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Publication : Constitutive activation of RANK disrupts mammary cell fate leading to tumorigenesis.

First Author  Pellegrini P Year  2013
Journal  Stem Cells Volume  31
Issue  9 Pages  1954-65
PubMed ID  23766243 Mgi Jnum  J:202714
Mgi Id  MGI:5521260 Doi  10.1002/stem.1454
Citation  Pasquale P, et al. (2013) Constitutive activation of RANK disrupts mammary cell fate leading to tumorigenesis. Stem Cells 31(9):1954-65
abstractText  Receptor Activator of NF-kappa B (RANK) pathway controls mammary gland development in mice but its role in mammary stem cell fate remains undefined. We show that constitutive RANK signaling expands luminal and basal mammary compartments including mammary stem and luminal progenitor cell pools and interferes with the generation of CD61+ and Sca1+ luminal cells and Elf5 expression. Impaired mammary cell commitment upon RANK overexpression leads to the accumulation of progenitors including K14+K8+ bipotent cells and the formation of heterogeneous tumors containing hyperplastic basal, luminal, and progenitor cells. RANK expression increases in wild-type mammary epithelia with age and parity, and spontaneous preneoplastic lesions express RANK and accumulate K14+K8+ cells. In human breast tumors, high RANK expression levels are also associated with altered mammary differentiation. These results suggest that increased RANK signaling interferes with mammary cell commitment, contributing to breast carcinogenesis.
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