Peer-Reviewed Journal Details
Mandatory Fields
Selcuklu, SD;Donoghue, MTA;Kerin, MJ;Spillane, C
2012
June
Biochemical And Biophysical Research Communications
Regulatory interplay between miR-21, JAG1 and 17beta-estradiol (E2) in breast cancer cells
Published
WOS: 16 ()
Optional Fields
SIGNALING PATHWAY MICRORNA TARGETS GENE-EXPRESSION DOWN-REGULATION MESSENGER-RNA ESTROGEN PROLIFERATION APOPTOSIS INVASION GROWTH
423
234
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Overexpression of the oncomir miR-21 is associated with many cancers, including breast cancer. Elevated levels of Jagged-1 (JAG1), a predicted miR-21 target, are implicated in estrogen receptor negative (ER-) breast cancer. We demonstrate (by ablation of the miR-21 binding site in the JAG1 3'UTR) that miR-21 directly targets and represses JAG1 levels in MCF-7 (ER+) breast cancer cells. MiR-21 targeting of JAG1 in MDA-MB-231 (ER-) breast cancer cells is dependent on miR-21 dosage (levels). In both cell lines, miR-21 and JAG1 expression levels were negatively correlated due to their regulatory relationship. In addition, 17beta-estradiol (E2) increases JAG1 levels by limiting (via downregulating miR-21 levels) the repressive effects of miR-21 on the JAG1 3'UTR. Our results reveal a regulatory interplay between miR-21, JAG1 and E2 that is important for advancing understanding of how the oncogenic potential of miR-21 and JAG1 manifests in different sub-types of breast cancer. (C) 2012 Elsevier Inc. All rights reserved.
0006-291X
10.1016/j.bbrc.2012.05.074
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