Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783572822692462592 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7438587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhangjiahui tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT jicheng tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT liwei tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT maozheying tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT shiyinghong tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT shihui tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT jirunbi tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT qianhui tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT xuwenrong tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis AT zhangxu tumoreducatedneutrophilsactivatemesenchymalstemcellstopromotegastriccancergrowthandmetastasis |