| Literature DB >> 31597089 |
Alison Hirukawa1, Salendra Singh2, Jarey Wang3, Jonathan P Rennhack4, Matthew Swiatnicki4, Virginie Sanguin-Gendreau1, Dongmei Zuo1, Kamilia Daldoul1, Cynthia Lavoie1, Morag Park5, Eran R Andrechek4, Thomas F Westbrook6, Lyndsay N Harris7, Vinay Varadan2, Harvey W Smith8, William J Muller9.
Abstract
Monoclonal antibodies (mAbs) targeting the oncogenic receptor tyrosine kinase ERBB2/HER2, such as Trastuzumab, are the standard of care therapy for breast cancers driven by ERBB2 overexpression and activation. However, a substantial proportion of patients exhibit de novo resistance. Here, by comparing matched Trastuzumab-naive and post-treatment patient samples from a neoadjuvant trial, we link resistance with elevation of H3K27me3, a repressive histone modification catalyzed by polycomb repressor complex 2 (PRC2). In ErbB2+ breast cancer models, PRC2 silences endogenous retroviruses (ERVs) to suppress anti-tumor type-I interferon (IFN) responses. In patients, elevated H3K27me3 in tumor cells following Trastuzumab treatment correlates with suppression of interferon-driven viral defense gene expression signatures and poor response. Using an immunocompetent model, we provide evidence that EZH2 inhibitors promote interferon-driven immune responses that enhance the efficacy of anti-ErbB2 mAbs, suggesting the potential clinical benefit of epigenomic reprogramming by H3K27me3 depletion in Trastuzumab-resistant disease.Entities:
Keywords: ErbB2/HER2; PRC2; Polycomb Repressor Complex 2; Trastuzumab resistance; breast cancer; endogenous retroviruses; epigenetics; immune surveillance; transcriptional silencing; type I interferon signaling
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Year: 2019 PMID: 31597089 DOI: 10.1016/j.celrep.2019.08.105
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423