Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/71476
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: FOXP3 and FOXP3-regulated microRNAs suppress SATB1 in breast cancer cells
Author: McInnes, N.
Sadlon, T.
Brown, C.
Pederson, S.
Beyer, M.
Schultze, J.
McColl, S.
Goodall, G.
Barry, S.
Citation: Oncogene, 2012; 31(8):1045-1054
Publisher: Nature Publishing Group
Issue Date: 2012
ISSN: 0950-9232
1476-5594
Statement of
Responsibility: 
N McInnes, TJ Sadlon, CY Brown, S Pederson, M Beyer, JL Schultze, S McColl, GJ Goodall and SC Barry
Abstract: The transcription factor FOXP3 has been identified as a tumour suppressor in the breast and prostate epithelia, but little is known about its specific mechanism of action. We have identified a feed-forward regulatory loop in which FOXP3 suppresses the expression of the oncogene SATB1. In particular, we demonstrate that SATB1 is not only a direct target of FOXP3 repression, but that FOXP3 also induces two miRs, miR-7 and miR-155, which specifically target the 3′-UTR of SATB1 to further regulate its expression. We conclude that FOXP3-regulated miRs form part of the mechanism by which FOXP3 prevents the transformation of the healthy breast epithelium to a cancerous phenotype. Approaches aimed at restoring FOXP3 function and the miRs it regulates could help provide new approaches to target breast cancer.
Keywords: SATB1; FOXP3; microRNA; gene regulation networks; breast cancer; tumour suppressor
Rights: © 2012 Macmillan Publishers Limited
RMID: 0020112141
DOI: 10.1038/onc.2011.293
Grant ID: http://purl.org/au-research/grants/nhmrc/565314
Appears in Collections:Paediatrics publications

Files in This Item:
File Description SizeFormat 
hdl_71476.pdfAccepted version1.4 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.