YAP inhibits autophagy and promotes progression of colorectal cancer via upregulating Bcl-2 expression

被引:83
|
作者
Jin, Lan [1 ,2 ]
Chen, Yunhe [1 ,2 ]
Cheng, Dan [1 ]
He, Zhikai [1 ]
Shi, Xinyi [3 ]
Du, Boyu [1 ]
Xi, Xueyan [1 ]
Gao, Yujing [3 ]
Guo, Yang [1 ,2 ]
机构
[1] Hubei Univ Med, Sch Basic Med Sci, Dept Immunol, Shiyan 442000, Hubei, Peoples R China
[2] Hubei Univ Med, Hubei Key Lab Embryon Stem Cell Res, Shiyan 442000, Hubei, Peoples R China
[3] Ningxia Med Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Key Lab Fertil Preservat & Maintenance,Minist Edu, Yinchuan, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
YES-ASSOCIATED PROTEIN; CELL-DEATH; HIPPO PATHWAY; PROLIFERATION; GROWTH; CHEMORESISTANCE; BIOLOGY;
D O I
10.1038/s41419-021-03722-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Colorectal cancer (CRC) is one of the most aggressive and lethal cancers. The role of autophagy in the pathobiology of CRC is intricate, with opposing functions manifested in different cellular contexts. The Yes-associated protein (YAP), a transcriptional coactivator inactivated by the Hippo tumor-suppressor pathway, functions as an oncoprotein in a variety of cancers. In this study, we found that YAP could negatively regulate autophagy in CRC cells, and consequently, promote tumor progression of CRC in vitro and in vivo. Mechanistically, YAP interacts with TEAD forming a complex to upregulate the transcription of the apoptosis-inhibitory protein Bcl-2, which may subsequently facilitate cell survival by suppressing autophagy-related cell death; silencing Bcl-2 expression could alleviate YAP-induced autophagy inhibition without affecting YAP expression. Collectively, our data provide evidence for YAP/Bcl-2 as a potential therapeutic target for drug exploration against CRC.
引用
收藏
页数:10
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