8290.Cd-16-0860.

[40]

Kozyrska K, Pilia G, Vishwakarma M, et al. p53 directs leader cell behavior, migration, and clearance during epithelial repair. Science. 2022; 375(6581):eabl8876. https://doi.org/10.1126/science.abl8876.

[41]

Tian Y, Wang L, Chen X, et al.DHMMF, a natural flavonoid from Resina Draconis, inhibits hepatocellular carcinoma progression via inducing apoptosis and G2/M phase arrest mediated by DNA damage-driven upregulation of p21. Biochem Pharmacol. 2023;211:115518. https://doi.org/10.1016/j.bcp.2023.115518.

[42]

Wang D, Tang L, Zhang Y, et al. Regulatory pathways and drugs associated with ferroptosis in tumors. Cell Death Dis. 2022; 13(6):544. https://doi.org/10.1038/s41419-022-04927-1.

[43]

Dolma S, Lessnick SL, Hahn WC, et al. Identification of genotype-selective antitumor agents using synthetic lethal chemical screening in engineered human tumor cells. Cancer Cell. 2003; 3(3):285-296. https://doi.org/10.1016/s1535-6108(03)00050-3.

[44]

Chiang SK, Chen SE, Chang LC. A dual role of heme oxygenase-1 in cancer cells. Int J Mol Sci. 2018; 20(1):39. https://doi.org/10.3390/ijms20010039.

[45]

Tang Z, Ju Y, Dai X, et al. HO-1-mediated ferroptosis as a target for protection against retinal pigment epithelium degeneration. Redox Biol. 2021;43:101971. https://doi.org/10.1016/j.redox.2021.101971.

[46]

Ding L, Dang S, Sun M, et al. Quercetin induces ferroptosis in gastric cancer cells by targeting SLC1A5 and regulating the p-Camk2/p-DRP1 and NRF2/GPX4 axis. Free Radic Biol Med. 2024; 213:150-163. https://doi.org/10.1016/j.freeradbiomed.2024.01.002.

[47]

Lu C, Zhang Z, Fan Y, et al. Shikonin induces ferroptosis in osteosarcomas through the mitochondrial ROS-regulated HIF-1α/HO-1 axis. Phytomedicine. 2024;135:156139. https://doi.org/10.1016/j.phymed.2024.156139.

[48]

Chen P, Li X, Zhang R, et al. Combinative treatment of β-elemene and cetuximab is sensitive to KRAS mutant colorectal cancer cells by inducing ferroptosis and inhibiting epithelial-mesenchymal transformation. Theranostics. 2020; 10(11):5107-5119. https://doi.org/10.7150/thno.44705.

[49]

Wei R, Zhao Y, Wang J, et al. Tagitinin C induces ferroptosis through PERK-Nrf2-HO-1 signaling pathway in colorectal cancer cells. Int J Biol Sci. 2021; 17(11):2703-2717. https://doi.org/10.7150/ijbs.59404.

[50]

Xu Y, Tong Y, Lei Z, et al. Abietic acid induces ferroptosis via the activation of the HO-1 pathway in bladder cancer cells. Biomed Pharmacother. 2023;158:114154. https://doi.org/10.1016/j.biopha.2022.114154.

PDF (5933KB)

83

Accesses

0

Citation

Detail

Sections
Recommended

/