| Literature DB >> 32938196 |
Ning Kang1, Mark Eccleston2, Pier-Luc Clermont3, Maryam Latarani4, David Kingsley Male4, Yuzhuo Wang1,5, Francesco Crea4.
Abstract
Immunotherapies are revolutionizing the clinical management of a wide range of cancers. However, intrinsic or acquired unresponsiveness to immunotherapies does occur due to the dynamic cancer immunoediting which ultimately leads to immune escape. The evolutionarily conserved histone modifier enhancer of zeste 2 (EZH2) is aberrantly overexpressed in a number of human cancers. Accumulating studies indicate that EZH2 is a main driver of cancer cells' immunoediting and mediate immune escape through downregulating immune recognition and activation, upregulating immune checkpoints and creating an immunosuppressive tumor microenvironment. In this review, we overviewed the roles of EZH2 in cancer immunoediting, the preclinical and clinical studies of current pharmacologic EZH2 inhibitors and the prospects for EZH2 inhibitor and immunotherapy combination for cancer treatment.Entities:
Keywords: EZH2; cancer immunotherapy; epigenetics; immune editing
Year: 2020 PMID: 32938196 PMCID: PMC7607396 DOI: 10.2217/epi-2020-0186
Source DB: PubMed Journal: Epigenomics ISSN: 1750-192X Impact factor: 4.778