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COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer

Breast cancer is the malignant tumor with the highest incidence rate at present, and its incidence rate ranks first in the female population. COL11A1 is an important component of collagen XI and is considered to play an important role in a variety of connective tissue diseases. Recent studies have s...

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Autores principales: Luo, Qi, Li, Jinsui, Su, Xiaohan, Tan, Qiao, Zhou, Fangfang, Xie, Shaoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500398/
https://www.ncbi.nlm.nih.gov/pubmed/36160004
http://dx.doi.org/10.3389/fgene.2022.935860
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author Luo, Qi
Li, Jinsui
Su, Xiaohan
Tan, Qiao
Zhou, Fangfang
Xie, Shaoli
author_facet Luo, Qi
Li, Jinsui
Su, Xiaohan
Tan, Qiao
Zhou, Fangfang
Xie, Shaoli
author_sort Luo, Qi
collection PubMed
description Breast cancer is the malignant tumor with the highest incidence rate at present, and its incidence rate ranks first in the female population. COL11A1 is an important component of collagen XI and is considered to play an important role in a variety of connective tissue diseases. Recent studies have shown that COL11A1 is associated with the occurrence and development of many kinds of malignant tumors. However, its prognostic value in breast cancer and its correlation with immune cell infiltration in tumor tissue are not clear. In this paper, we reveal the prognostic value of COL11A1 in breast cancer and its tumor immune-related function through in-depth bioinformatics analysis. The expression of COL11A1 is abnormally upregulated in breast cancer and is significantly related to the poor prognosis of breast cancer. In the analysis of the clinical characteristics of the patients, we found that the expression level of COLL11A1 was closely related to lymph node metastasis, PAM50 (Prediction Analysis of Microarray 50) expression, clinical stage and so on. Gene Ontology (GO) and Kyoto Encyclopedia of Gene and Genome (KEGG) all suggest that COL11A1 is related to tumor immunity. Further study found that the COL11A1 expression was significantly correlated with the degree of immune infiltration and the expression of a variety of immune cell markers in tumor tissue. More importantly, COL11A1 can affect the prognosis of breast cancer patients by participating in the regulation of tumor immune infiltration. Therefore, we believe that COL11A1 is a very potential target for diagnosis and treatment of breast cancer.
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spelling pubmed-95003982022-09-24 COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer Luo, Qi Li, Jinsui Su, Xiaohan Tan, Qiao Zhou, Fangfang Xie, Shaoli Front Genet Genetics Breast cancer is the malignant tumor with the highest incidence rate at present, and its incidence rate ranks first in the female population. COL11A1 is an important component of collagen XI and is considered to play an important role in a variety of connective tissue diseases. Recent studies have shown that COL11A1 is associated with the occurrence and development of many kinds of malignant tumors. However, its prognostic value in breast cancer and its correlation with immune cell infiltration in tumor tissue are not clear. In this paper, we reveal the prognostic value of COL11A1 in breast cancer and its tumor immune-related function through in-depth bioinformatics analysis. The expression of COL11A1 is abnormally upregulated in breast cancer and is significantly related to the poor prognosis of breast cancer. In the analysis of the clinical characteristics of the patients, we found that the expression level of COLL11A1 was closely related to lymph node metastasis, PAM50 (Prediction Analysis of Microarray 50) expression, clinical stage and so on. Gene Ontology (GO) and Kyoto Encyclopedia of Gene and Genome (KEGG) all suggest that COL11A1 is related to tumor immunity. Further study found that the COL11A1 expression was significantly correlated with the degree of immune infiltration and the expression of a variety of immune cell markers in tumor tissue. More importantly, COL11A1 can affect the prognosis of breast cancer patients by participating in the regulation of tumor immune infiltration. Therefore, we believe that COL11A1 is a very potential target for diagnosis and treatment of breast cancer. Frontiers Media S.A. 2022-09-09 /pmc/articles/PMC9500398/ /pubmed/36160004 http://dx.doi.org/10.3389/fgene.2022.935860 Text en Copyright © 2022 Luo, Li, Su, Tan, Zhou and Xie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Luo, Qi
Li, Jinsui
Su, Xiaohan
Tan, Qiao
Zhou, Fangfang
Xie, Shaoli
COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
title COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
title_full COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
title_fullStr COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
title_full_unstemmed COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
title_short COL11A1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
title_sort col11a1 serves as a biomarker for poor prognosis and correlates with immune infiltration in breast cancer
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500398/
https://www.ncbi.nlm.nih.gov/pubmed/36160004
http://dx.doi.org/10.3389/fgene.2022.935860
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