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A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance
Disk-like domain receptor 1 (DDR1) is a crucial regulator of pro-inflammatory mediators and matrix-degrading enzymes. Although mounting evidence supports a vital role for DDR1 in the tumorigenesis of some cancers, no pan-cancer analysis of DDR1 has been reported. Therefore, we aimed to explore the p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082773/ https://www.ncbi.nlm.nih.gov/pubmed/37031216 http://dx.doi.org/10.1038/s41598-023-27975-9 |
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author | Yang, Longfei Zhang, Yuwei Tang, Yifan Wang, Yang Jiang, Peng Liu, Fengping Feng, Ninghan |
author_facet | Yang, Longfei Zhang, Yuwei Tang, Yifan Wang, Yang Jiang, Peng Liu, Fengping Feng, Ninghan |
author_sort | Yang, Longfei |
collection | PubMed |
description | Disk-like domain receptor 1 (DDR1) is a crucial regulator of pro-inflammatory mediators and matrix-degrading enzymes. Although mounting evidence supports a vital role for DDR1 in the tumorigenesis of some cancers, no pan-cancer analysis of DDR1 has been reported. Therefore, we aimed to explore the prognostic value of DDR1 in 33 cancer types and investigate its potential immune function. We used a range of bioinformatics approaches to explore the potential carcinogenic role of DDR1 in multiple cancers. We found that DDR1 was expressed at high levels in most cancers. DDR1 expression was positively or negatively associated with prognosis in different cancers. DDR1 expression was significantly associated with DNA methylation in 8 cancers, while there was a correlation between DDR1 expression and RNA methylation-related genes and mismatch repair gene in most cancers. Furthermore, DDR1 expression was significantly associated with microsatellite instability in 6 cancers and tumor mutation burden in 11 cancers. In addition, DDR1 expression was also significantly correlated with immune cell infiltration, tumor microenvironment, immune-related genes, and drug resistance in various cancers. In conclusion, DDR1 can serve as a potential therapeutic target and prognostic marker for various malignancies due to its vital role in tumorigenesis and tumor immunity. |
format | Online Article Text |
id | pubmed-10082773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100827732023-04-10 A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance Yang, Longfei Zhang, Yuwei Tang, Yifan Wang, Yang Jiang, Peng Liu, Fengping Feng, Ninghan Sci Rep Article Disk-like domain receptor 1 (DDR1) is a crucial regulator of pro-inflammatory mediators and matrix-degrading enzymes. Although mounting evidence supports a vital role for DDR1 in the tumorigenesis of some cancers, no pan-cancer analysis of DDR1 has been reported. Therefore, we aimed to explore the prognostic value of DDR1 in 33 cancer types and investigate its potential immune function. We used a range of bioinformatics approaches to explore the potential carcinogenic role of DDR1 in multiple cancers. We found that DDR1 was expressed at high levels in most cancers. DDR1 expression was positively or negatively associated with prognosis in different cancers. DDR1 expression was significantly associated with DNA methylation in 8 cancers, while there was a correlation between DDR1 expression and RNA methylation-related genes and mismatch repair gene in most cancers. Furthermore, DDR1 expression was significantly associated with microsatellite instability in 6 cancers and tumor mutation burden in 11 cancers. In addition, DDR1 expression was also significantly correlated with immune cell infiltration, tumor microenvironment, immune-related genes, and drug resistance in various cancers. In conclusion, DDR1 can serve as a potential therapeutic target and prognostic marker for various malignancies due to its vital role in tumorigenesis and tumor immunity. Nature Publishing Group UK 2023-04-08 /pmc/articles/PMC10082773/ /pubmed/37031216 http://dx.doi.org/10.1038/s41598-023-27975-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Yang, Longfei Zhang, Yuwei Tang, Yifan Wang, Yang Jiang, Peng Liu, Fengping Feng, Ninghan A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance |
title | A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance |
title_full | A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance |
title_fullStr | A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance |
title_full_unstemmed | A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance |
title_short | A pan-cancer analysis of DDR1 in prognostic signature and tumor immunity, drug resistance |
title_sort | pan-cancer analysis of ddr1 in prognostic signature and tumor immunity, drug resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082773/ https://www.ncbi.nlm.nih.gov/pubmed/37031216 http://dx.doi.org/10.1038/s41598-023-27975-9 |
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