4.7 Article

miR-346 functions as a pro-survival factor under ER stress by activating mitophagy

期刊

CANCER LETTERS
卷 413, 期 -, 页码 69-81

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2017.10.030

关键词

UPR; miR-346; ER stress; GSK3B; Autophagy

类别

资金

  1. National Natural Science Foundation of China [91029714, 31270818: 81572790]
  2. Natural Science Foundation of Tianjin [12JCZDJC25100]

向作者/读者索取更多资源

Stress in the endoplasmic reticulum (ER) triggers the unfolded protein response (UPR), which attempts to restore normal function of the ER. Both autophagy and miRNAs have been reported to participate in the process of ER stress, but the relationship between these two factors is still obscure. In this study, we demonstrated that miR-346, which was induced under ER stress, modulated autophagic flux in HeLa cells. By regulating the process of autophagy, miR-346 reduced the ROS level in the cells, thus protecting them from death following ER stress. Furthermore, we demonstrated that GSK3B was the target of miR-346 and participated in ER stress-related autophagy. miR-346 activated autophagy by interrupting the association between BCL2 and BECN1 in a GSK3B-dependent manner. Our findings shed new light on the role of miRNAs during ER stress and suggest a new mechanism for the induction of autophagy under ER stress. (c) 2017 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据