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An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma
In this study, we performed bioinformatics and statistical analyses to investigate the prognostic significance of metabolic genes in clear cell renal cell carcinoma (ccRCC) using the transcriptome data of 539 ccRCC and 72 normal renal tissues from TCGA database. We identified 79 upregulated and 45 d...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746370/ https://www.ncbi.nlm.nih.gov/pubmed/33221754 http://dx.doi.org/10.18632/aging.104088 |
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author | Wu, Yue Wei, Xian Feng, Huan Hu, Bintao Liu, Bo Luan, Yang Ruan, Yajun Liu, Xiaming Liu, Zhuo Wang, Shaogang Liu, Jihong Wang, Tao |
author_facet | Wu, Yue Wei, Xian Feng, Huan Hu, Bintao Liu, Bo Luan, Yang Ruan, Yajun Liu, Xiaming Liu, Zhuo Wang, Shaogang Liu, Jihong Wang, Tao |
author_sort | Wu, Yue |
collection | PubMed |
description | In this study, we performed bioinformatics and statistical analyses to investigate the prognostic significance of metabolic genes in clear cell renal cell carcinoma (ccRCC) using the transcriptome data of 539 ccRCC and 72 normal renal tissues from TCGA database. We identified 79 upregulated and 45 downregulated (n=124) metabolic genes in ccRCC tissues. Eleven prognostic metabolic genes (NOS1, ALAD, ALDH3B2, ACADM, ITPKA, IMPDH1, SCD5, FADS2, ACHE, CA4, and HK3) were identified by further analysis. We then constructed an 11-metabolic gene signature-based prognostic risk score model and classified ccRCC patients into high- and low-risk groups. Overall survival (OS) among the high-risk ccRCC patients was significantly shorter than among the low-risk ccRCC patients. Receiver operating characteristic (ROC) curve analysis of the prognostic risk score model showed that the areas under the ROC curve for the 1-, 3-, and 5-year OS were 0.810, 0.738, and 0.771, respectively. Thus, our prognostic model showed favorable predictive power in the TCGA and E-MTAB-1980 ccRCC patient cohorts. We also established a nomogram based on these eleven metabolic genes and validated internally in the TCGA cohort, showing an accurate prediction for prognosis in ccRCC. |
format | Online Article Text |
id | pubmed-7746370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-77463702021-01-04 An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma Wu, Yue Wei, Xian Feng, Huan Hu, Bintao Liu, Bo Luan, Yang Ruan, Yajun Liu, Xiaming Liu, Zhuo Wang, Shaogang Liu, Jihong Wang, Tao Aging (Albany NY) Research Paper In this study, we performed bioinformatics and statistical analyses to investigate the prognostic significance of metabolic genes in clear cell renal cell carcinoma (ccRCC) using the transcriptome data of 539 ccRCC and 72 normal renal tissues from TCGA database. We identified 79 upregulated and 45 downregulated (n=124) metabolic genes in ccRCC tissues. Eleven prognostic metabolic genes (NOS1, ALAD, ALDH3B2, ACADM, ITPKA, IMPDH1, SCD5, FADS2, ACHE, CA4, and HK3) were identified by further analysis. We then constructed an 11-metabolic gene signature-based prognostic risk score model and classified ccRCC patients into high- and low-risk groups. Overall survival (OS) among the high-risk ccRCC patients was significantly shorter than among the low-risk ccRCC patients. Receiver operating characteristic (ROC) curve analysis of the prognostic risk score model showed that the areas under the ROC curve for the 1-, 3-, and 5-year OS were 0.810, 0.738, and 0.771, respectively. Thus, our prognostic model showed favorable predictive power in the TCGA and E-MTAB-1980 ccRCC patient cohorts. We also established a nomogram based on these eleven metabolic genes and validated internally in the TCGA cohort, showing an accurate prediction for prognosis in ccRCC. Impact Journals 2020-11-18 /pmc/articles/PMC7746370/ /pubmed/33221754 http://dx.doi.org/10.18632/aging.104088 Text en Copyright: © 2020 Wu 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 Wu, Yue Wei, Xian Feng, Huan Hu, Bintao Liu, Bo Luan, Yang Ruan, Yajun Liu, Xiaming Liu, Zhuo Wang, Shaogang Liu, Jihong Wang, Tao An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
title | An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
title_full | An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
title_fullStr | An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
title_full_unstemmed | An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
title_short | An eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
title_sort | eleven metabolic gene signature-based prognostic model for clear cell renal cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746370/ https://www.ncbi.nlm.nih.gov/pubmed/33221754 http://dx.doi.org/10.18632/aging.104088 |
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