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Immune pressures drive the promoter hypermethylation of neoantigen genes

Cancer cells with strong immunogenicity are susceptible for elimination by cancer immunoediting, while the subpopulations with weak immunogenicity survive. As a result, a subset of cancer cells evade the immune attack and evolve into overt clinical lesions. During cancer evolution, it has been well...

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Detalles Bibliográficos
Autores principales: Yi, Ming, Dong, Bing, Chu, Qian, Wu, Kongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884785/
https://www.ncbi.nlm.nih.gov/pubmed/31799063
http://dx.doi.org/10.1186/s40164-019-0156-7
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author Yi, Ming
Dong, Bing
Chu, Qian
Wu, Kongming
author_facet Yi, Ming
Dong, Bing
Chu, Qian
Wu, Kongming
author_sort Yi, Ming
collection PubMed
description Cancer cells with strong immunogenicity are susceptible for elimination by cancer immunoediting, while the subpopulations with weak immunogenicity survive. As a result, a subset of cancer cells evade the immune attack and evolve into overt clinical lesions. During cancer evolution, it has been well established that multiple alterations such as the dysfunction of antigen presentation machinery and the upregulation of immunosuppressive signals (e.g. PD-L1) play important roles in immune escape. Recently, promoter hypermethylation of neoantigen genes has been proposed to be a vital mechanism of immunoediting. This epigenetically mediated immune evasion enriches the mechanisms of carcinogenesis.
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spelling pubmed-68847852019-12-03 Immune pressures drive the promoter hypermethylation of neoantigen genes Yi, Ming Dong, Bing Chu, Qian Wu, Kongming Exp Hematol Oncol Editorial Cancer cells with strong immunogenicity are susceptible for elimination by cancer immunoediting, while the subpopulations with weak immunogenicity survive. As a result, a subset of cancer cells evade the immune attack and evolve into overt clinical lesions. During cancer evolution, it has been well established that multiple alterations such as the dysfunction of antigen presentation machinery and the upregulation of immunosuppressive signals (e.g. PD-L1) play important roles in immune escape. Recently, promoter hypermethylation of neoantigen genes has been proposed to be a vital mechanism of immunoediting. This epigenetically mediated immune evasion enriches the mechanisms of carcinogenesis. BioMed Central 2019-11-29 /pmc/articles/PMC6884785/ /pubmed/31799063 http://dx.doi.org/10.1186/s40164-019-0156-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Editorial
Yi, Ming
Dong, Bing
Chu, Qian
Wu, Kongming
Immune pressures drive the promoter hypermethylation of neoantigen genes
title Immune pressures drive the promoter hypermethylation of neoantigen genes
title_full Immune pressures drive the promoter hypermethylation of neoantigen genes
title_fullStr Immune pressures drive the promoter hypermethylation of neoantigen genes
title_full_unstemmed Immune pressures drive the promoter hypermethylation of neoantigen genes
title_short Immune pressures drive the promoter hypermethylation of neoantigen genes
title_sort immune pressures drive the promoter hypermethylation of neoantigen genes
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884785/
https://www.ncbi.nlm.nih.gov/pubmed/31799063
http://dx.doi.org/10.1186/s40164-019-0156-7
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