Cargando…

The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment

The prognosis for patients with cancers known for a highly activated stromal reaction, including diffuse‐type (scirrhous) gastric cancer, consensus molecular subtype 4 (CMS4) colorectal cancer, and pancreatic ductal adenocarcinoma, is extremely poor. To explore the resistance of conventional therapy...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamamoto, Yurie, Kasashima, Hiroaki, Fukui, Yasuhiro, Tsujio, Gen, Yashiro, Masakazu, Maeda, Kiyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807521/
https://www.ncbi.nlm.nih.gov/pubmed/36197901
http://dx.doi.org/10.1111/cas.15609
_version_ 1784862737921212416
author Yamamoto, Yurie
Kasashima, Hiroaki
Fukui, Yasuhiro
Tsujio, Gen
Yashiro, Masakazu
Maeda, Kiyoshi
author_facet Yamamoto, Yurie
Kasashima, Hiroaki
Fukui, Yasuhiro
Tsujio, Gen
Yashiro, Masakazu
Maeda, Kiyoshi
author_sort Yamamoto, Yurie
collection PubMed
description The prognosis for patients with cancers known for a highly activated stromal reaction, including diffuse‐type (scirrhous) gastric cancer, consensus molecular subtype 4 (CMS4) colorectal cancer, and pancreatic ductal adenocarcinoma, is extremely poor. To explore the resistance of conventional therapy for those refractory cancers, detailed classification and investigation of the different subsets of cancer‐associated fibroblasts (CAFs) involved are needed. Recent studies with a single‐cell transcriptomics strategy (single‐cell RNA‐seq) have demonstrated that CAF subpopulations contain different origins and marker proteins with the capacity to either promote or suppress cancer progression. Through multiple signaling pathways, CAFs can promote tumor growth, metastasis, and angiogenesis with extracellular matrix (ECM) remodeling; they can also interact with tumor‐infiltrating immune cells and modulate the antitumor immunological state in the tumor microenvironment (TME). Here, we review the recent literature on the various subpopulations of CAFs to improve our understanding of the cell‐cell interactions in the TME and highlight future avenues for CAF‐targeted therapy.
format Online
Article
Text
id pubmed-9807521
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-98075212023-01-04 The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment Yamamoto, Yurie Kasashima, Hiroaki Fukui, Yasuhiro Tsujio, Gen Yashiro, Masakazu Maeda, Kiyoshi Cancer Sci Review Articles The prognosis for patients with cancers known for a highly activated stromal reaction, including diffuse‐type (scirrhous) gastric cancer, consensus molecular subtype 4 (CMS4) colorectal cancer, and pancreatic ductal adenocarcinoma, is extremely poor. To explore the resistance of conventional therapy for those refractory cancers, detailed classification and investigation of the different subsets of cancer‐associated fibroblasts (CAFs) involved are needed. Recent studies with a single‐cell transcriptomics strategy (single‐cell RNA‐seq) have demonstrated that CAF subpopulations contain different origins and marker proteins with the capacity to either promote or suppress cancer progression. Through multiple signaling pathways, CAFs can promote tumor growth, metastasis, and angiogenesis with extracellular matrix (ECM) remodeling; they can also interact with tumor‐infiltrating immune cells and modulate the antitumor immunological state in the tumor microenvironment (TME). Here, we review the recent literature on the various subpopulations of CAFs to improve our understanding of the cell‐cell interactions in the TME and highlight future avenues for CAF‐targeted therapy. John Wiley and Sons Inc. 2022-10-19 /pmc/articles/PMC9807521/ /pubmed/36197901 http://dx.doi.org/10.1111/cas.15609 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Yamamoto, Yurie
Kasashima, Hiroaki
Fukui, Yasuhiro
Tsujio, Gen
Yashiro, Masakazu
Maeda, Kiyoshi
The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment
title The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment
title_full The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment
title_fullStr The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment
title_full_unstemmed The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment
title_short The heterogeneity of cancer‐associated fibroblast subpopulations: Their origins, biomarkers, and roles in the tumor microenvironment
title_sort heterogeneity of cancer‐associated fibroblast subpopulations: their origins, biomarkers, and roles in the tumor microenvironment
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807521/
https://www.ncbi.nlm.nih.gov/pubmed/36197901
http://dx.doi.org/10.1111/cas.15609
work_keys_str_mv AT yamamotoyurie theheterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT kasashimahiroaki theheterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT fukuiyasuhiro theheterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT tsujiogen theheterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT yashiromasakazu theheterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT maedakiyoshi theheterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT yamamotoyurie heterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT kasashimahiroaki heterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT fukuiyasuhiro heterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT tsujiogen heterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT yashiromasakazu heterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment
AT maedakiyoshi heterogeneityofcancerassociatedfibroblastsubpopulationstheiroriginsbiomarkersandrolesinthetumormicroenvironment