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CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions
CXC chemokine ligand‐10 (CXCL10) is a small (10 kDa) secretory protein in the CXC subfamily of cytokines. CXCL10 has been reported to play an important role in antitumor immunity as a chemotactic factor. Tumor development is always accompanied by the formation of an immunosuppressive tumor microenvi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807505/ https://www.ncbi.nlm.nih.gov/pubmed/36168841 http://dx.doi.org/10.1111/cas.15598 |
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author | Sun, Yingying Mo, Yan Jiang, Shu Shang, Chao Feng, Yunpeng Zeng, Xianlu |
author_facet | Sun, Yingying Mo, Yan Jiang, Shu Shang, Chao Feng, Yunpeng Zeng, Xianlu |
author_sort | Sun, Yingying |
collection | PubMed |
description | CXC chemokine ligand‐10 (CXCL10) is a small (10 kDa) secretory protein in the CXC subfamily of cytokines. CXCL10 has been reported to play an important role in antitumor immunity as a chemotactic factor. Tumor development is always accompanied by the formation of an immunosuppressive tumor microenvironment, and the role of CXCL10 in tumor immunosuppression remains unclear. Here, we reported that CXCL10 expression was significantly upregulated in mice with melanoma, and tumor cells secreted large amounts of CXCL10. Myeloid‐derived suppressor cells (MDSCs) are an important part of the immunosuppressive tumor microenvironment. Our results showed that CXCL10 promoted the proliferation of monocyte‐like (mo)‐MDSCs by activating the p38 MAPK signaling pathway through CXCR3, which led to the abnormal accumulation of mo‐MDSCs under tumor conditions. This finding provides a new understanding of the mechanism by which a tumor‐induced immunosuppressive microenvironment forms and suggests that CXCL10 could be a potential intervention target for slowing tumor progression. |
format | Online Article Text |
id | pubmed-9807505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98075052023-01-04 CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions Sun, Yingying Mo, Yan Jiang, Shu Shang, Chao Feng, Yunpeng Zeng, Xianlu Cancer Sci Original Articles CXC chemokine ligand‐10 (CXCL10) is a small (10 kDa) secretory protein in the CXC subfamily of cytokines. CXCL10 has been reported to play an important role in antitumor immunity as a chemotactic factor. Tumor development is always accompanied by the formation of an immunosuppressive tumor microenvironment, and the role of CXCL10 in tumor immunosuppression remains unclear. Here, we reported that CXCL10 expression was significantly upregulated in mice with melanoma, and tumor cells secreted large amounts of CXCL10. Myeloid‐derived suppressor cells (MDSCs) are an important part of the immunosuppressive tumor microenvironment. Our results showed that CXCL10 promoted the proliferation of monocyte‐like (mo)‐MDSCs by activating the p38 MAPK signaling pathway through CXCR3, which led to the abnormal accumulation of mo‐MDSCs under tumor conditions. This finding provides a new understanding of the mechanism by which a tumor‐induced immunosuppressive microenvironment forms and suggests that CXCL10 could be a potential intervention target for slowing tumor progression. John Wiley and Sons Inc. 2022-11-03 /pmc/articles/PMC9807505/ /pubmed/36168841 http://dx.doi.org/10.1111/cas.15598 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Sun, Yingying Mo, Yan Jiang, Shu Shang, Chao Feng, Yunpeng Zeng, Xianlu CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions |
title |
CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions |
title_full |
CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions |
title_fullStr |
CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions |
title_full_unstemmed |
CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions |
title_short |
CXC chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 MAPK signaling under tumor conditions |
title_sort | cxc chemokine ligand‐10 promotes the accumulation of monocyte‐like myeloid‐derived suppressor cells by activating p38 mapk signaling under tumor conditions |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807505/ https://www.ncbi.nlm.nih.gov/pubmed/36168841 http://dx.doi.org/10.1111/cas.15598 |
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