| Literature DB >> 31202462 |
Seok Yun Jung1, Jisoo Yun1, Seong Jang Kim2, Songhwa Kang1, Da Yeon Kim1, Yeon Ju Kim1, Ji Hye Park1, Woong Bi Jang1, Seung Taek Ji1, Jong Seong Ha1, Le Thi Hong Van1, Ly Thanh Truong Giang1, Vinoth Kumar Rethineswaran1, Dong Hwan Kim3, Parkyong Song4, Sang-Mo Kwon5.
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.Entities:
Keywords: Anterior gradient protein 2 homolog (AGR2); Breast cancer; E-box sequence; Twist-related protein 1 (Twist1)
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Year: 2019 PMID: 31202462 DOI: 10.1016/j.bbrc.2019.05.191
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575