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Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer
BACKGROUND: The roles of different subtypes of tumour‐associated macrophages (TAMs) in predicting the prognosis of colorectal cancer (CRC) remain controversial. In this study, different subtypes of TAMs were investigated as prognostic and predictive biomarkers for CRC. METHODS: Expressions of CD68,...
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/PMC9286461/ https://www.ncbi.nlm.nih.gov/pubmed/34964155 http://dx.doi.org/10.1111/sji.13137 |
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author | Kou, Yu Li, Zhuoqun Sun, Qidi Yang, Shengnan Wang, Yunshuai Hu, Chen Gu, Huijie Wang, Huangjian Xu, Hairong Li, Yan Han, Baowei |
author_facet | Kou, Yu Li, Zhuoqun Sun, Qidi Yang, Shengnan Wang, Yunshuai Hu, Chen Gu, Huijie Wang, Huangjian Xu, Hairong Li, Yan Han, Baowei |
author_sort | Kou, Yu |
collection | PubMed |
description | BACKGROUND: The roles of different subtypes of tumour‐associated macrophages (TAMs) in predicting the prognosis of colorectal cancer (CRC) remain controversial. In this study, different subtypes of TAMs were investigated as prognostic and predictive biomarkers for CRC. METHODS: Expressions of CD68, CD86 and CD163 were investigated by immunohistochemistry (IHC) and immunofluorescence (IF), and the correlation between the expression of CD86 and CD163 was calculated in colorectal cancer tissues from 64 CRC patients. RESULTS: The results showed that high expressions of CD86(+) and CD68(+)CD86(+) TAMs as well as low expression of CD163(+) and CD68(+)CD163(+) TAMs were significantly associated with favourable overall survival (OS). The level of CD86 protein expression showed a negative correlation with CD163 protein expression. In addition, CD86 protein expression remarkably negatively correlated with tumour differentiation and tumour node metastasis (TNM) stage, while CD163 protein expression significantly positively correlated with tumour differentiation and tumour size. As an independent risk factor, high expression of CD86 TAMs had prominently favourable prognostic efficacy, while high expression of CD68(+)CD163(+) TAMs had significantly poor prognostic efficacy. CONCLUSIONS: These results indicate that CD86(+) and CD68(+)CD163(+) TAMs as prognostic and predictive biomarkers for CRC. |
format | Online Article Text |
id | pubmed-9286461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92864612022-07-19 Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer Kou, Yu Li, Zhuoqun Sun, Qidi Yang, Shengnan Wang, Yunshuai Hu, Chen Gu, Huijie Wang, Huangjian Xu, Hairong Li, Yan Han, Baowei Scand J Immunol Original Articles BACKGROUND: The roles of different subtypes of tumour‐associated macrophages (TAMs) in predicting the prognosis of colorectal cancer (CRC) remain controversial. In this study, different subtypes of TAMs were investigated as prognostic and predictive biomarkers for CRC. METHODS: Expressions of CD68, CD86 and CD163 were investigated by immunohistochemistry (IHC) and immunofluorescence (IF), and the correlation between the expression of CD86 and CD163 was calculated in colorectal cancer tissues from 64 CRC patients. RESULTS: The results showed that high expressions of CD86(+) and CD68(+)CD86(+) TAMs as well as low expression of CD163(+) and CD68(+)CD163(+) TAMs were significantly associated with favourable overall survival (OS). The level of CD86 protein expression showed a negative correlation with CD163 protein expression. In addition, CD86 protein expression remarkably negatively correlated with tumour differentiation and tumour node metastasis (TNM) stage, while CD163 protein expression significantly positively correlated with tumour differentiation and tumour size. As an independent risk factor, high expression of CD86 TAMs had prominently favourable prognostic efficacy, while high expression of CD68(+)CD163(+) TAMs had significantly poor prognostic efficacy. CONCLUSIONS: These results indicate that CD86(+) and CD68(+)CD163(+) TAMs as prognostic and predictive biomarkers for CRC. John Wiley and Sons Inc. 2022-01-10 2022-04 /pmc/articles/PMC9286461/ /pubmed/34964155 http://dx.doi.org/10.1111/sji.13137 Text en © 2021 The Authors. Scandinavian Journal of Immunology published by John Wiley & Sons Ltd on behalf of The Scandinavian Foundation for Immunology https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kou, Yu Li, Zhuoqun Sun, Qidi Yang, Shengnan Wang, Yunshuai Hu, Chen Gu, Huijie Wang, Huangjian Xu, Hairong Li, Yan Han, Baowei Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
title | Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
title_full | Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
title_fullStr | Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
title_full_unstemmed | Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
title_short | Prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
title_sort | prognostic value and predictive biomarkers of phenotypes of tumour‐associated macrophages in colorectal cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286461/ https://www.ncbi.nlm.nih.gov/pubmed/34964155 http://dx.doi.org/10.1111/sji.13137 |
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