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Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma
Objective: To explore fatty acid metabolism-related genes and signature, which could predict survival outcomes of clear cell renal carcinoma (ccRCC) patients. Materials and Methods: Transcriptional and survival data of fatty acid genes in ccRCC patients were retrieved from UCSC Xena and Geo DataSets...
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/PMC9831735/ https://www.ncbi.nlm.nih.gov/pubmed/36516496 http://dx.doi.org/10.18632/aging.204433 |
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author | Wang, Rongjiang Shen, Junwen Chen, Yu Gao, Jianguo Yao, Jianxiang |
author_facet | Wang, Rongjiang Shen, Junwen Chen, Yu Gao, Jianguo Yao, Jianxiang |
author_sort | Wang, Rongjiang |
collection | PubMed |
description | Objective: To explore fatty acid metabolism-related genes and signature, which could predict survival outcomes of clear cell renal carcinoma (ccRCC) patients. Materials and Methods: Transcriptional and survival data of fatty acid genes in ccRCC patients were retrieved from UCSC Xena and Geo DataSets. We first performed Lasso Cox regression analysis to identify survival-related genes. These genes were then used to construct metabolic-related gene signature and risk score. Enrichment analysis and immune component and chemotherapy response prediction were also performed. Results: In total, five survival-related genes were identified: AGR2, HAO2, IGF2BP1, MCCD1 and OLFM4 (p < 0.05). A series of survival value analyses revealed survival-related signature and risk score, including KM analysis (training set: p < 0.001; test set: p = 0.008). Four clinical indexes (T stage, N stage, M stage, and pathology) were positively correlated with risk score. Time-dependent ROC analysis yielded AUC value of 0.813. Immune landscape analysis revealed that risk score was strongly correlated with TAM score and cytotoxic score. Patients with high risk score and TAM score or cytotoxic score had the shortest survival time. Finally, inhibition of fatty acid metabolism in human ccRCC cell line produced corresponding changes in five genes, consistent with our preliminary results. Conclusion: We identified five survival-related genes (AGR2, HAO2, IGF2BP1, MCCD1 and OLFM4) in ccRCC patients. Our results also indicated that survival-related signature based on these genes is a potential robust prognostic biomarker for ccRCC in patients. |
format | Online Article Text |
id | pubmed-9831735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-98317352023-01-11 Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma Wang, Rongjiang Shen, Junwen Chen, Yu Gao, Jianguo Yao, Jianxiang Aging (Albany NY) Research Paper Objective: To explore fatty acid metabolism-related genes and signature, which could predict survival outcomes of clear cell renal carcinoma (ccRCC) patients. Materials and Methods: Transcriptional and survival data of fatty acid genes in ccRCC patients were retrieved from UCSC Xena and Geo DataSets. We first performed Lasso Cox regression analysis to identify survival-related genes. These genes were then used to construct metabolic-related gene signature and risk score. Enrichment analysis and immune component and chemotherapy response prediction were also performed. Results: In total, five survival-related genes were identified: AGR2, HAO2, IGF2BP1, MCCD1 and OLFM4 (p < 0.05). A series of survival value analyses revealed survival-related signature and risk score, including KM analysis (training set: p < 0.001; test set: p = 0.008). Four clinical indexes (T stage, N stage, M stage, and pathology) were positively correlated with risk score. Time-dependent ROC analysis yielded AUC value of 0.813. Immune landscape analysis revealed that risk score was strongly correlated with TAM score and cytotoxic score. Patients with high risk score and TAM score or cytotoxic score had the shortest survival time. Finally, inhibition of fatty acid metabolism in human ccRCC cell line produced corresponding changes in five genes, consistent with our preliminary results. Conclusion: We identified five survival-related genes (AGR2, HAO2, IGF2BP1, MCCD1 and OLFM4) in ccRCC patients. Our results also indicated that survival-related signature based on these genes is a potential robust prognostic biomarker for ccRCC in patients. Impact Journals 2022-12-12 /pmc/articles/PMC9831735/ /pubmed/36516496 http://dx.doi.org/10.18632/aging.204433 Text en Copyright: © 2022 Wang 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 Wang, Rongjiang Shen, Junwen Chen, Yu Gao, Jianguo Yao, Jianxiang Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
title | Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
title_full | Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
title_fullStr | Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
title_full_unstemmed | Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
title_short | Fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
title_sort | fatty acid metabolism-related signature predicts survival in patients with clear cell renal carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831735/ https://www.ncbi.nlm.nih.gov/pubmed/36516496 http://dx.doi.org/10.18632/aging.204433 |
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