| Literature DB >> 32359398 |
Yael Ben-Nun1, Hyuk-Soo Seo2, Edward P Harvey1, Zachary J Hauseman1, Thomas E Wales3, Catherine E Newman1, Ann M Cathcart1, John R Engen3, Sirano Dhe-Paganon2, Loren D Walensky4.
Abstract
p53 is a critical tumor-suppressor protein that guards the human genome against mutations by inducing cell-cycle arrest or apoptosis. Cancer cells subvert p53 by deletion, mutation, or overexpression of the negative regulators HDM2 and HDMX. For tumors that retain wild-type p53, its reactivation by pharmacologic targeting of HDM2 and/or HDMX represents a promising strategy, with a series of selective small-molecule HDM2 inhibitors and a dual HDM2/HDMX stapled-peptide inhibitor being evaluated in clinical trials. Because selective HDM2 targeting can cause hematologic toxicity, selective HDMX inhibitors could provide an alternative p53-reactivation strategy, but clinical candidates remain elusive. Here, we applied a mutation-scanning approach to uncover p53-based stapled peptides that are selective for HDMX. Crystal structures of stapled-peptide/HDMX complexes revealed a molecular mechanism for the observed specificity, which was validated by HDMX mutagenesis. Thus, we provide a blueprint for the development of HDMX-selective inhibitors to dissect and target the p53/HDMX interaction.Entities:
Keywords: HDM2/MDM2; HDMX/MDMX/MDM4; SAH-p53; cancer; p53; selective; stapled peptide; structure; targeting; therapeutic
Year: 2020 PMID: 32359398 PMCID: PMC7427690 DOI: 10.1016/j.str.2020.04.011
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006