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Basic helix-loop-helix transcription factor Twist1 is a novel regulator of anterior gradient protein 2 homolog (AGR2) in breast cancer.

Authors :
Jung, Seok Yun
Yun, Jisoo
Kim, Seong Jang
Kang, Songhwa
Kim, Da Yeon
Kim, Yeon Ju
Park, Ji Hye
Jang, Woong Bi
Ji, Seung Taek
Ha, Jong Seong
Hong Van, Le Thi
Truong Giang, Ly Thanh
Rethineswaran, Vinoth Kumar
Kim, Dong Hwan
Song, Parkyong
Kwon, Sang-Mo
Source :
Biochemical & Biophysical Research Communications. Aug2019, Vol. 516 Issue 1, p149-156. 8p.
Publication Year :
2019

Abstract

Anterior gradient protein 2 homolog (AGR2) belongs to the disulfide isomerase family of endoplasmic reticulum proteins. Itis overexpressed in several types of solid tumors, including tumors of the prostate, lung, and pancreas. However, the role of AGR2 in breast cancer and the regulatory mechanisms underlying AGR2 protein expressionare not fullyunderstood. We demonstrated that AGR2 levels are increased under hypoxic conditions and in breast cancer tumors. Mechanistically, Twist1 binds to, and activates the AGR2 promoter via an E-box sequence. Under hypoxic conditions, the increased expression of ARG2 is attenuated when Twist1 levels are reduced by shRNA. Conversely, Twist1 overexpression fully reverses decreased AGR2 levels upon HIF-1α knockdown. Notably, AGR2 is required for Twist1-induced proliferation, migration, and invasion of breast cancer cells. Collectively, these findings extend our understanding of AGR2 regulation in breast cancer and may contribute to development of Twist1-AGR2 targeting therapeutics for breast cancer. • HIF-1α/Twist1 is a crucial regulatory pathway for AGR2 expression in breast cancer cells. • Twist1 increases AGR2 promoter activity via direct binding to E-box motif. • AGR2 is a critical oncogenic protein in Twist1 mediated breast cancer cell survival and metastasis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
516
Issue :
1
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
137304363
Full Text :
https://doi.org/10.1016/j.bbrc.2019.05.191