How Oncogenic Viruses Exploit p62-Mediated Selective Autophagy for Cancer Development.

Shunbin Ning, Ling Wang
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Abstract

The 2016 Nobel Prize in Physiology or Medicine was awarded to Dr. Yoshinori Ohsumi for his discoveries of mechanisms for autophagy. Autophagy is a fundamental and conserved cellular program essential for maintaining cellular homeostasis. Unlike non-selective autophagy (including mitophagy) that sorts harmful or surplus cellular contents to the lysosomes for degradation and recycling, selective autophagy is mediated by an increasing pool of receptors, such as p62, NBR1, TAX1BP1, NDP52, OPTN, BCL2L13, FUNDC1, CCDC50, TRIMs, and TOLLIP, and is generally invoked by certain stresses to specifically target functional substrates for lysosomal degradation to modulate various cellular responses [14].
致瘤病毒如何利用p62介导的选择性自噬促进癌症发展。
2016年诺贝尔生理学或医学奖授予大隅良典博士,以表彰他对自噬机制的发现。自噬是维持细胞稳态所必需的基本和保守的细胞程序。与非选择性自噬(包括有丝自噬)不同,选择性自噬将有害或多余的细胞内容物分类到溶酶体中进行降解和再循环,选择性自噬由越来越多的受体介导,如p62、NBR1、TAX1BP1、NDP52、OPTN、BCL2L13、FUNDC1、CCDC50、TRIMs和TOLLIP,并且通常在某些应激作用下特异性靶向溶酶体降解的功能底物来调节各种细胞反应[14]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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