Targeting p38γ synergistically enhances sorafenib-induced cytotoxicity in hepatocellular carcinoma

被引:0
作者
Huang, Chen [1 ,2 ,3 ]
Zhang, Chenliang [1 ,2 ,3 ]
Li, Jiajin [4 ]
Duan, Yichun [3 ]
Tang, Qiulin [1 ,2 ]
Bi, Feng [1 ,2 ,3 ]
机构
[1] Sichuan Univ, Div Abdominal Tumor Multimodal Treatment, Ctr Canc, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Lab Mol Targeted Therapy Oncol, West China Hosp, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Div Abdominal Tumor Multimodal Treatment, Ctr Canc, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; Sorafenib; P38; gamma; Autophagy; Cell drug resistance; CANCER CELLS; PIRFENIDONE; AUTOPHAGY; PROLIFERATION; PROGRESSION; CATENIN; GROWTH;
D O I
10.1007/s10565-024-09979-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sorafenib (Sora) is a first-line treatment for patients with advanced hepatocellular carcinoma (HCC). It can significantly improve the survival rate of patients with advanced HCC, but it is prone to drug resistance during treatment, so the therapeutic effect is extremely limited. Here, we demonstrate that an elevated expression of protein kinase p38 gamma in hepatocellular carcinoma cells diminishes the tumor cells' sensitivity to Sora. Pirfenidone (PFD) can augment Sora's inhibitory effect on hepatocellular carcinoma by specifically targeting p38 gamma. Our study further uncovers that pirfenidone can synergistically boost the anti-hepatocellular carcinoma impact of Sora by impeding the autophagy heightened by p38 gamma. Taken together, our findings suggest that pirfenidone can work in concert with Sora to intensify its anti-tumor effect on hepatocellular carcinoma, thereby offering a novel therapeutic approach for Sora-mediated tumor treatment.
引用
收藏
页数:18
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