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Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target
In diseases where epigenetic mechanisms are changed, such as cancer, many genes show altered gene expression and inhibited genes become activated. Human endogenous retrovirus type K (HERV-K) expression is usually inhibited in normal cells from healthy adults. In tumor cells, however, HERV-K mRNA exp...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412025/ https://www.ncbi.nlm.nih.gov/pubmed/32640516 http://dx.doi.org/10.3390/v12070726 |
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author | Curty, Gislaine Marston, Jez L. de Mulder Rougvie, Miguel Leal, Fabio E. Nixon, Douglas F. Soares, Marcelo A. |
author_facet | Curty, Gislaine Marston, Jez L. de Mulder Rougvie, Miguel Leal, Fabio E. Nixon, Douglas F. Soares, Marcelo A. |
author_sort | Curty, Gislaine |
collection | PubMed |
description | In diseases where epigenetic mechanisms are changed, such as cancer, many genes show altered gene expression and inhibited genes become activated. Human endogenous retrovirus type K (HERV-K) expression is usually inhibited in normal cells from healthy adults. In tumor cells, however, HERV-K mRNA expression has been frequently documented to increase. Importantly, HERV-K-derived proteins can act as tumor-specific antigens, a class of neoantigens, and induce immune responses in different types of cancer. In this review, we describe the function of the HERV-K HML-2 subtype in carcinogenesis as biomarkers, and their potential as targets for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-7412025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74120252020-08-25 Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target Curty, Gislaine Marston, Jez L. de Mulder Rougvie, Miguel Leal, Fabio E. Nixon, Douglas F. Soares, Marcelo A. Viruses Review In diseases where epigenetic mechanisms are changed, such as cancer, many genes show altered gene expression and inhibited genes become activated. Human endogenous retrovirus type K (HERV-K) expression is usually inhibited in normal cells from healthy adults. In tumor cells, however, HERV-K mRNA expression has been frequently documented to increase. Importantly, HERV-K-derived proteins can act as tumor-specific antigens, a class of neoantigens, and induce immune responses in different types of cancer. In this review, we describe the function of the HERV-K HML-2 subtype in carcinogenesis as biomarkers, and their potential as targets for cancer immunotherapy. MDPI 2020-07-06 /pmc/articles/PMC7412025/ /pubmed/32640516 http://dx.doi.org/10.3390/v12070726 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Curty, Gislaine Marston, Jez L. de Mulder Rougvie, Miguel Leal, Fabio E. Nixon, Douglas F. Soares, Marcelo A. Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target |
title | Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target |
title_full | Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target |
title_fullStr | Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target |
title_full_unstemmed | Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target |
title_short | Human Endogenous Retrovirus K in Cancer: A Potential Biomarker and Immunotherapeutic Target |
title_sort | human endogenous retrovirus k in cancer: a potential biomarker and immunotherapeutic target |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412025/ https://www.ncbi.nlm.nih.gov/pubmed/32640516 http://dx.doi.org/10.3390/v12070726 |
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