HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The estrogen-responsive Agr2 gene regulates mammary epithelial proliferation and facilitates lobuloalveolar development.

Abstract
Agr2 is a putative protein disulfide isomerase (PDI) initially identified as an estrogen-responsive gene in breast cancer cell lines. While Agr2 expression in breast cancer is positively correlated with estrogen receptor (ER) expression, it is upregulated in both hormone dependent and independent carcinomas. Several in vitro and xenograft studies have implicated Agr2 in different oncogenic features of breast cancer; however, the physiological role of Agr2 in normal mammary gland development remains to be defined. Agr2 expression is developmentally regulated in the mammary gland, with maximum expression during late pregnancy and lactation. Using a mammary gland specific knockout mouse model, we show that Agr2 facilitates normal lobuloalveolar development by regulating mammary epithelial cell proliferation; we found no effects on apoptosis in Agr2(-/-) mammary epithelial cells. Consequently, mammary glands of Agr2(-/-) females exhibit reduced expression of milk proteins, and by two weeks post-partum their pups are smaller in size. Utilizing a conditional mouse model, we show that Agr2 constitutive expression drives precocious lobuloalveolar development and increased milk protein expression in the virgin mammary gland. In vitro studies using knock down and overexpression strategies in estrogen receptor positive and negative mammary epithelial cell lines demonstrate a role for Agr2 in estradiol-induced cell proliferation. In conclusion, the estrogen-responsive Agr2, a candidate breast cancer oncogene, regulates epithelial cell proliferation and lobuloalveolar development in the mammary gland. The pro-proliferative effects of Agr2 may explain its actions in early tumorigenesis.
AuthorsSuman Verma, Michael L Salmans, Mikhail Geyfman, Hong Wang, Zhengquan Yu, Zhongxian Lu, Fang Zhao, Steven M Lipkin, Bogi Andersen
JournalDevelopmental biology (Dev Biol) Vol. 369 Issue 2 Pg. 249-60 (Sep 15 2012) ISSN: 1095-564X [Electronic] United States
PMID22819674 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • AGR2 protein, human
  • Agr2 protein, mouse
  • DNA Primers
  • Mucoproteins
  • Oncogene Proteins
  • Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Estradiol
  • Protein Disulfide-Isomerases
Topics
  • Animals
  • Apoptosis
  • Base Sequence
  • Breast Neoplasms (genetics, metabolism, pathology)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • DNA Primers (genetics)
  • Epithelial Cells (cytology, metabolism)
  • Estradiol (pharmacology)
  • Female
  • Gene Expression Regulation, Developmental
  • Humans
  • Mammary Glands, Animal (cytology, growth & development, metabolism)
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Mucoproteins (deficiency, genetics, metabolism)
  • Oncogene Proteins
  • Pregnancy
  • Protein Disulfide-Isomerases (deficiency, genetics, metabolism)
  • Proteins (antagonists & inhibitors, genetics, metabolism)
  • RNA, Messenger (genetics, metabolism)
  • RNA, Small Interfering (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: