Inhibiting Nuclear Phospho-Progesterone Receptor Enhances Antitumor Activity of Onapristone in Uterine Cancer.

Journal Article (Journal Article)

Although progesterone receptor (PR)-targeted therapies are modestly active in patients with uterine cancer, their underlying molecular mechanisms are not well understood. The clinical use of such therapies is limited because of the lack of biomarkers that predict response to PR agonists (progestins) or PR antagonists (onapristone). Thus, understanding the underlying molecular mechanisms of action will provide an advance in developing novel combination therapies for cancer patients. Nuclear translocation of PR has been reported to be ligand-dependent or -independent. Here, we identified that onapristone, a PR antagonist, inhibited nuclear translocation of ligand-dependent or -independent (EGF) phospho-PR (S294), whereas trametinib inhibited nuclear translocation of EGF-induced phospho-PR (S294). Using orthotopic mouse models of uterine cancer, we demonstrated that the combination of onapristone and trametinib results in superior antitumor effects in uterine cancer models compared with either monotherapy. These synergistic effects are, in part, mediated through inhibiting the nuclear translocation of EGF-induced PR phosphorylation in uterine cancer cells. Targeting MAPK-dependent PR activation with onapristone and trametinib significantly inhibited tumor growth in preclinical uterine cancer models and is worthy of further clinical investigation. Mol Cancer Ther; 17(2); 464-73. ©2017 AACR.

Full Text

Duke Authors

Cited Authors

  • Huang, Y; Hu, W; Huang, J; Shen, F; Sun, Y; Ivan, C; Pradeep, S; Dood, R; Haemmerle, M; Jiang, D; Mangala, LS; Noh, K; Hansen, JM; Dalton, HJ; Previs, RA; Nagaraja, AS; McGuire, M; Jennings, NB; Broaddus, R; Coleman, RL; Sood, AK

Published Date

  • February 2018

Published In

Volume / Issue

  • 17 / 2

Start / End Page

  • 464 - 473

PubMed ID

  • 29237804

Pubmed Central ID

  • PMC5805630

Electronic International Standard Serial Number (EISSN)

  • 1538-8514

Digital Object Identifier (DOI)

  • 10.1158/1535-7163.MCT-17-0006


  • eng

Conference Location

  • United States