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Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment

Cancer-associated fibroblasts (CAFs) are the predominant components of the tumor microenvironment (TME) and influence cancer hallmarks, but without systematic investigation on their ubiquitous characteristics across different cancer types. Here, we perform pan-cancer analysis on 226 samples across 1...

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Autores principales: Luo, Han, Xia, Xuyang, Huang, Li-Bin, An, Hyunsu, Cao, Minyuan, Kim, Gyeong Dae, Chen, Hai-Ning, Zhang, Wei-Han, Shu, Yang, Kong, Xiangyu, Ren, Zhixiang, Li, Pei-Heng, Liu, Yang, Tang, Huairong, Sun, Ronghao, Li, Chao, Bai, Bing, Jia, Weiguo, Liu, Yi, Zhang, Wei, Yang, Li, Peng, Yong, Dai, Lunzhi, Hu, Hongbo, Jiang, Yong, Hu, Yiguo, Zhu, Jingqiang, Jiang, Hong, Li, Zhihui, Caulin, Carlos, Park, Jihwan, Xu, Heng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636408/
https://www.ncbi.nlm.nih.gov/pubmed/36333338
http://dx.doi.org/10.1038/s41467-022-34395-2
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author Luo, Han
Xia, Xuyang
Huang, Li-Bin
An, Hyunsu
Cao, Minyuan
Kim, Gyeong Dae
Chen, Hai-Ning
Zhang, Wei-Han
Shu, Yang
Kong, Xiangyu
Ren, Zhixiang
Li, Pei-Heng
Liu, Yang
Tang, Huairong
Sun, Ronghao
Li, Chao
Bai, Bing
Jia, Weiguo
Liu, Yi
Zhang, Wei
Yang, Li
Peng, Yong
Dai, Lunzhi
Hu, Hongbo
Jiang, Yong
Hu, Yiguo
Zhu, Jingqiang
Jiang, Hong
Li, Zhihui
Caulin, Carlos
Park, Jihwan
Xu, Heng
author_facet Luo, Han
Xia, Xuyang
Huang, Li-Bin
An, Hyunsu
Cao, Minyuan
Kim, Gyeong Dae
Chen, Hai-Ning
Zhang, Wei-Han
Shu, Yang
Kong, Xiangyu
Ren, Zhixiang
Li, Pei-Heng
Liu, Yang
Tang, Huairong
Sun, Ronghao
Li, Chao
Bai, Bing
Jia, Weiguo
Liu, Yi
Zhang, Wei
Yang, Li
Peng, Yong
Dai, Lunzhi
Hu, Hongbo
Jiang, Yong
Hu, Yiguo
Zhu, Jingqiang
Jiang, Hong
Li, Zhihui
Caulin, Carlos
Park, Jihwan
Xu, Heng
author_sort Luo, Han
collection PubMed
description Cancer-associated fibroblasts (CAFs) are the predominant components of the tumor microenvironment (TME) and influence cancer hallmarks, but without systematic investigation on their ubiquitous characteristics across different cancer types. Here, we perform pan-cancer analysis on 226 samples across 10 solid cancer types to profile the TME at single-cell resolution, illustrating the commonalities/plasticity of heterogenous CAFs. Activation trajectory of the major CAF types is divided into three states, exhibiting distinct interactions with other cell components, and relating to prognosis of immunotherapy. Moreover, minor CAF components represent the alternative origin from other TME components (e.g., endothelia and macrophages). Particularly, the ubiquitous presentation of endothelial-to-mesenchymal transition CAF, which may interact with proximal SPP1(+) tumor-associated macrophages, is implicated in endothelial-to-mesenchymal transition and survival stratifications. Our study comprehensively profiles the shared characteristics and dynamics of CAFs, and highlight their heterogeneity and plasticity across different cancer types. Browser of integrated pan-cancer single-cell information is available at https://gist-fgl.github.io/sc-caf-atlas/.
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spelling pubmed-96364082022-11-06 Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment Luo, Han Xia, Xuyang Huang, Li-Bin An, Hyunsu Cao, Minyuan Kim, Gyeong Dae Chen, Hai-Ning Zhang, Wei-Han Shu, Yang Kong, Xiangyu Ren, Zhixiang Li, Pei-Heng Liu, Yang Tang, Huairong Sun, Ronghao Li, Chao Bai, Bing Jia, Weiguo Liu, Yi Zhang, Wei Yang, Li Peng, Yong Dai, Lunzhi Hu, Hongbo Jiang, Yong Hu, Yiguo Zhu, Jingqiang Jiang, Hong Li, Zhihui Caulin, Carlos Park, Jihwan Xu, Heng Nat Commun Article Cancer-associated fibroblasts (CAFs) are the predominant components of the tumor microenvironment (TME) and influence cancer hallmarks, but without systematic investigation on their ubiquitous characteristics across different cancer types. Here, we perform pan-cancer analysis on 226 samples across 10 solid cancer types to profile the TME at single-cell resolution, illustrating the commonalities/plasticity of heterogenous CAFs. Activation trajectory of the major CAF types is divided into three states, exhibiting distinct interactions with other cell components, and relating to prognosis of immunotherapy. Moreover, minor CAF components represent the alternative origin from other TME components (e.g., endothelia and macrophages). Particularly, the ubiquitous presentation of endothelial-to-mesenchymal transition CAF, which may interact with proximal SPP1(+) tumor-associated macrophages, is implicated in endothelial-to-mesenchymal transition and survival stratifications. Our study comprehensively profiles the shared characteristics and dynamics of CAFs, and highlight their heterogeneity and plasticity across different cancer types. Browser of integrated pan-cancer single-cell information is available at https://gist-fgl.github.io/sc-caf-atlas/. Nature Publishing Group UK 2022-11-04 /pmc/articles/PMC9636408/ /pubmed/36333338 http://dx.doi.org/10.1038/s41467-022-34395-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Luo, Han
Xia, Xuyang
Huang, Li-Bin
An, Hyunsu
Cao, Minyuan
Kim, Gyeong Dae
Chen, Hai-Ning
Zhang, Wei-Han
Shu, Yang
Kong, Xiangyu
Ren, Zhixiang
Li, Pei-Heng
Liu, Yang
Tang, Huairong
Sun, Ronghao
Li, Chao
Bai, Bing
Jia, Weiguo
Liu, Yi
Zhang, Wei
Yang, Li
Peng, Yong
Dai, Lunzhi
Hu, Hongbo
Jiang, Yong
Hu, Yiguo
Zhu, Jingqiang
Jiang, Hong
Li, Zhihui
Caulin, Carlos
Park, Jihwan
Xu, Heng
Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
title Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
title_full Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
title_fullStr Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
title_full_unstemmed Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
title_short Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
title_sort pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636408/
https://www.ncbi.nlm.nih.gov/pubmed/36333338
http://dx.doi.org/10.1038/s41467-022-34395-2
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