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Genetic alterations and epigenetic alterations of cancer-associated fibroblasts

Cancer-associated fibroblasts (CAFs) are one major type of component identified in the tumor microenvironment. Studies have focused on the genetic and epigenetic status of CAFs, since they are critical in tumor progression and differ phenotypically and functionally from normal fibroblasts. The prese...

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Detalles Bibliográficos
Autores principales: Du, Heng, Che, Guowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245074/
https://www.ncbi.nlm.nih.gov/pubmed/28123515
http://dx.doi.org/10.3892/ol.2016.5451
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author Du, Heng
Che, Guowei
author_facet Du, Heng
Che, Guowei
author_sort Du, Heng
collection PubMed
description Cancer-associated fibroblasts (CAFs) are one major type of component identified in the tumor microenvironment. Studies have focused on the genetic and epigenetic status of CAFs, since they are critical in tumor progression and differ phenotypically and functionally from normal fibroblasts. The present review summarizes the recent achievements in understanding the gene profiles of CAFs and pays special attention to their possible epigenetic alterations. A total of 7 possible genetic alterations and epigenetic changes in CAFs are discussed, including gene differential expression, karyotype analysis, gene copy number variation, loss of heterozygosis, allelic imbalance, microsatellite instability, post-transcriptional control and DNA methylation. These genetic and epigenetic characteristics are hypothesized to provide a deep understanding of CAFs and a perspective on their clinical significance.
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spelling pubmed-52450742017-01-25 Genetic alterations and epigenetic alterations of cancer-associated fibroblasts Du, Heng Che, Guowei Oncol Lett Review Cancer-associated fibroblasts (CAFs) are one major type of component identified in the tumor microenvironment. Studies have focused on the genetic and epigenetic status of CAFs, since they are critical in tumor progression and differ phenotypically and functionally from normal fibroblasts. The present review summarizes the recent achievements in understanding the gene profiles of CAFs and pays special attention to their possible epigenetic alterations. A total of 7 possible genetic alterations and epigenetic changes in CAFs are discussed, including gene differential expression, karyotype analysis, gene copy number variation, loss of heterozygosis, allelic imbalance, microsatellite instability, post-transcriptional control and DNA methylation. These genetic and epigenetic characteristics are hypothesized to provide a deep understanding of CAFs and a perspective on their clinical significance. D.A. Spandidos 2017-01 2016-11-30 /pmc/articles/PMC5245074/ /pubmed/28123515 http://dx.doi.org/10.3892/ol.2016.5451 Text en Copyright: © Du et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Du, Heng
Che, Guowei
Genetic alterations and epigenetic alterations of cancer-associated fibroblasts
title Genetic alterations and epigenetic alterations of cancer-associated fibroblasts
title_full Genetic alterations and epigenetic alterations of cancer-associated fibroblasts
title_fullStr Genetic alterations and epigenetic alterations of cancer-associated fibroblasts
title_full_unstemmed Genetic alterations and epigenetic alterations of cancer-associated fibroblasts
title_short Genetic alterations and epigenetic alterations of cancer-associated fibroblasts
title_sort genetic alterations and epigenetic alterations of cancer-associated fibroblasts
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245074/
https://www.ncbi.nlm.nih.gov/pubmed/28123515
http://dx.doi.org/10.3892/ol.2016.5451
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