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Tumor-associated macrophages in lung cancer: Friend or foe?
Typically, tumor-associated macrophages (TAMs), an abundant population of leukocytes in lung cancer, are affected by tumor microenvironment (TME) and shift towards either a pro-tumor (M2-like) or an anti-tumor phenotype (M1-like). M2-polarized macrophages, are one of the primary tumor-infiltrating i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533506/ https://www.ncbi.nlm.nih.gov/pubmed/33000214 http://dx.doi.org/10.3892/mmr.2020.11518 |
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author | Xu, Fei Wei, Ying Tang, Zhao Liu, Baojun Dong, Jingcheng |
author_facet | Xu, Fei Wei, Ying Tang, Zhao Liu, Baojun Dong, Jingcheng |
author_sort | Xu, Fei |
collection | PubMed |
description | Typically, tumor-associated macrophages (TAMs), an abundant population of leukocytes in lung cancer, are affected by tumor microenvironment (TME) and shift towards either a pro-tumor (M2-like) or an anti-tumor phenotype (M1-like). M2-polarized macrophages, are one of the primary tumor-infiltrating immune cells and were reported to be associated with the promotion of cancer cell growth, invasion, metastasis, and angiogenesis. TAMs are considered a potential target for adjuvant anticancer therapies, and recent therapeutic approaches targeting the M2 polarization of TAMs have shown encouraging results. The present review discusses recent developments in the role of TAMs in cancer, in particular TAMs functions, clinical implication and prospective therapeutic strategies in lung cancer. |
format | Online Article Text |
id | pubmed-7533506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-75335062020-10-07 Tumor-associated macrophages in lung cancer: Friend or foe? Xu, Fei Wei, Ying Tang, Zhao Liu, Baojun Dong, Jingcheng Mol Med Rep Review Typically, tumor-associated macrophages (TAMs), an abundant population of leukocytes in lung cancer, are affected by tumor microenvironment (TME) and shift towards either a pro-tumor (M2-like) or an anti-tumor phenotype (M1-like). M2-polarized macrophages, are one of the primary tumor-infiltrating immune cells and were reported to be associated with the promotion of cancer cell growth, invasion, metastasis, and angiogenesis. TAMs are considered a potential target for adjuvant anticancer therapies, and recent therapeutic approaches targeting the M2 polarization of TAMs have shown encouraging results. The present review discusses recent developments in the role of TAMs in cancer, in particular TAMs functions, clinical implication and prospective therapeutic strategies in lung cancer. D.A. Spandidos 2020-11 2020-09-17 /pmc/articles/PMC7533506/ /pubmed/33000214 http://dx.doi.org/10.3892/mmr.2020.11518 Text en Copyright: © Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 | Review Xu, Fei Wei, Ying Tang, Zhao Liu, Baojun Dong, Jingcheng Tumor-associated macrophages in lung cancer: Friend or foe? |
title | Tumor-associated macrophages in lung cancer: Friend or foe? |
title_full | Tumor-associated macrophages in lung cancer: Friend or foe? |
title_fullStr | Tumor-associated macrophages in lung cancer: Friend or foe? |
title_full_unstemmed | Tumor-associated macrophages in lung cancer: Friend or foe? |
title_short | Tumor-associated macrophages in lung cancer: Friend or foe? |
title_sort | tumor-associated macrophages in lung cancer: friend or foe? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533506/ https://www.ncbi.nlm.nih.gov/pubmed/33000214 http://dx.doi.org/10.3892/mmr.2020.11518 |
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