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A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect
BACKGROUND: Collagen VI family (COL6A) is a major member of extracellular matrix protein. There is accumulating evidence that COL6A is involved in tumorigenesis and tumor progression. In this study, we performed a systematic analysis of COL6A in pan-cancer based on their molecular features and clini...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513866/ https://www.ncbi.nlm.nih.gov/pubmed/36167487 http://dx.doi.org/10.1186/s12859-022-04951-0 |
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author | Li, Xiang Li, Zeng Gu, Shanzhi Zhao, Xinhan |
author_facet | Li, Xiang Li, Zeng Gu, Shanzhi Zhao, Xinhan |
author_sort | Li, Xiang |
collection | PubMed |
description | BACKGROUND: Collagen VI family (COL6A) is a major member of extracellular matrix protein. There is accumulating evidence that COL6A is involved in tumorigenesis and tumor progression. In this study, we performed a systematic analysis of COL6A in pan-cancer based on their molecular features and clinical significance. METHODS: Based on updated public databases, we integrated several bioinformatics analysis methods to investigate the expression levels of COL6A as well as the relationship between their expression and patient survival, immune subtypes, tumor microenvironment, stemness scores, drug sensitivity, and DNA methylation. RESULTS: The expression levels of COL6A members varied in different cancers, suggesting their expression was cancer-dependent. Among COL6A members, COL6A1/2/3 were predicted poor prognosis in specific cancers. Furthermore, COL6A1/2/3 expression levels revealed a clear correlation with immune subtypes, and COL6A1/2/3 were associated with tumor purity, that is, gene expression levels were generally higher in tumors with higher stromal scores and immune scores. COL6A1/2/3 had a significantly negative correlation with RNA stemness scores, and meanwhile they were also related to DNA stemness scores in different degrees. In addition, the expression of COL6A1/2/3 was significantly related to drug sensitivity of cancer cells. Finally, our study revealed that COL6A1/2/3 expression was mainly negatively correlated with gene methylation, and the methylation levels showed remarkable differences in various cancers. CONCLUSIONS: These findings highlight both the similarities and differences in the molecular characteristics of COL6A members in pan-cancer, and provide comprehensive insights for further investigation into the mechanism of COL6A. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04951-0. |
format | Online Article Text |
id | pubmed-9513866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95138662022-09-28 A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect Li, Xiang Li, Zeng Gu, Shanzhi Zhao, Xinhan BMC Bioinformatics Research BACKGROUND: Collagen VI family (COL6A) is a major member of extracellular matrix protein. There is accumulating evidence that COL6A is involved in tumorigenesis and tumor progression. In this study, we performed a systematic analysis of COL6A in pan-cancer based on their molecular features and clinical significance. METHODS: Based on updated public databases, we integrated several bioinformatics analysis methods to investigate the expression levels of COL6A as well as the relationship between their expression and patient survival, immune subtypes, tumor microenvironment, stemness scores, drug sensitivity, and DNA methylation. RESULTS: The expression levels of COL6A members varied in different cancers, suggesting their expression was cancer-dependent. Among COL6A members, COL6A1/2/3 were predicted poor prognosis in specific cancers. Furthermore, COL6A1/2/3 expression levels revealed a clear correlation with immune subtypes, and COL6A1/2/3 were associated with tumor purity, that is, gene expression levels were generally higher in tumors with higher stromal scores and immune scores. COL6A1/2/3 had a significantly negative correlation with RNA stemness scores, and meanwhile they were also related to DNA stemness scores in different degrees. In addition, the expression of COL6A1/2/3 was significantly related to drug sensitivity of cancer cells. Finally, our study revealed that COL6A1/2/3 expression was mainly negatively correlated with gene methylation, and the methylation levels showed remarkable differences in various cancers. CONCLUSIONS: These findings highlight both the similarities and differences in the molecular characteristics of COL6A members in pan-cancer, and provide comprehensive insights for further investigation into the mechanism of COL6A. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04951-0. BioMed Central 2022-09-27 /pmc/articles/PMC9513866/ /pubmed/36167487 http://dx.doi.org/10.1186/s12859-022-04951-0 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 Li, Xiang Li, Zeng Gu, Shanzhi Zhao, Xinhan A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect |
title | A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect |
title_full | A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect |
title_fullStr | A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect |
title_full_unstemmed | A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect |
title_short | A pan-cancer analysis of collagen VI family on prognosis, tumor microenvironment, and its potential therapeutic effect |
title_sort | pan-cancer analysis of collagen vi family on prognosis, tumor microenvironment, and its potential therapeutic effect |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513866/ https://www.ncbi.nlm.nih.gov/pubmed/36167487 http://dx.doi.org/10.1186/s12859-022-04951-0 |
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