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Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma

Clear cell renal cell carcinoma (ccRCC) is a common tumor type in genitourinary system and has a poor prognosis. Ubiquitin dependent modification systems have been reported in a variety of malignancies and have influenced tumor genesis and progression. However, the molecular characteristics and prog...

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Autores principales: Wu, Yue, Zhang, Xi, Wei, Xian, Feng, Huan, Hu, Bintao, Deng, Zhiyao, Liu, Bo, Luan, Yang, Ruan, Yajun, Liu, Xiaming, Liu, Zhuo, Liu, Jihong, Wang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258262/
https://www.ncbi.nlm.nih.gov/pubmed/34239875
http://dx.doi.org/10.3389/fcell.2021.684643
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author Wu, Yue
Zhang, Xi
Wei, Xian
Feng, Huan
Hu, Bintao
Deng, Zhiyao
Liu, Bo
Luan, Yang
Ruan, Yajun
Liu, Xiaming
Liu, Zhuo
Liu, Jihong
Wang, Tao
author_facet Wu, Yue
Zhang, Xi
Wei, Xian
Feng, Huan
Hu, Bintao
Deng, Zhiyao
Liu, Bo
Luan, Yang
Ruan, Yajun
Liu, Xiaming
Liu, Zhuo
Liu, Jihong
Wang, Tao
author_sort Wu, Yue
collection PubMed
description Clear cell renal cell carcinoma (ccRCC) is a common tumor type in genitourinary system and has a poor prognosis. Ubiquitin dependent modification systems have been reported in a variety of malignancies and have influenced tumor genesis and progression. However, the molecular characteristics and prognostic value of ubiquitin in ccRCC have not been systematically reported. In our study, 204 differentially expressed ubiquitin related genes (URGs) were identified from The Cancer Genome Atlas (TCGA) cohort, including 141 up-regulated and 63 down-regulated URGs. A total of seven prognostic related URGs (CDCA3, CHFR, CORO6, RNF175, TRIM72, VAV3, and WDR72) were identified by Cox regression analysis of differential URGs and used to construct a prognostic signature. Kaplan-Meier analysis confirmed that high-risk patients had a worse prognosis (P = 1.11e-16), and the predicted area under the receiver operating characteristic (ROC) curves were 0.735 at 1 year, 0.702 at 3 years, and 0.744 at 5 years, showing good prediction accuracy. Stratified analysis showed that the URGs-based prognostic signature could be used to evaluate tumor progression in ccRCC. Further analysis confirmed that the signature is an independent prognostic factor related to the prognosis of ccRCC patients, which may help to reveal the molecular mechanism of ccRCC and provide potential diagnostic and prognostic markers for ccRCC.
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spelling pubmed-82582622021-07-07 Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma Wu, Yue Zhang, Xi Wei, Xian Feng, Huan Hu, Bintao Deng, Zhiyao Liu, Bo Luan, Yang Ruan, Yajun Liu, Xiaming Liu, Zhuo Liu, Jihong Wang, Tao Front Cell Dev Biol Cell and Developmental Biology Clear cell renal cell carcinoma (ccRCC) is a common tumor type in genitourinary system and has a poor prognosis. Ubiquitin dependent modification systems have been reported in a variety of malignancies and have influenced tumor genesis and progression. However, the molecular characteristics and prognostic value of ubiquitin in ccRCC have not been systematically reported. In our study, 204 differentially expressed ubiquitin related genes (URGs) were identified from The Cancer Genome Atlas (TCGA) cohort, including 141 up-regulated and 63 down-regulated URGs. A total of seven prognostic related URGs (CDCA3, CHFR, CORO6, RNF175, TRIM72, VAV3, and WDR72) were identified by Cox regression analysis of differential URGs and used to construct a prognostic signature. Kaplan-Meier analysis confirmed that high-risk patients had a worse prognosis (P = 1.11e-16), and the predicted area under the receiver operating characteristic (ROC) curves were 0.735 at 1 year, 0.702 at 3 years, and 0.744 at 5 years, showing good prediction accuracy. Stratified analysis showed that the URGs-based prognostic signature could be used to evaluate tumor progression in ccRCC. Further analysis confirmed that the signature is an independent prognostic factor related to the prognosis of ccRCC patients, which may help to reveal the molecular mechanism of ccRCC and provide potential diagnostic and prognostic markers for ccRCC. Frontiers Media S.A. 2021-06-22 /pmc/articles/PMC8258262/ /pubmed/34239875 http://dx.doi.org/10.3389/fcell.2021.684643 Text en Copyright © 2021 Wu, Zhang, Wei, Feng, Hu, Deng, Liu, Luan, Ruan, Liu, Liu, Liu and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Wu, Yue
Zhang, Xi
Wei, Xian
Feng, Huan
Hu, Bintao
Deng, Zhiyao
Liu, Bo
Luan, Yang
Ruan, Yajun
Liu, Xiaming
Liu, Zhuo
Liu, Jihong
Wang, Tao
Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma
title Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma
title_full Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma
title_fullStr Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma
title_full_unstemmed Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma
title_short Development of an Individualized Ubiquitin Prognostic Signature for Clear Cell Renal Cell Carcinoma
title_sort development of an individualized ubiquitin prognostic signature for clear cell renal cell carcinoma
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258262/
https://www.ncbi.nlm.nih.gov/pubmed/34239875
http://dx.doi.org/10.3389/fcell.2021.684643
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