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FoxM1 Regulates Mammary Luminal Cell Fate
Author(s) -
Janai R. Carr,
Megan M. Kiefer,
Hyun Jung Park,
Jing Li,
Zebin Wang,
Joel Fontanarosa,
Danielle DeWaal,
Dragana Kopanja,
Elizaveta V. Benevolenskaya,
Grace Guzman,
Pradip Raychaudhuri
Publication year - 2012
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2012.05.005
Subject(s) - foxm1 , gene knockdown , biology , regulator , cancer research , repressor , microbiology and biotechnology , transcription factor , psychological repression , cellular differentiation , progenitor cell , phenotype , stem cell , genetics , cell culture , gene expression , gene
Elevated expression of FoxM1 in breast cancer correlates with an undifferentiated tumor phenotype and a negative clinical outcome. However, a role for FoxM1 in regulating mammary differentiation was not known. Here, we identify another function of FoxM1, the ability to act as a transcriptional repressor, which plays an important role in regulating the differentiation of luminal epithelial progenitors. Regeneration of mammary glands with elevated levels of FoxM1 leads to aberrant ductal morphology and expansion of the luminal progenitor pool. Conversely, knockdown of FoxM1 results in a shift toward the differentiated state. FoxM1 mediates these effects by repressing the key regulator of luminal differentiation, GATA-3. Through association with DNMT3b, FoxM1 promotes methylation of the GATA-3 promoter in an Rb-dependent manner. This study identifies FoxM1 as a critical regulator of mammary differentiation with significant implications for the development of aggressive breast cancers.

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