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Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study

BACKGROUND: As a transmembrane protein, C-type lectin-like receptor 2 (CLEC-2) is mainly expressed on platelets and released into plasma after platelet activation. Activated platelets participate in the regulation of innate immune cells. Patients with different microsatellite statuses have distinct...

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Autores principales: Zhang, Xin, Yuan, Jia-rui, Wang, Xin, Fu, Shuang, Wang, Rui-tao, Wang, Guang-yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330644/
https://www.ncbi.nlm.nih.gov/pubmed/35902826
http://dx.doi.org/10.1186/s12885-022-09834-4
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author Zhang, Xin
Yuan, Jia-rui
Wang, Xin
Fu, Shuang
Wang, Rui-tao
Wang, Guang-yu
author_facet Zhang, Xin
Yuan, Jia-rui
Wang, Xin
Fu, Shuang
Wang, Rui-tao
Wang, Guang-yu
author_sort Zhang, Xin
collection PubMed
description BACKGROUND: As a transmembrane protein, C-type lectin-like receptor 2 (CLEC-2) is mainly expressed on platelets and released into plasma after platelet activation. Activated platelets participate in the regulation of innate immune cells. Patients with different microsatellite statuses have distinct immune profiles. This study aimed to investigate the association of plasma CLEC-2 levels with microsatellite status among colorectal cancer (CRC) patients. METHODS: A cross-sectional analysis of 430 CRC patients from Harbin Medical University Cancer Hospital was conducted. CLEC-2 levels were measured with fasting venous blood samples drawn from each participant before any treatment. The microsatellite status was evaluated with DNA obtained from fresh frozen tumor tissue samples. The other clinical data were collected and recorded based on the medical system records. RESULTS: CLEC-2 levels were significantly higher among patients with high microsatellite instability phenotype than the stable microsatellite group, adjusting for other confounding variables. CONCLUSIONS: The increased CLEC-2 is associated with the high microsatellite instability subtype of CRC.
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spelling pubmed-93306442022-07-29 Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study Zhang, Xin Yuan, Jia-rui Wang, Xin Fu, Shuang Wang, Rui-tao Wang, Guang-yu BMC Cancer Research BACKGROUND: As a transmembrane protein, C-type lectin-like receptor 2 (CLEC-2) is mainly expressed on platelets and released into plasma after platelet activation. Activated platelets participate in the regulation of innate immune cells. Patients with different microsatellite statuses have distinct immune profiles. This study aimed to investigate the association of plasma CLEC-2 levels with microsatellite status among colorectal cancer (CRC) patients. METHODS: A cross-sectional analysis of 430 CRC patients from Harbin Medical University Cancer Hospital was conducted. CLEC-2 levels were measured with fasting venous blood samples drawn from each participant before any treatment. The microsatellite status was evaluated with DNA obtained from fresh frozen tumor tissue samples. The other clinical data were collected and recorded based on the medical system records. RESULTS: CLEC-2 levels were significantly higher among patients with high microsatellite instability phenotype than the stable microsatellite group, adjusting for other confounding variables. CONCLUSIONS: The increased CLEC-2 is associated with the high microsatellite instability subtype of CRC. BioMed Central 2022-07-28 /pmc/articles/PMC9330644/ /pubmed/35902826 http://dx.doi.org/10.1186/s12885-022-09834-4 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
Zhang, Xin
Yuan, Jia-rui
Wang, Xin
Fu, Shuang
Wang, Rui-tao
Wang, Guang-yu
Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
title Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
title_full Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
title_fullStr Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
title_full_unstemmed Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
title_short Association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
title_sort association between c-type lectin-like receptor 2 and microsatellite instability in colorectal cancer: a cross-sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330644/
https://www.ncbi.nlm.nih.gov/pubmed/35902826
http://dx.doi.org/10.1186/s12885-022-09834-4
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