Cargando…
Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6
In breast cancer, the most numerous stromal cells are cancer-associated fibroblasts (CAFs), which are associated with disease progression and chemoresistance. However, few studies have explored the function of CAFs in breast cancer cell radiosensitivity. Here, CAF-derived conditioned media was obser...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837084/ https://www.ncbi.nlm.nih.gov/pubmed/36635302 http://dx.doi.org/10.1038/s41420-023-01306-3 |
_version_ | 1784868997897912320 |
---|---|
author | Guo, Zhaoze Zhang, Han Fu, Yiming Kuang, Junjie Zhao, Bei Zhang, LanFang Lin, Jie Lin, Shuhui Wu, Dehua Xie, Guozhu |
author_facet | Guo, Zhaoze Zhang, Han Fu, Yiming Kuang, Junjie Zhao, Bei Zhang, LanFang Lin, Jie Lin, Shuhui Wu, Dehua Xie, Guozhu |
author_sort | Guo, Zhaoze |
collection | PubMed |
description | In breast cancer, the most numerous stromal cells are cancer-associated fibroblasts (CAFs), which are associated with disease progression and chemoresistance. However, few studies have explored the function of CAFs in breast cancer cell radiosensitivity. Here, CAF-derived conditioned media was observed to induce breast cancer cell growth and radioresistance. CAFs secrete interleukin 6 (IL-6) which activates signal transducer and activator of transcription 3 (STAT3) signaling pathway, thus promoting the growth and radioresistance of breast cancer cells. Treatment with an inhibitor of STAT3 or an IL-6 neutralizing antibody blocked the growth and radioresistance induced by CAFs. In in vivo mouse models, tocilizumab (an IL-6 receptor monoclonal antibody) abrogated CAF-induced growth and radioresistance. Moreover, in breast cancer, a poor response to radiotherapy was associated with IL-6 and p-STAT3 expression. These results indicated that IL-6 mediates cross-talk between breast cancer cells and CAFs in the tumor microenvironment. Our results identified the IL-6/STAT3 signaling pathway as an important therapeutic target in breast cancer radiotherapy. |
format | Online Article Text |
id | pubmed-9837084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98370842023-01-14 Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 Guo, Zhaoze Zhang, Han Fu, Yiming Kuang, Junjie Zhao, Bei Zhang, LanFang Lin, Jie Lin, Shuhui Wu, Dehua Xie, Guozhu Cell Death Discov Article In breast cancer, the most numerous stromal cells are cancer-associated fibroblasts (CAFs), which are associated with disease progression and chemoresistance. However, few studies have explored the function of CAFs in breast cancer cell radiosensitivity. Here, CAF-derived conditioned media was observed to induce breast cancer cell growth and radioresistance. CAFs secrete interleukin 6 (IL-6) which activates signal transducer and activator of transcription 3 (STAT3) signaling pathway, thus promoting the growth and radioresistance of breast cancer cells. Treatment with an inhibitor of STAT3 or an IL-6 neutralizing antibody blocked the growth and radioresistance induced by CAFs. In in vivo mouse models, tocilizumab (an IL-6 receptor monoclonal antibody) abrogated CAF-induced growth and radioresistance. Moreover, in breast cancer, a poor response to radiotherapy was associated with IL-6 and p-STAT3 expression. These results indicated that IL-6 mediates cross-talk between breast cancer cells and CAFs in the tumor microenvironment. Our results identified the IL-6/STAT3 signaling pathway as an important therapeutic target in breast cancer radiotherapy. Nature Publishing Group UK 2023-01-13 /pmc/articles/PMC9837084/ /pubmed/36635302 http://dx.doi.org/10.1038/s41420-023-01306-3 Text en © The Author(s) 2023 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 Guo, Zhaoze Zhang, Han Fu, Yiming Kuang, Junjie Zhao, Bei Zhang, LanFang Lin, Jie Lin, Shuhui Wu, Dehua Xie, Guozhu Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 |
title | Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 |
title_full | Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 |
title_fullStr | Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 |
title_full_unstemmed | Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 |
title_short | Cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine IL-6 |
title_sort | cancer-associated fibroblasts induce growth and radioresistance of breast cancer cells through paracrine il-6 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837084/ https://www.ncbi.nlm.nih.gov/pubmed/36635302 http://dx.doi.org/10.1038/s41420-023-01306-3 |
work_keys_str_mv | AT guozhaoze cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT zhanghan cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT fuyiming cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT kuangjunjie cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT zhaobei cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT zhanglanfang cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT linjie cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT linshuhui cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT wudehua cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 AT xieguozhu cancerassociatedfibroblastsinducegrowthandradioresistanceofbreastcancercellsthroughparacrineil6 |