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GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma
GSDM family is a group of critical proteins that mediate pyroptosis and plays an important role in cell death and inflammation. However, their specific function in clear cell renal cell carcinoma (ccRCC, KIRC) have not been clarified comprehensively. In this study, we assessed the roles of the GSDM...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004560/ https://www.ncbi.nlm.nih.gov/pubmed/35321945 http://dx.doi.org/10.18632/aging.203973 |
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author | Yao, Lei Li, Juanni Xu, Zhijie Yan, Yuanliang Hu, Kuan |
author_facet | Yao, Lei Li, Juanni Xu, Zhijie Yan, Yuanliang Hu, Kuan |
author_sort | Yao, Lei |
collection | PubMed |
description | GSDM family is a group of critical proteins that mediate pyroptosis and plays an important role in cell death and inflammation. However, their specific function in clear cell renal cell carcinoma (ccRCC, KIRC) have not been clarified comprehensively. In this study, we assessed the roles of the GSDM family in expression, prognostic value, functional enrichment analysis, genetic alterations, immune infiltration and DNA methylation in ccRCC patients by using different bioinformatics databases. We found that the expression levels of GADMA-E were significantly higher in ccRCC tissues compared with normal tissues, while the expression level of PJVK was decreased. Moreover, survival analysis indicated that upregulation of GSDME was related to poor overall survival (OS) and recurrence-free survival (RFS) of ccRCC patients. The main function of differentially expressed GSDM homologs was related to ion transport. We also found that the expression profiles of the GSDM family were highly correlated with infiltrating immune cells (i.e., CD8+ T cells, CD4+ T cells, B cells, macrophages, neutrophils and dendritic cells), and there were significant differences in the expression of GSDM family in different ccRCC immune subtypes. Furthermore, DNA methylation analysis indicated that the DNA methylation levels of GSDMA/B/D/E were decreased, while the DNA methylation level of PJVK was increased. In conclusion, this study provides integrated information about abnormal GSDM family members as potential biomarkers for the diagnosis and prognosis of ccRCC. Especially, GSDME was a potential clinical target and prognostic biomarkers for patients with ccRCC. |
format | Online Article Text |
id | pubmed-9004560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-90045602022-04-13 GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma Yao, Lei Li, Juanni Xu, Zhijie Yan, Yuanliang Hu, Kuan Aging (Albany NY) Research Paper GSDM family is a group of critical proteins that mediate pyroptosis and plays an important role in cell death and inflammation. However, their specific function in clear cell renal cell carcinoma (ccRCC, KIRC) have not been clarified comprehensively. In this study, we assessed the roles of the GSDM family in expression, prognostic value, functional enrichment analysis, genetic alterations, immune infiltration and DNA methylation in ccRCC patients by using different bioinformatics databases. We found that the expression levels of GADMA-E were significantly higher in ccRCC tissues compared with normal tissues, while the expression level of PJVK was decreased. Moreover, survival analysis indicated that upregulation of GSDME was related to poor overall survival (OS) and recurrence-free survival (RFS) of ccRCC patients. The main function of differentially expressed GSDM homologs was related to ion transport. We also found that the expression profiles of the GSDM family were highly correlated with infiltrating immune cells (i.e., CD8+ T cells, CD4+ T cells, B cells, macrophages, neutrophils and dendritic cells), and there were significant differences in the expression of GSDM family in different ccRCC immune subtypes. Furthermore, DNA methylation analysis indicated that the DNA methylation levels of GSDMA/B/D/E were decreased, while the DNA methylation level of PJVK was increased. In conclusion, this study provides integrated information about abnormal GSDM family members as potential biomarkers for the diagnosis and prognosis of ccRCC. Especially, GSDME was a potential clinical target and prognostic biomarkers for patients with ccRCC. Impact Journals 2022-03-23 /pmc/articles/PMC9004560/ /pubmed/35321945 http://dx.doi.org/10.18632/aging.203973 Text en Copyright: © 2022 Yao et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yao, Lei Li, Juanni Xu, Zhijie Yan, Yuanliang Hu, Kuan GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
title | GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
title_full | GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
title_fullStr | GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
title_full_unstemmed | GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
title_short | GSDMs are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
title_sort | gsdms are potential therapeutic targets and prognostic biomarkers in clear cell renal cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004560/ https://www.ncbi.nlm.nih.gov/pubmed/35321945 http://dx.doi.org/10.18632/aging.203973 |
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