Induction of entosis by epithelial cadherin expression

被引:0
|
作者
Qiang Sun
Edmund S Cibas
Hongyan Huang
Louis Hodgson
Michael Overholtzer
机构
[1] Laboratory of Cell Engineering,Department of Pathology
[2] Institute of Biotechnology,Department of Oncology
[3] Cell Biology Program,Department of Anatomy and Structural Biology and Gruss
[4] Memorial Sloan-Kettering Cancer Center,Lipper Biophotonics Center
[5] Brigham and Women's Hospital and Harvard Medical School,undefined
[6] Beijing Shijitan Hospital of Capital Medical University,undefined
[7] Albert Einstein College of Medicine of Yeshiva University,undefined
[8] BCMB Allied Program,undefined
[9] Weill Cornell Medical College,undefined
来源
Cell Research | 2014年 / 24卷
关键词
entosis; cadherin; Rho GTPase; actomyosin; p190A RhoGAP; tumor suppression;
D O I
暂无
中图分类号
学科分类号
摘要
Cell engulfment typically targets dead or dying cells for clearance from metazoan tissues. However, recent evidence demonstrates that live cells can also be targeted and that engulfment can cause cell death. Entosis is one mechanism proposed to mediate the engulfment and killing of live tumor cells by their neighbors, an activity often referred to as cell cannibalism. Here we report that the expression of exogenous epithelial cadherin proteins (E- or P-cadherin) in human breast tumor cells lacking endogenous expression of epithelial cadherins induces entosis and inhibits transformed growth. Entosis induced by cadherin expression is associated with the polarized distribution of Rho and Rho-kinase (ROCK) activity within entotic cells, which is dependent on p190A RhoGAP activity. ROCK inhibition or downregulation of p190A RhoGAP expression reduces entosis and increases the transformed growth of epithelial cadherin-expressing tumor cells. These data define new cell systems for the study of entosis, and identify entosis as a mechanism of cell cannibalism that is induced by the establishment of epithelial adhesion and inhibits transformed growth.
引用
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页码:1288 / 1298
页数:10
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