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The FBXW7 tumor suppressor inhibits breast cancer proliferation and promotes apoptosis by targeting MTDH for degradation

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Xi Chen, Xingyu Li, Min Long, Xi Wang, Zhaowei Gao, Ying Cui, Jihong Ren, Zhe Zhang, Chong Liu,  Ke Dong,  Huizhong Zhang

Abstract:

MTDH is an oncoprotein and is expressed at high levels in a wide variety of human carcinomas, which represents an important genetic determinant and regulates multiple events in tumorigenesis. MTDH promotes breast cancer cell proliferation and tumorigenesis through the activation of numerous signaling pathways. Currently, the mechanism regulating MTDH expression is poorly understood. Here we identified that FBXW7, a component of E3 ubiquitin ligase, targets MTDH for ubiquitin-mediated degradation. Forced overexpression of FBXW7 could decrease the level of MTDH protein, and inhibition of endogenous FBXW7 expression remarkably increases the MTDH protein abundances. More importantly, overexpression of FBXW7 could lead to proliferation arrest and apoptosis in breast cancer cells through targeting MTDH degradation. These data suggested that FBXW7, a tumor suppressor, inhibits breast cancer cell proliferation and promotes apoptosis at least partially through targeting MTDH for proteolysis. This new regulatory mechanism of MTDH by FBXW7 represented a new pathway for malignant phenotype turnover in human breast cancer.

Received date: 02/28/2017

Accepted date: 06/10/2017

Ahead of print publish date: 03/13/2018

Issue: 2/2018

Volume: 65

Pages: 201 — 209

Keywords: MTDH, FBXW7, Ubiquitin-proteasome degradation, cell proliferation, cell apoptosis, breast cancer

Supplementary files:
Supplementary figure - TE.tif

DOI: 10.4149/neo_2018_170228N149

Pubmed

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