Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/69314
Title: Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer.
Author: Maxwell, Christopher A.
Gomez-Baldó, Laia
Bonifaci, Núria
Guinó, Elisabet
Català, Isabel
Petit, Anna
Aguilar, Helena
Villanueva Garatachea, Alberto
Aytes, Alvaro
Serra-Musach, Jordi
Aiza, Gemma
Brunet, Joan
Castellsagué, Joan
Martrat, Griselda
Urruticoechea, Ander
Blanco Guillermo, Ignacio
Lázaro García, Conxi
Capellá, G. (Gabriel)
Genestar, Miquel Àngel
Moreno Aguado, Víctor
Keywords: Càncer de mama
Cèl·lules epitelials
Oncogens
Breast cancer
Epithelial cells
Oncogenes
Issue Date: 2011
Publisher: Public Library of Science (PLoS)
Abstract: Differentiated mammary epithelium shows apicobasal polarity, and loss of tissue organization is an early hallmark of breast carcinogenesis. In BRCA1 mutation carriers, accumulation of stem and progenitor cells in normal breast tissue and increased risk of developing tumors of basal-like type suggest that BRCA1 regulates stem/progenitor cell proliferation and differentiation. However, the function of BRCA1 in this process and its link to carcinogenesis remain unknown. Here we depict a molecular mechanism involving BRCA1 and RHAMM that regulates apicobasal polarity and, when perturbed, may increase risk of breast cancer. Starting from complementary genetic analyses across families and populations, we identified common genetic variation at the low-penetrance susceptibility HMMR locus (encoding for RHAMM) that modifies breast cancer risk among BRCA1, but probably not BRCA2, mutation carriers: n = 7,584, weighted hazard ratio (wHR) = 1.09 (95% CI 1.02-1.16), ptrend = 0.017; and n = 3,965, wHR = 1.04 (95% CI 0.94-1.16), ptrend = 0.43; respectively. Subsequently, studies of MCF10A apicobasal polarization revealed a central role for BRCA1 and RHAMM, together with AURKA and TPX2, in essential reorganization of microtubules. Mechanistically, reorganization is facilitated by BRCA1 and impaired by AURKA, which is regulated by negative feedback involving RHAMM and TPX2. Taken together, our data provide fundamental insight into apicobasal polarization through BRCA1 function, which may explain the expanded cell subsets and characteristic tumor type accompanying BRCA1 mutation, while also linking this process to sporadic breast cancer through perturbation of HMMR/RHAMM.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pbio.1001199
It is part of: PLoS Biology, 2011, vol. 9, num. 11, p. e1001199
Related resource: http://dx.doi.org/10.1371/journal.pbio.1001199
URI: http://hdl.handle.net/2445/69314
ISSN: 1544-9173
Appears in Collections:Articles publicats en revistes (Patologia i Terapèutica Experimental)
Articles publicats en revistes (Ciències Clíniques)

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