| Literature DB >> 31727256 |
Lucillia Bezu1, Alejandra Wu Chuang2, Juliette Humeau2, Guido Kroemer3, Oliver Kepp4.
Abstract
Immunogenic cell death (ICD) is a particular modality of cell death that can be triggered by selected anticancer chemotherapeutics. Tumor cells undergoing ICD can induce an adaptive anticancer immune response that targets residual cancer cells with the same antigenic profile. The activation of a full-blown immune response against the tumor antigen is preceded by the release or exposure of danger associated molecular patterns (DAMPs) by tumor cells that stimulate the attraction, activation and maturation of dendritic cells and eventually the antigen-specific priming of cytotoxic T lymphocytes (CTLs). The phosphorylation of the eukaryotic translation initiation factor (EIF2A) is a pathognomonic characteristic of ICD, which governs the release/exposure of DAMPs such as ATP and calreticulin and thus the immunogenicity of cell death. Here we describe techniques to detect eIF2alpha phosphorylation for the assessment of ICD.Entities:
Keywords: Cancer; Endoplasmic reticulum stress; Immune response; Mitoxantrone; Oxaliplatin
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Year: 2019 PMID: 31727256 DOI: 10.1016/bs.mie.2019.04.010
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600