Research Papers:

Estrogen-activated MDM2 disrupts mammary tissue architecture through a p53-independent pathway

Nandini Kundu, Angelika Brekman, Jun Yeob Kim, Gu Xiao, Chong Gao and Jill Bargonetti _

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Oncotarget. 2017; 8:47916-47930. https://doi.org/10.18632/oncotarget.18147

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Nandini Kundu1,2, Angelika Brekman1,3, Jun Yeob Kim1, Gu Xiao1, Chong Gao1,2 and Jill Bargonetti1,2,3,4

1The Department of Biological Sciences Hunter College, City University of New York, New York, NY 10065, USA

2PhD Program in Biology, The Graduate Center, City University of New York, New York, NY 10016, USA

3PhD Program in Biochemistry, The Graduate Center, City University of New York, New York, NY 10016, USA

4Department of Cell and Developmental Biology, Weill Cornell Medical College of Cornell University, New York, NY 10065, USA

Correspondence to:

Jill Bargonetti, email: bargonetti@genectr.hunter.cuny.edu

Keywords: p53, MDM2, estrogen receptor, Rb, E2F1

Received: September 07, 2016    Accepted: April 29, 2017    Published: May 24, 2017


The Cancer Genome Atlas (TCGA) data indicate that high MDM2 expression correlates with all subtypes of breast cancer. Overexpression of MDM2 drives breast oncogenesis in the presence of wild-type or mutant p53 (mtp53). Importantly, estrogen-receptor positive (ER+) breast cancers overexpress MDM2 and estrogen mediates this expression. We previously demonstrated that this estrogen-MDM2 axis activates the proliferation of breast cancer cell lines T47D (mtp53 L194F) and MCF7 (wild-type p53) in a manner independent of increased degradation of wild-type p53 (ie, p53-independently). Herein we present data supporting the role of the estrogen-MDM2 axis in regulating cell proliferation and mammary tissue architecture of MCF7 and T47D cells in a p53-independent manner. Inducible shRNA mediated MDM2 knockdown inhibited colony formation in soft agar, decreased mass size and induced lumen formation in matrigel and also significantly reduced mitosis as seen by decreased phospho-histone H3 positive cells. The knockdown of MDM2 in both cell lines decreased Rb phosphorylation and the level of E2F1 protein. This signaling was through the estrogen receptor because fulvestrant (a selective estrogen receptor degrader) decreased MDM2 protein levels and decreased phosphorylation of Rb. Taken together these data indicate that in some ER+ breast cancers the estrogen-MDM2-Rb-E2F1 axis is a central hub for estrogen-mediated p53-independent signal transduction. This is the first indication that estrogen signaling utilizes the estrogen-MDM2 axis to provoke phosphorylation of Rb and increase E2F1 while promoting abnormal mammary architecture.

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