Transarterial chemoembolization aggravated peritumoral fibrosis via hypoxia‐inducible factor‐1α dependent pathway in hepatocellular carcinoma

医学 肝硬化 肝细胞癌 缺氧(环境) 纤维化 肝纤维化 病理 免疫组织化学 缺氧诱导因子 白蛋白 肝星状细胞 血管内皮生长因子 肿瘤缺氧 内科学 癌症研究 生物 化学 放射治疗 生物化学 有机化学 氧气 血管内皮生长因子受体 基因
作者
Kai Qu,Zhaoyong Yan,Yousheng Wu,Yibing Chen,Ping Qü,Xinsen Xu,Peng Yuan,Xiao‐Jun Huang,Jinliang Xing,Hongxin Zhang,Chang Liu,Jing Zhang
出处
期刊:Journal of Gastroenterology and Hepatology [Wiley]
卷期号:30 (5): 925-932 被引量:41
标识
DOI:10.1111/jgh.12873
摘要

Abstract Background and Aim It was commonly accepted that chemotherapeutic cytotoxicity was the main cause for hepatic failure in hepatocellular carcinoma patients after repeated transarterial chemoembolization ( TACE ). However, the effect of embolization‐induced hypoxia on liver cirrhosis has rarely been concerned. Methods Serum levels of alanine aminotransferase, aspartate aminotransferase, and albumin were used to detect liver injury. Hepatic artery ligation was performed in carbon tetrachloride‐induced rat hepatic fibrosis model to mimic the effect of hepatic hypoxia on liver fibrosis after TACE . S irius R ed staining and immunohistochemical analysis of alpha‐smooth muscle actin (α‐ SMA ) were used to detect the activation of hepatic stellate cells. Moreover, the expression of hypoxia and fibrosis‐related molecules were analyzed at protein and/or mRNA level. Results Patients showed a significant increase in alanine aminotransferase and aspartate aminotransferase ( P = 0.006), accompanied by a decrease in albumin ( P = 0.005) after repeated TACE . Hepatic artery ligation significantly promoted carbon tetrachloride‐induced rat liver fibrosis progression as indicated by S irius R ed and α‐ SMA staining, as well as increased expression of hypoxia‐inducible factor ( HIF )‐1α, transforming growth factor (TGF)‐β1, and vascular endothelial growth factor (VEGF). Conditioned media of hypoxia‐treated L 02 cells induced the expression of C ollagen I and α‐ SMA in LX ‐2 cells, which was inhibited by HIF ‐1α small interfering RNA . Finally, HIF ‐1α inhibitor LW 6 attenuated the hypoxia‐induced fibrosis progression in vivo . Conclusion Our data demonstrate that TACE ‐induced hepatic hypoxia aggravates the fibrosis progression in peritumoral liver tissue, thus leads to the deterioration of liver function. Intervention of HIF ‐1α might be a valuable strategy to optimize the efficacy and reduce the complication of TACE .
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