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Epigenetically deregulated microRNA-375 is involved in a positive feedback loop with estrogen receptor alpha in breast cancer cells.

Authors :
de Souza Rocha Simonini P
Breiling A
Gupta N
Malekpour M
Youns M
Omranipour R
Malekpour F
Volinia S
Croce CM
Najmabadi H
Diederichs S
Sahin O
Mayer D
Lyko F
Hoheisel JD
Riazalhosseini Y
Source :
Cancer research [Cancer Res] 2010 Nov 15; Vol. 70 (22), pp. 9175-84. Date of Electronic Publication: 2010 Oct 26.
Publication Year :
2010

Abstract

Estrogen receptor α (ERα) upregulation causes abnormal cell proliferation in about two thirds of breast cancers, yet understanding of the underlying mechanisms remains incomplete. Here, we show that high expression of the microRNA miR-375 in ERα-positive breast cell lines is a key driver of their proliferation. miR-375 overexpression was caused by loss of epigenetic marks including H3K9me2 and local DNA hypomethylation, dissociation of the transcriptional repressor CTCF from the miR-375 promoter, and interactions of ERα with regulatory regions of miR-375. Inhibiting miR-375 in ERα-positive MCF-7 cells resulted in reduced ERα activation and cell proliferation. A combination of expression profiling from tumor samples and miRNA target prediction identified RASD1 as a potential miR-375 target. Mechanistic investigations revealed that miR-375 regulates RASD1 by targeting the 3' untranslated region in RASD1 mRNA. Additionally, we found that RASD1 negatively regulates ERα expression. Our findings define a forward feedback pathway in control of ERα expression, highlighting new strategies to treat ERα-positive invasive breast tumors.<br /> (Copyright © 2010 AACR.)

Details

Language :
English
ISSN :
1538-7445
Volume :
70
Issue :
22
Database :
MEDLINE
Journal :
Cancer research
Publication Type :
Academic Journal
Accession number :
20978187
Full Text :
https://doi.org/10.1158/0008-5472.CAN-10-1318