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Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts

Cancer-associated fibroblasts (CAFs), one of the major components of a tumour microenvironment, comprise heterogeneous populations involved in tumour progression. However, it remains obscure how CAF heterogeneity is governed by cancer cells. Here, we show that cancer extracellular vesicles (EVs) ind...

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Autores principales: Naito, Yutaka, Yamamoto, Yusuke, Sakamoto, Naoya, Shimomura, Iwao, Kogure, Akiko, Kumazaki, Minami, Yokoi, Akira, Yashiro, Masakazu, Kiyono, Tohru, Yanagihara, Kazuyoshi, Takahashi, Ryou-u, Hirakawa, Kosei, Yasui, Wataru, Ochiya, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755971/
https://www.ncbi.nlm.nih.gov/pubmed/31147602
http://dx.doi.org/10.1038/s41388-019-0832-4
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author Naito, Yutaka
Yamamoto, Yusuke
Sakamoto, Naoya
Shimomura, Iwao
Kogure, Akiko
Kumazaki, Minami
Yokoi, Akira
Yashiro, Masakazu
Kiyono, Tohru
Yanagihara, Kazuyoshi
Takahashi, Ryou-u
Hirakawa, Kosei
Yasui, Wataru
Ochiya, Takahiro
author_facet Naito, Yutaka
Yamamoto, Yusuke
Sakamoto, Naoya
Shimomura, Iwao
Kogure, Akiko
Kumazaki, Minami
Yokoi, Akira
Yashiro, Masakazu
Kiyono, Tohru
Yanagihara, Kazuyoshi
Takahashi, Ryou-u
Hirakawa, Kosei
Yasui, Wataru
Ochiya, Takahiro
author_sort Naito, Yutaka
collection PubMed
description Cancer-associated fibroblasts (CAFs), one of the major components of a tumour microenvironment, comprise heterogeneous populations involved in tumour progression. However, it remains obscure how CAF heterogeneity is governed by cancer cells. Here, we show that cancer extracellular vesicles (EVs) induce a series of chemokines in activated fibroblasts and contribute to the formation of the heterogeneity. In a xenograft model of diffuse-type gastric cancer, we showed two distinct fibroblast subpopulations with alpha-smooth muscle actin (α-SMA) expression or chemokine expression. MicroRNAs (miRNAs) profiling of the EVs and the transfection experiment suggested that several miRNAs played a role in the induction of chemokines such as CXCL1 and CXCL8 in fibroblasts, but not for the myofibroblastic differentiation. Clinically, aberrant activation of CXCL1 and CXCL8 in CAFs correlated with poorer survival in gastric cancer patients. Thus, this link between chemokine expression in CAFs and tumour progression may provide novel targets for anticancer therapy.
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spelling pubmed-67559712019-09-24 Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts Naito, Yutaka Yamamoto, Yusuke Sakamoto, Naoya Shimomura, Iwao Kogure, Akiko Kumazaki, Minami Yokoi, Akira Yashiro, Masakazu Kiyono, Tohru Yanagihara, Kazuyoshi Takahashi, Ryou-u Hirakawa, Kosei Yasui, Wataru Ochiya, Takahiro Oncogene Article Cancer-associated fibroblasts (CAFs), one of the major components of a tumour microenvironment, comprise heterogeneous populations involved in tumour progression. However, it remains obscure how CAF heterogeneity is governed by cancer cells. Here, we show that cancer extracellular vesicles (EVs) induce a series of chemokines in activated fibroblasts and contribute to the formation of the heterogeneity. In a xenograft model of diffuse-type gastric cancer, we showed two distinct fibroblast subpopulations with alpha-smooth muscle actin (α-SMA) expression or chemokine expression. MicroRNAs (miRNAs) profiling of the EVs and the transfection experiment suggested that several miRNAs played a role in the induction of chemokines such as CXCL1 and CXCL8 in fibroblasts, but not for the myofibroblastic differentiation. Clinically, aberrant activation of CXCL1 and CXCL8 in CAFs correlated with poorer survival in gastric cancer patients. Thus, this link between chemokine expression in CAFs and tumour progression may provide novel targets for anticancer therapy. Nature Publishing Group UK 2019-05-30 2019 /pmc/articles/PMC6755971/ /pubmed/31147602 http://dx.doi.org/10.1038/s41388-019-0832-4 Text en © The Author(s) 2019 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/.
spellingShingle Article
Naito, Yutaka
Yamamoto, Yusuke
Sakamoto, Naoya
Shimomura, Iwao
Kogure, Akiko
Kumazaki, Minami
Yokoi, Akira
Yashiro, Masakazu
Kiyono, Tohru
Yanagihara, Kazuyoshi
Takahashi, Ryou-u
Hirakawa, Kosei
Yasui, Wataru
Ochiya, Takahiro
Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
title Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
title_full Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
title_fullStr Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
title_full_unstemmed Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
title_short Cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
title_sort cancer extracellular vesicles contribute to stromal heterogeneity by inducing chemokines in cancer-associated fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755971/
https://www.ncbi.nlm.nih.gov/pubmed/31147602
http://dx.doi.org/10.1038/s41388-019-0832-4
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