z-logo
open-access-imgOpen Access
A Regulation Loop between YAP and NR4A1 Balances Cell Proliferation and Apoptosis
Author(s) -
Lingli He,
Liang Yuan,
Wentao Yu,
Yang Sun,
Dan Jiang,
Xiaodong Wang,
Xue Feng,
Zuoyun Wang,
Jinjin Xu,
Ruizeng Yang,
Wenxiang Zhang,
Hua Feng,
Hang-zi Chen,
Yi Arial Zeng,
Lijian Hui,
Qiao Wu,
Yonglong Zhang,
Lei Zhang
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2020.108284
Subject(s) - hippo signaling pathway , microbiology and biotechnology , cell growth , biology , carcinogenesis , apoptosis , signal transduction , regeneration (biology) , transcription factor , cell , phosphorylation , cancer research , cancer , genetics , gene
The Hippo signaling pathway maintains organ size and tissue homeostasis via orchestration of cell proliferation and apoptosis. How this pathway triggers cell apoptosis remains largely unexplored. Here, we identify NR4A1 as a target of the Hippo pathway that mediates the pro-apoptotic and anti-tumor effects of the Hippo pathway whereby YAP regulates the transcription, phosphorylation, and mitochondrial localization of NR4A1. NR4A1, in turn, functions as a feedback inhibitor of YAP to promote its degradation, thereby inhibiting the function of YAP during liver regeneration and tumorigenesis. Our studies elucidate a regulatory loop between NR4A1 and YAP to coordinate Hippo signaling activity during liver regeneration and tumorigenesis and highlight NR4A1 as a marker of Hippo signaling, as well as a therapeutic target for hepatocellular carcinoma.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom