Treatise:Mechanism Exploration

Regorafenib synergy with irinotecan targets the proliferation, apoptosis and migration of hepatocellular carcinoma cells under hypoxia

  • Shuo HE ,
  • Jun ZHANG
Expand
  • 1.Department of Pathology,Guizhou Medical University,Guiyang 550004,Guizhou,China
    2.Department of Pathology,Affiliated Hospital of Guizhou Medical University,Guiyang 550004,Guizhou,China

Received date: 2025-11-05

  Online published: 2026-04-28

Abstract

Objective This study investigates the mechanism of combination therapy of Regorafenib and Irinotecan in hepatocellular carcinoma under hypoxic conditions and aims to provide a new therapeutic strategy for anticancer drugs combination to improve outcomes. Methods The median inhibitory concentration (IC50) of drugs against hepatocellular carcinoma cells under normoxic and hypoxic conditions were determined, dose-response curves were plotted to evaluate the sensitivity to Oxaliplatin Regorafenib and Irinotecan. Combined effects of different concentrations of Regorafenib and Irinotecan on hepatocellular carcinoma cells were analyzed using CompuSyn and SynergyFinder 3.0 software. The impacts on cell death rates were determined via flow cytometry. The effects on cell proliferation were determined using EdU proliferation assays. The influences on cell migration were assessed through Transwell and wound healing assays. The alterations of relevant proteins in signaling pathways were detected by Western blot experiments. Results Hypoxia had no significant effect on the IC50 values of Regorafenib and Irinotecan. Compared to Oxaliplatin, both agents can overcome hypoxia-induced treatment tolerance. Under hypoxic conditions, Regorafenib and Irinotecan exhibited synergistic effects with a combination index (CI values) < 1 and a ZIP synergy score > 10. Compared to regorafenib and irinotecan groups, the combination of Regorafenib and Irinotecan significantly increased the cells proportion in SubG1 phase (P < 0.000 1) and exhibited combined inhibitory effects on cell migration (P < 0.000 1). Under hypoxic conditions, Irinotecan increased the proportion of proliferating cells (P < 0.000 1), which significantly decreased upon combination with Regorafenib (P < 0.000 1), accompanied by reduced intracellular CyclinD1 levels (P < 0.000 1) Under hypoxic conditions, Irinotecan upregulated HIF-1α expression and activated ERK1/2 signaling (P < 0.000 1), combination with Regorafenib modulated Irinotecan-mediated expression or activation (P < 0.000 1), and the combination therapy downregulated AKT and ERK1/2 signaling activity (P < 0.001). Conclusions Under hypoxic conditions, the combination of Regorafenib and Irinotecan overcomes hypoxia-induced treatment tolerance, promotes hepatocellular carcinoma cell death, and inhibits hepatocellular carcinoma cell proliferation and migration. This synergistic effect may be associated with the suppression of HIF-1α and CyclinD1 expression, as well as the downregulation of AKT and ERK1/2 phosphorylation levels in hepatocellular carcinoma cells.

Cite this article

Shuo HE , Jun ZHANG . Regorafenib synergy with irinotecan targets the proliferation, apoptosis and migration of hepatocellular carcinoma cells under hypoxia[J]. The Journal of Practical Medicine, 2026 , 42(8) : 1397 -1406 . DOI: 10.3969/j.issn.1006-5725.2026.08.013

References

[1] HAN B, ZHENG R, ZENG H, et al. Cancer incidence and mortality in China, 2022[J]. J Natl Cancer Cent, 2024, 4(1): 47-53. doi:10.1016/j.jncc.2024.01.006 .
[2] LI Y, ZHAO L, LI X F. Targeting hypoxia: Hypoxia-activated prodrugs in cancer therapy[J]. Front Oncol, 2021, 11: 700407. doi:10.3389/fonc.2021.700407 .
[3] CHEN Z, HAN F, DU Y, et al. Hypoxic microenvironment in cancer: Molecular mechanisms and therapeutic interventions[J]. Signal Transduct Target Ther, 2023, 8(1): 70. doi:10.1038/s41392-023-01332-8 .
[4] 中华人民共和国国家卫生健康委员会医政司. 原发性肝癌诊疗指南(2024年版)[J]. 协和医学杂志, 2024, 15(3): 532-558. doi:10.12290/xhyxzz.2024-0304 .
[5] HUANG W L, HSU Y C, LUO C W, et al. Targeting the CDK7-MDK axis to suppresses irinotecan resistance in colorectal cancer[J]. Life Sci, 2024, 353: 122914. doi:10.1016/j.lfs.2024.122914 .
[6] LLOVET J M, KELLEY R K, VILLANUEVA A, et al. Hepatocellular carcinoma[J]. Nat Rev Dis Primers, 2021, 7(1): 6. doi:10.1038/s41572-020-00240-3 .
[7] ADEBAYO A S, AGBAJE K, ADESINA S K, et al. Colorectal cancer: Disease process, current treatment options, and future perspectives[J]. Pharmaceutics, 2023, 15(11): 2620. doi:10.3390/pharmaceutics15112620 .
[8] FONDEVILA F, MéNDEZ-BLANCO C, FERNáNDEZ-PALANCA P, et al. Anti-tumoral activity of single and combined regorafenib treatments in preclinical models of liver and gastrointestinal cancers[J]. Exp Mol Med, 2019, 51(9): 1-15. doi:10.1038/s12276-019-0308-1 .
[9] ZHANG C, WU L W, LI Z D, et al. DYRK1A suppression attenuates HIF-1α accumulation and enhances the anti-liver cancer effects of regorafenib and sorafenib under hypoxic conditions[J]. Int J Oncol, 2022, 60(4): 45. doi:10.3892/ijo.2022.5335 .
[10] ZHANG J, ZHOU L, ZHAO S, et al. The CDK4/6 inhibitor palbociclib synergizes with irinotecan to promote colorectal cancer cell death under hypoxia[J]. Cell Cycle, 2017, 16(12): 1193-1200. doi:10.1080/15384101.2017.1320005 .
[11] IANEVSKI A, GIRI A K, AITTOKALLIO T. SynergyFinder 3.0: An interactive analysis and consensus interpretation of multi-drug synergies across multiple samples[J]. Nucleic Acids Res, 2022, 50(W1): W739-W743. doi:10.1093/nar/gkac382 .
[12] 杨伟, 梁念孩, 夏会东, 等. 微管蛋白2A在肝细胞癌中的表达及其在缺氧条件下对肝癌细胞恶性生物学行为的影响[J]. 实用医学杂志, 2025, 41(20): 3175-3184. doi:10.3969/j.issn.1006-5725.2025.20.005 .
[13] LADD A D, DUARTE S, SAHIN I, et al. Mechanisms of drug resistance in HCC[J]. Hepatology, 2024, 79(4): 926-940. doi:10.1097/HEP.0000000000000237 .
[14] CHEN Z X, MU M Y, YANG G, et al. Hypoxia-induced DTL promotes the proliferation, metastasis, and sorafenib resistance of hepatocellular carcinoma through ubiquitin-mediated degradation of SLTM and subsequent Notch pathway activation[J]. Cell Death Dis, 2024, 15(10): 734. doi:10.1038/s41419-024-07089-4 .
[15] LIANG C, DONG Z, CAI X, et al. Hypoxia induces sorafenib resistance mediated by autophagy via activating FOXO3a in hepatocellular carcinoma[J]. Cell Death Dis, 2020, 11(11): 1017. doi:10.1038/s41419-020-03233-y .
[16] 王毅, 何硕, 杨斯昀, 等. 5-氟尿嘧啶联合重组人细胞珠蛋白治疗缺氧诱导化疗耐受肝细胞癌的体外实验[J]. 实用医学杂志, 2024, 40(22): 3146-3154. doi:10.3969/j.issn.1006-5725.2024.22.005 .
[17] CHEN Z Y, LI J, ZHU S D, et al. Harmine reinforces the effects of regorafenib on suppressing cell proliferation and inducing apoptosis in liver cancer cells[J]. Exp Ther Med, 2022, 23(3): 209. doi:10.3892/etm.2022.11132 .
[18] YUAN T, WU R, WANG W, et al. Synergistic antitumor activity of regorafenib and rosuvastatin in colorectal cancer[J]. Front Pharmacol, 2023, 14: 1136114. doi:10.3389/fphar.2023.1136114 .
[19] JASSI C, KUO W W, CHANG Y C, et al. Aloin and CPT-11 combination activates miRNA-133b and downregulates IGF1R- PI3K/AKT/mTOR and MEK/ERK pathways to inhibit colorectal cancer progression[J]. Biomed Pharmacother, 2023, 169: 115911. doi:10.1016/j.biopha.2023.115911 .
[20] WU M M, ZHANG Z, TONG C W S, et al. Repurposing of niclosamide as a STAT3 inhibitor to enhance the anticancer effect of chemotherapeutic drugs in treating colorectal cancer[J]. Life Sci, 2020, 262: 118522. doi:10.1016/j.lfs.2020.118522 .
[21] YANG T, HUO J, XU R, et al. Synergistic effect of toosendanin and regorafenib against cell proliferation and migration by regulating WWOX signaling pathway in hepatocellular carcinoma[J]. Phytother Res, 2021, 35(8): 4567-4578. doi:10.1002/ptr.7174 .
[22] WU W, DONG J, GOU H, et al. EGCG synergizes the therapeutic effect of irinotecan through enhanced DNA damage in human colorectal cancer cells[J]. J Cell Mol Med, 2021, 25(16): 7913-7921. doi:10.1111/jcmm.16718 .
[23] 朱磊, 李政委, 盛利平, 等. HIF-1α/BNIP3介导的线粒体自噬对创伤性脑损伤后神经元凋亡的影响[J]. 中华神经医学杂志, 2023, 22(9): 865-874. doi:10.3760/cma.j.cn115354-20230712-00385 .
[24] MU M, ZHANG Q, LI J, et al. USP51 facilitates colorectal cancer stemness and chemoresistance by forming a positive feed-forward loop with HIF1A[J]. Cell Death Differ, 2023, 30(11): 2393-2407. doi:10.1038/s41418-023-01228-8 .
[25] SHIGETA K, HASEGAWA M, HISHIKI T, et al. IDH2 stabilizes HIF-1α-induced metabolic reprogramming and promotes chemoresistance in urothelial cancer[J]. EMBO J, 2023, 42(4): e110620. doi:10.15252/embj.2022110620 .
[26] MAMO M, YE I C, DIGIACOMO J W, et al. Hypoxia alters the response to anti-EGFR therapy by regulating EGFR expression and downstream signaling in a DNA methylation-specific and HIF-dependent manner[J]. Cancer Res, 2020, 80(22): 4998-5010. doi:10.1158/0008-5472.CAN-20-1232 .
[27] SHI Y, GILKES D M. HIF-1 and HIF-2 in cancer: Structure, regulation, and therapeutic prospects[J]. Cell Mol Life Sci, 2025, 82(1): 44. doi:10.1007/s00018-024-05537-0 .
[28] LI Q, LI Z, LUO T, et al. Targeting the PI3K/AKT/mTOR and RAF/MEK/ERK pathways for cancer therapy[J]. Mol Biomed, 2022, 3(1): 47. doi:10.1186/s43556-022-00110-2 .
Outlines

/