A tumor-suppressive function for Notch3 in the parous mammary gland

Notch3 promotes mammary luminal cell specification and forced Notch3 activation can induce mammary tumor formation. However, recent studies suggest a tumor-suppressive role for Notch3. Here, we report on Notch3 expression and functional analysis in the mouse mammary gland. Notch3 is expressed in the luminal compartment throughout mammary gland development, but switches to basal cells with initiation of post-lactational involution. Deletion of Notch3 caused a decrease of Notch activation in luminal cells and diminished luminal progenitors at puberty, as well as reduced alveolar progenitors during pregnancy. Parous Notch3(-/-) mammary glands developed hyperplasia with accumulation of CD24(hi)CD49f(lo) cells, some of which progressed to invasive tumors with luminal features. Notch3 deletion abolished Notch activation in basal cells during involution, accompanied by altered apoptosis and reduced brown adipocytes, leading to expansion of parity-identified mammary epithelial cells (PI-MECs). Interestingly, the postpartum microenvironment is required for the stem cell activity of Notch3(-/-) PI-MECs. Finally, high expression of NOTCH3 is associated with prolonged survival in patients with luminal breast cancer. These results highlight an unexpected tumor-suppressive function for Notch3 in the parous mammary gland through restriction of PI-MEC expansion.

Automated summary

Notch3 plays a role in promoting mammary luminal cell specification, but recent studies show it also has a tumor-suppressive function. In mouse mammary glands, Notch3 is expressed in the luminal compartment during development, but switches to basal cells after weaning. Deletion of Notch3 leads to abnormal mammary gland development and formation of tumors.