摘要
索拉非尼是目前公认的治疗晚期原发性肝细胞癌的分子靶向药物,但原发性肝细胞癌对其耐药性的出现,影响了药物对肝癌的疗效。原发性肝细胞癌对索拉非尼耐药存在多种机制。肝癌细胞本身表皮生长因子受体的表达上调及其下游信号通路的异常改变,沉默信息调节因子1的过表达,肝癌细胞的自噬能力增强及间充质转变均可能导致其对索拉非尼耐药。肝癌血管内皮细胞出现耐药,肿瘤微环境中缺氧诱导因子-1α、趋化因子及其受体上调等也可能影响肿瘤对索拉非尼的敏感性。该文就原发性肝细胞癌对索拉非尼耐药机制的研究进展进行综述。
Sorafenib is the currently accepted first-line drug used for the treatment of advanced hepatocellular carcinoma, while re- sistance to sorafenib affects its curative effect. Available studies elucidated multiple mechanisms responsible for the resistance to sorafenib. The up-regulation of EGFR, dysregulation of signal pathways downstream of EGFR, and overexpression of silent in- formation regulator 1 in hepatoma ceils as well as epithelial-to- mesenchymal transition and increased autophage ability of hepa- toma ceils may increase the resistance to sorafenib. Resistance intumor endothelial cells and the upregulation of hypoxia-induced factor-1α, chemokine and its receptors in the tumor microenvi- romnent may also affect the sensitivity of hepatcellular carcinoma to sorafenib. This review provides an overview of the underlying mechanisms related to resistance to sorafenib of hepatocellular carcinoma.
出处
《中国药理学通报》
CAS
CSCD
北大核心
2013年第6期752-755,共4页
Chinese Pharmacological Bulletin
基金
国家卫生部"十二五"课题(No W2011BX043)
关键词
原发性肝细胞癌
索拉非尼
耐药
表皮生长因子受体
自噬
上皮细胞间充质转变
肿瘤血管内皮细胞
肿瘤微环境
hepatocellular carcinoma
sorafenib
drug resistance
epidermal growth factor receptor
autophage
epithclial-to-mesen- chymal transition
tumor endothelial cell
tumor microenvironment
