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去γ-羧基凝血酶原在肝细胞癌进展中的作用及信号通路

Roles and Signaling Pathways of Des-γ-Carboxyprothrombin in the Progression of Hepatocellular Carcinoma.

作者信息

Cui Shu-Xiang, Yu Xin-Feng, Qu Xian-Jun

机构信息

a Beijing Key Laboratory of Environmental Toxicology, School of Public Health , Capital Medical University , Beijing , China.

b Department of Pharmacology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.

出版信息

Cancer Invest. 2016 Oct 20;34(9):459-464. doi: 10.1080/07357907.2016.1227445. Epub 2016 Sep 27.

Abstract

Des-γ-carboxyprothrombin (DCP), an abnormal prothrombin produced in human hepatocellular carcinoma (HCC), plays crucial roles in the progression of HCC. DCP binding to cellular mesenchymal-epithelial transition factor (c-Met) is an initial event and consequently stimulates HCC through the increase of c-Met-Janus kinase 1- signal transducers and activators of transcription pathways. DCP stimulates HCC invasion through activation of matrix metalloproteinase via upregulation of extracellular signal-regulated kinase-mitogen-activated protein kinase (MAPK) pathway. DCP stimulates HCC angiogenesis through activation of the DCP-kinase insert domain receptor-phospholipaseC-γ-MAPK pathway. Identification of these pathways is important for designing the therapeutic strategy for HCC.

摘要

去γ-羧基凝血酶原(DCP)是人类肝细胞癌(HCC)中产生的一种异常凝血酶原,在HCC进展中起关键作用。DCP与细胞间充质-上皮转化因子(c-Met)结合是起始事件,进而通过增加c-Met-janus激酶1-信号转导和转录激活因子途径刺激HCC。DCP通过细胞外信号调节激酶-丝裂原活化蛋白激酶(MAPK)途径上调激活基质金属蛋白酶,从而刺激HCC侵袭。DCP通过激活DCP-激酶插入结构域受体-磷脂酶C-γ-MAPK途径刺激HCC血管生成。识别这些途径对于设计HCC的治疗策略很重要。

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