FoxM1 Regulates Mammary Luminal Cell Fate

摘要

SummaryElevated 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.Graphical AbstractFigure optionsView in workspaceDownload full-size imageDownload as PowerPoint slideHighlights? Increased FOXM1 leads to an expansion of mammary stem and progenitor pools ? Deletion of FoxM1 in virgin mice causes accumulation of the differentiated luminal cells ? FOXM1 acts as a transcriptional repressor of GATA-3 by promoting DNA methylation ? FOXM1 represses GATA-3 in an Rb-dependent manner.