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

被引:12
作者
Wu, Yue [1 ,2 ]
Zhang, Xi [3 ]
Wei, Xian [1 ,2 ]
Feng, Huan [1 ,2 ]
Hu, Bintao [1 ,2 ]
Deng, Zhiyao [1 ,2 ]
Liu, Bo [4 ]
Luan, Yang [1 ,2 ]
Ruan, Yajun [1 ,2 ]
Liu, Xiaming [1 ,2 ]
Liu, Zhuo [1 ,2 ]
Liu, Jihong [1 ,2 ]
Wang, Tao [1 ,2 ]
机构
[1] Huezhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Urol, Wuhan, Peoples R China
[2] Huezhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Inst Urol, Wuhan, Peoples R China
[3] Wuhan Univ, Sch Hlth Sci, Wuhan, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Oncol, Tongji Med Coll, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
clear cell renal cell carcinoma; ubiquitin; prognostic signature; prognosis; bioinformatics; CANCER; PROMOTES; HYPERMETHYLATION; DEGRADATION; CROSSROADS; EXPRESSION; MIGRATION; PROTEINS; LIGASES;
D O I
10.3389/fcell.2021.684643
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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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页数:14
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