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Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment

Tumor- or cancer-associated fibroblasts (CAFs) are one of the most abundant stromal cell types in different carcinomas and comprise a heterogeneous cell population. Classically, CAFs are assigned with pro-tumorigenic effects stimulating tumor growth and progression. More recent studies demonstrated...

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Detalles Bibliográficos
Autor principal: Augsten, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973916/
https://www.ncbi.nlm.nih.gov/pubmed/24734219
http://dx.doi.org/10.3389/fonc.2014.00062
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author Augsten, Martin
author_facet Augsten, Martin
author_sort Augsten, Martin
collection PubMed
description Tumor- or cancer-associated fibroblasts (CAFs) are one of the most abundant stromal cell types in different carcinomas and comprise a heterogeneous cell population. Classically, CAFs are assigned with pro-tumorigenic effects stimulating tumor growth and progression. More recent studies demonstrated also tumor-inhibitory effects of CAFs suggesting that tumor-residing fibroblasts exhibit a similar degree of plasticity as other stromal cell types. Reciprocal interactions with the tumor milieu and different sources of origin are emerging as two important factors underlying CAF heterogeneity. This review highlights recent advances in our understanding of CAF biology and proposes to expand the term of cellular “polarization,” previously introduced to describe different activation states of various immune cells, onto CAFs to reflect their phenotypic diversity.
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spelling pubmed-39739162014-04-14 Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment Augsten, Martin Front Oncol Oncology Tumor- or cancer-associated fibroblasts (CAFs) are one of the most abundant stromal cell types in different carcinomas and comprise a heterogeneous cell population. Classically, CAFs are assigned with pro-tumorigenic effects stimulating tumor growth and progression. More recent studies demonstrated also tumor-inhibitory effects of CAFs suggesting that tumor-residing fibroblasts exhibit a similar degree of plasticity as other stromal cell types. Reciprocal interactions with the tumor milieu and different sources of origin are emerging as two important factors underlying CAF heterogeneity. This review highlights recent advances in our understanding of CAF biology and proposes to expand the term of cellular “polarization,” previously introduced to describe different activation states of various immune cells, onto CAFs to reflect their phenotypic diversity. Frontiers Media S.A. 2014-03-27 /pmc/articles/PMC3973916/ /pubmed/24734219 http://dx.doi.org/10.3389/fonc.2014.00062 Text en Copyright © 2014 Augsten. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Augsten, Martin
Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment
title Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment
title_full Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment
title_fullStr Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment
title_full_unstemmed Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment
title_short Cancer-Associated Fibroblasts as Another Polarized Cell Type of the Tumor Microenvironment
title_sort cancer-associated fibroblasts as another polarized cell type of the tumor microenvironment
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973916/
https://www.ncbi.nlm.nih.gov/pubmed/24734219
http://dx.doi.org/10.3389/fonc.2014.00062
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