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Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis

In response to tumor signals, mesenchymal stem cells (MSCs) are recruited to tumor sites and activated to promote tumor progression. Emerging evidences suggest that in addition to tumor cells, non-tumor cells in tumor microenvironment could also interact with MSCs to regulate their phenotype and fun...

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Autores principales: Zhang, Jiahui, Ji, Cheng, Li, Wei, Mao, Zheying, Shi, Yinghong, Shi, Hui, Ji, Runbi, Qian, Hui, Xu, Wenrong, Zhang, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438587/
https://www.ncbi.nlm.nih.gov/pubmed/32903528
http://dx.doi.org/10.3389/fcell.2020.00788
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author Zhang, Jiahui
Ji, Cheng
Li, Wei
Mao, Zheying
Shi, Yinghong
Shi, Hui
Ji, Runbi
Qian, Hui
Xu, Wenrong
Zhang, Xu
author_facet Zhang, Jiahui
Ji, Cheng
Li, Wei
Mao, Zheying
Shi, Yinghong
Shi, Hui
Ji, Runbi
Qian, Hui
Xu, Wenrong
Zhang, Xu
author_sort Zhang, Jiahui
collection PubMed
description In response to tumor signals, mesenchymal stem cells (MSCs) are recruited to tumor sites and activated to promote tumor progression. Emerging evidences suggest that in addition to tumor cells, non-tumor cells in tumor microenvironment could also interact with MSCs to regulate their phenotype and function. However, the mechanism for MSCs regulation in gastric cancer has not been fully understood. In this study, we reported that tumor-educated neutrophils (TENs) induced the transformation of MSCs into cancer-associated fibroblasts (CAFs) which in turn remarkably facilitated gastric cancer growth and metastasis. Mechanistic study showed that TENs exerted their effects by secreting inflammatory factors including IL-17, IL-23 and TNF-α, which triggered the activation of AKT and p38 pathways in MSCs. Pre-treatment with neutralizing antibodies to these inflammatory factors or pathway inhibitors reversed TENs-induced transformation of MSCs to CAFs. Taken together, these data suggest that TENs promote gastric cancer progression through the regulation of MSCs/CAFs transformation.
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spelling pubmed-74385872020-09-03 Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis Zhang, Jiahui Ji, Cheng Li, Wei Mao, Zheying Shi, Yinghong Shi, Hui Ji, Runbi Qian, Hui Xu, Wenrong Zhang, Xu Front Cell Dev Biol Cell and Developmental Biology In response to tumor signals, mesenchymal stem cells (MSCs) are recruited to tumor sites and activated to promote tumor progression. Emerging evidences suggest that in addition to tumor cells, non-tumor cells in tumor microenvironment could also interact with MSCs to regulate their phenotype and function. However, the mechanism for MSCs regulation in gastric cancer has not been fully understood. In this study, we reported that tumor-educated neutrophils (TENs) induced the transformation of MSCs into cancer-associated fibroblasts (CAFs) which in turn remarkably facilitated gastric cancer growth and metastasis. Mechanistic study showed that TENs exerted their effects by secreting inflammatory factors including IL-17, IL-23 and TNF-α, which triggered the activation of AKT and p38 pathways in MSCs. Pre-treatment with neutralizing antibodies to these inflammatory factors or pathway inhibitors reversed TENs-induced transformation of MSCs to CAFs. Taken together, these data suggest that TENs promote gastric cancer progression through the regulation of MSCs/CAFs transformation. Frontiers Media S.A. 2020-08-13 /pmc/articles/PMC7438587/ /pubmed/32903528 http://dx.doi.org/10.3389/fcell.2020.00788 Text en Copyright © 2020 Zhang, Ji, Li, Mao, Shi, Shi, Ji, Qian, Xu and Zhang. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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 Cell and Developmental Biology
Zhang, Jiahui
Ji, Cheng
Li, Wei
Mao, Zheying
Shi, Yinghong
Shi, Hui
Ji, Runbi
Qian, Hui
Xu, Wenrong
Zhang, Xu
Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis
title Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis
title_full Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis
title_fullStr Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis
title_full_unstemmed Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis
title_short Tumor-Educated Neutrophils Activate Mesenchymal Stem Cells to Promote Gastric Cancer Growth and Metastasis
title_sort tumor-educated neutrophils activate mesenchymal stem cells to promote gastric cancer growth and metastasis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438587/
https://www.ncbi.nlm.nih.gov/pubmed/32903528
http://dx.doi.org/10.3389/fcell.2020.00788
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