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Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy
Hepatocellular carcinoma (HCC), one of the most malignant tumors, is characterized by its stubborn immunosuppressive microenvironment. As one of the main members of the tumor microenvironment (TME) of HCC, tumor-associated macrophages (TAMs) play a critical role in its occurrence and development, in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931715/ https://www.ncbi.nlm.nih.gov/pubmed/36792608 http://dx.doi.org/10.1038/s41420-023-01356-7 |
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author | Zheng, Hongyu Peng, Xueqiang Yang, Shuo Li, Xinyu Huang, Mingyao Wei, Shibo Zhang, Sheng He, Guangpeng Liu, Jiaxing Fan, Qing Yang, Liang Li, Hangyu |
author_facet | Zheng, Hongyu Peng, Xueqiang Yang, Shuo Li, Xinyu Huang, Mingyao Wei, Shibo Zhang, Sheng He, Guangpeng Liu, Jiaxing Fan, Qing Yang, Liang Li, Hangyu |
author_sort | Zheng, Hongyu |
collection | PubMed |
description | Hepatocellular carcinoma (HCC), one of the most malignant tumors, is characterized by its stubborn immunosuppressive microenvironment. As one of the main members of the tumor microenvironment (TME) of HCC, tumor-associated macrophages (TAMs) play a critical role in its occurrence and development, including stimulating angiogenesis, enhancing immunosuppression, and promoting the drug resistance and cancer metastasis. This review describes the origin as well as phenotypic heterogeneity of TAMs and their potential effects on the occurrence and development of HCC and also discusses about various adjuvant therapy based strategies that can be used for targeting TAMs. In addition, we have highlighted different treatment modalities for TAMs based on immunotherapy, including small molecular inhibitors, immune checkpoint inhibitors, antibodies, tumor vaccines, adoptive cellular immunotherapy, and nanocarriers for drug delivery, to explore novel combination therapies and provide feasible therapeutic options for clinically improving the prognosis and quality of life of HCC patients. |
format | Online Article Text |
id | pubmed-9931715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99317152023-02-17 Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy Zheng, Hongyu Peng, Xueqiang Yang, Shuo Li, Xinyu Huang, Mingyao Wei, Shibo Zhang, Sheng He, Guangpeng Liu, Jiaxing Fan, Qing Yang, Liang Li, Hangyu Cell Death Discov Review Article Hepatocellular carcinoma (HCC), one of the most malignant tumors, is characterized by its stubborn immunosuppressive microenvironment. As one of the main members of the tumor microenvironment (TME) of HCC, tumor-associated macrophages (TAMs) play a critical role in its occurrence and development, including stimulating angiogenesis, enhancing immunosuppression, and promoting the drug resistance and cancer metastasis. This review describes the origin as well as phenotypic heterogeneity of TAMs and their potential effects on the occurrence and development of HCC and also discusses about various adjuvant therapy based strategies that can be used for targeting TAMs. In addition, we have highlighted different treatment modalities for TAMs based on immunotherapy, including small molecular inhibitors, immune checkpoint inhibitors, antibodies, tumor vaccines, adoptive cellular immunotherapy, and nanocarriers for drug delivery, to explore novel combination therapies and provide feasible therapeutic options for clinically improving the prognosis and quality of life of HCC patients. Nature Publishing Group UK 2023-02-15 /pmc/articles/PMC9931715/ /pubmed/36792608 http://dx.doi.org/10.1038/s41420-023-01356-7 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 | Review Article Zheng, Hongyu Peng, Xueqiang Yang, Shuo Li, Xinyu Huang, Mingyao Wei, Shibo Zhang, Sheng He, Guangpeng Liu, Jiaxing Fan, Qing Yang, Liang Li, Hangyu Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
title | Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
title_full | Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
title_fullStr | Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
title_full_unstemmed | Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
title_short | Targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
title_sort | targeting tumor-associated macrophages in hepatocellular carcinoma: biology, strategy, and immunotherapy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931715/ https://www.ncbi.nlm.nih.gov/pubmed/36792608 http://dx.doi.org/10.1038/s41420-023-01356-7 |
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