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Endothelin Promotes Colorectal Tumorigenesis by Activating YAP/TAZ.


ABSTRACT: Endothelin receptor A (ETAR) promotes tumorigenesis by stimulating cell proliferation, migration, and survival. However, the mechanism of ETAR in promoting tumor growth is largely unknown. In this study, we demonstrate that ETAR stimulates colon cell proliferation, migration, and tumorigenesis through the activation of YAP/TAZ, two transcription coactivators of the Hippo tumor suppressor pathway. Endothelin-1 treatment induced YAP/TAZ dephosphorylation, nuclear accumulation, and transcriptional activation in multiple colon cancer cells. ETAR stimulation acted via downstream G-protein G?q/11 and Rho GTPase to suppress the Hippo pathway, thus leading to YAP/TAZ activation, which was required for ETAR-induced tumorigenesis. Overall, these results indicate a critical role of the YAP/TAZ axis in ETAR signaling. Cancer Res; 77(9); 2413-23. ©2017 AACR.

SUBMITTER: Wang Z 

PROVIDER: S-EPMC6724531 | biostudies-literature | 2017 May

REPOSITORIES: biostudies-literature

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Endothelin Promotes Colorectal Tumorigenesis by Activating YAP/TAZ.

Wang Zhen Z   Liu Peng P   Zhou Xin X   Wang Tianxiang T   Feng Xu X   Sun Yi-Ping YP   Xiong Yue Y   Yuan Hai-Xin HX   Guan Kun-Liang KL  

Cancer research 20170301 9


Endothelin receptor A (ETAR) promotes tumorigenesis by stimulating cell proliferation, migration, and survival. However, the mechanism of ETAR in promoting tumor growth is largely unknown. In this study, we demonstrate that ETAR stimulates colon cell proliferation, migration, and tumorigenesis through the activation of YAP/TAZ, two transcription coactivators of the Hippo tumor suppressor pathway. Endothelin-1 treatment induced YAP/TAZ dephosphorylation, nuclear accumulation, and transcriptional  ...[more]

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