激酶
信号转导
ASK1
生物
c-jun公司
机制(生物学)
细胞生物学
背景(考古学)
癌症研究
慢性肝病
蛋白激酶A
丝裂原活化蛋白激酶激酶
医学
转录因子
内科学
遗传学
基因
认识论
哲学
古生物学
肝硬化
作者
Sanda Win,Tin Aung Than,Jun Zhang,Christina Oo,Robert Win Maw Min,Neil Kaplowitz
出处
期刊:Hepatology
[Wiley]
日期:2018-04-06
卷期号:67 (5): 2013-2024
被引量:118
摘要
The c‐Jun‐N‐terminal‐kinase (JNK) family is highly conserved across species such as Drosophila, C. elegans , zebrafish and mammals, and plays a central role in hepatic physiologic and pathophysiologic responses. These responses range from cell death to cell proliferation and carcinogenesis, as well as metabolism and survival, depending on the specific context and duration of activation of the JNK signaling pathway. Recently, several investigators identified the key molecules in the JNK activation loop which include apoptosis signal‐regulating kinase (ASK1) and SH3‐domain binding protein 5 (Sab) and their involvement in acute or chronic liver disease models. Thus, regulating JNK activation through modulating the JNK activation loop may represent an important new strategy in the prevention and treatment of acute and chronic liver diseases. In this review, we will discuss the molecular pathophysiology of the JNK activation loop and its role in the pathogenesis of liver diseases. (H epatology 2018;67:2013‐2024).
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