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Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer

BACKGROUND: The microsatellite instability (MSI) in colorectal cancer (CRC) has a more favorable clinical outcome and is characterized by highly upregulated expression of various immunological checkpoints than microsatellite stable (MSS) tumors. Apoptosis inhibitor of macrophage (AIM) is a circulati...

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Autores principales: Huang, Wen-juan, Wang, Xin, Zhang, Meng-lin, Li, Li, Wang, Rui-tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654032/
https://www.ncbi.nlm.nih.gov/pubmed/33172404
http://dx.doi.org/10.1186/s12876-020-01520-8
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author Huang, Wen-juan
Wang, Xin
Zhang, Meng-lin
Li, Li
Wang, Rui-tao
author_facet Huang, Wen-juan
Wang, Xin
Zhang, Meng-lin
Li, Li
Wang, Rui-tao
author_sort Huang, Wen-juan
collection PubMed
description BACKGROUND: The microsatellite instability (MSI) in colorectal cancer (CRC) has a more favorable clinical outcome and is characterized by highly upregulated expression of various immunological checkpoints than microsatellite stable (MSS) tumors. Apoptosis inhibitor of macrophage (AIM) is a circulating protein and circulates throughout the body to remove cellular debris. The aim of this study was to evaluate the association between MSI status and AIM levels in CRC patients. METHODS: In this study, we evaluated the levels of AIM by Enzyme Linked Immuno-Sorbent Assay (ELISA) in serum of 430 CRC patients. All patients’ clinical and laboratory characteristics at initial diagnosis were collected. The relationship between AIM levels and MSI status was examined. RESULTS: 64 patients (14.9%) were identified as having MSI-H (high-frequency MSI) and 366 casess (85.1%) having MSS. Patients with an MSI-H phenotype had lower AIM levels compared with MSS patients. Moreover, AIM levels were correlated with histological type and MSI status. Logistic regression analysis revealed that decreased AIM levels were independently associated with MSI-H phenotype after adjusting confounding factors. CONCLUSION: Reduced AIM levels are associated with MSI-H subtyping of CRC. Further research on the involvement of AIM in MSI-H CRC is needed.
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spelling pubmed-76540322020-11-10 Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer Huang, Wen-juan Wang, Xin Zhang, Meng-lin Li, Li Wang, Rui-tao BMC Gastroenterol Research Article BACKGROUND: The microsatellite instability (MSI) in colorectal cancer (CRC) has a more favorable clinical outcome and is characterized by highly upregulated expression of various immunological checkpoints than microsatellite stable (MSS) tumors. Apoptosis inhibitor of macrophage (AIM) is a circulating protein and circulates throughout the body to remove cellular debris. The aim of this study was to evaluate the association between MSI status and AIM levels in CRC patients. METHODS: In this study, we evaluated the levels of AIM by Enzyme Linked Immuno-Sorbent Assay (ELISA) in serum of 430 CRC patients. All patients’ clinical and laboratory characteristics at initial diagnosis were collected. The relationship between AIM levels and MSI status was examined. RESULTS: 64 patients (14.9%) were identified as having MSI-H (high-frequency MSI) and 366 casess (85.1%) having MSS. Patients with an MSI-H phenotype had lower AIM levels compared with MSS patients. Moreover, AIM levels were correlated with histological type and MSI status. Logistic regression analysis revealed that decreased AIM levels were independently associated with MSI-H phenotype after adjusting confounding factors. CONCLUSION: Reduced AIM levels are associated with MSI-H subtyping of CRC. Further research on the involvement of AIM in MSI-H CRC is needed. BioMed Central 2020-11-10 /pmc/articles/PMC7654032/ /pubmed/33172404 http://dx.doi.org/10.1186/s12876-020-01520-8 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Huang, Wen-juan
Wang, Xin
Zhang, Meng-lin
Li, Li
Wang, Rui-tao
Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
title Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
title_full Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
title_fullStr Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
title_full_unstemmed Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
title_short Association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
title_sort association between apoptosis inhibitor of macrophage and microsatellite instability status in colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654032/
https://www.ncbi.nlm.nih.gov/pubmed/33172404
http://dx.doi.org/10.1186/s12876-020-01520-8
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