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STC2 as a novel mediator for Mus81-dependent proliferation and survival in hepatocellular carcinoma.

Authors :
Wu, Fan
Li, Ting-Yue
Su, Shu-Chao
Yu, Ji-Shang
Zhang, Hao-Lu
Tan, Guo-Qian
Liu, Jian-Wei
Wang, Bai-Lin
Source :
Cancer Letters. Mar2017, Vol. 388, p177-186. 10p.
Publication Year :
2017

Abstract

Methyl methansulfonate and UV sensitive gene clone 81 (Mus81) is a critical DNA repair gene that has been implicated in development of several cancers including hepatocellular carcinoma (HCC). However, whether Mus81 can affect proliferation and survival of HCC remains unknown. In the present study, we demonstrated that the knockdown of Mus81 was associated with suppressed proliferation and elevated apoptosis of HCC cells in vitro and in vivo. Multilayered screenings, including DNA microarray, high content screen, and real-time PCR validation, identified STC2 as a proliferation-facilitating gene significantly down-regulated in HCC cells upon Mus81 knockdown. STC2 expression was also closely correlated to Mus81 expression in HCC tissues. More importantly, the restoration of STC2 expression recovered the compromised cell proliferation and survival in Mus81 depleted HCC cells. Furthermore, Mus81 knockdown was associated with the activation of APAF1, APC, and PTEN pathways and concurrent inhibition of MAPK pathway through decreasing STC2 expression. In conclusion, Mus81 knockdown suppresses proliferation and survival of HCC cells likely by downregulating STC2 expression, implicating Mus81 as a therapeutic target for HCC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03043835
Volume :
388
Database :
Academic Search Index
Journal :
Cancer Letters
Publication Type :
Academic Journal
Accession number :
121356292
Full Text :
https://doi.org/10.1016/j.canlet.2016.11.039