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Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma
BACKGROUND: Sorafenib is a multi-kinase inhibitor that shows antitumor activity in advanced hepatocellular carcinoma. Sorafenib exerts a regulatory effect on immune cells, including T cells, natural killer cells and dendritic cells. Studies have shown that plasmacytoid dendritic cells (pDCs) are fun...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710007/ https://www.ncbi.nlm.nih.gov/pubmed/36451110 http://dx.doi.org/10.1186/s12885-022-10356-2 |
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author | Zhang, Xinning Xu, Yong Zhao, Guodong Liu, Rong Yu, Haisheng |
author_facet | Zhang, Xinning Xu, Yong Zhao, Guodong Liu, Rong Yu, Haisheng |
author_sort | Zhang, Xinning |
collection | PubMed |
description | BACKGROUND: Sorafenib is a multi-kinase inhibitor that shows antitumor activity in advanced hepatocellular carcinoma. Sorafenib exerts a regulatory effect on immune cells, including T cells, natural killer cells and dendritic cells. Studies have shown that plasmacytoid dendritic cells (pDCs) are functionally impaired in cancer tissues or produce low type I interferon alpha (IFNα) in cancer microenvironments. However, the effects of sorafenib on the function of pDCs have not been evaluated in detail. METHODS: Normal and patient PBMCs were stimulated with CpG-A to evaluate IFNα production with Flow cytometry and ELISA. RESULT: We analyzed the production of IFNα by PBMCs in patients with advanced HCC under sorafenib treatment. We found that sorafenib-treated HCC patients produced less IFNα than untreated patients. Furthermore, we demonstrated that sorafenib suppressed the production of IFNα by PBMCs or pDCs from heathy donors in a concentration-dependent manner. CONCLUSION: Sorafenib suppressed pDCs function. Given that sorafenib is a currently recommended targeted therapeutic agent against cancer, our results suggest that its immunosuppressive effect on pDCs should be considered during treatment. |
format | Online Article Text |
id | pubmed-9710007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97100072022-12-01 Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma Zhang, Xinning Xu, Yong Zhao, Guodong Liu, Rong Yu, Haisheng BMC Cancer Research Article BACKGROUND: Sorafenib is a multi-kinase inhibitor that shows antitumor activity in advanced hepatocellular carcinoma. Sorafenib exerts a regulatory effect on immune cells, including T cells, natural killer cells and dendritic cells. Studies have shown that plasmacytoid dendritic cells (pDCs) are functionally impaired in cancer tissues or produce low type I interferon alpha (IFNα) in cancer microenvironments. However, the effects of sorafenib on the function of pDCs have not been evaluated in detail. METHODS: Normal and patient PBMCs were stimulated with CpG-A to evaluate IFNα production with Flow cytometry and ELISA. RESULT: We analyzed the production of IFNα by PBMCs in patients with advanced HCC under sorafenib treatment. We found that sorafenib-treated HCC patients produced less IFNα than untreated patients. Furthermore, we demonstrated that sorafenib suppressed the production of IFNα by PBMCs or pDCs from heathy donors in a concentration-dependent manner. CONCLUSION: Sorafenib suppressed pDCs function. Given that sorafenib is a currently recommended targeted therapeutic agent against cancer, our results suggest that its immunosuppressive effect on pDCs should be considered during treatment. BioMed Central 2022-11-30 /pmc/articles/PMC9710007/ /pubmed/36451110 http://dx.doi.org/10.1186/s12885-022-10356-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Zhang, Xinning Xu, Yong Zhao, Guodong Liu, Rong Yu, Haisheng Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
title | Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
title_full | Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
title_fullStr | Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
title_full_unstemmed | Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
title_short | Sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
title_sort | sorafenib inhibits interferon production by plasmacytoid dendritic cells in hepatocellular carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710007/ https://www.ncbi.nlm.nih.gov/pubmed/36451110 http://dx.doi.org/10.1186/s12885-022-10356-2 |
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