Wu, Chengjiang and Cai, Xiaojie and Yan, Jie and Deng, Anyu and Cao, Yun and Zhu, Xueming (2020) Identification of Novel Glycolysis-Related Gene Signatures Associated With Prognosis of Patients With Clear Cell Renal Cell Carcinoma Based on TCGA. Frontiers in Genetics, 11. ISSN 1664-8021
![[thumbnail of pubmed-zip/versions/2/package-entries/fgene-11-589663-r1/fgene-11-589663.pdf]](http://ebookhub.promo4journal.com/style/images/fileicons/text.png)
pubmed-zip/versions/2/package-entries/fgene-11-589663-r1/fgene-11-589663.pdf - Published Version
Download (3MB)
Abstract
Objective: The purpose of the present study was to detect novel glycolysis-related gene signatures of prognostic values for patients with clear cell renal cell carcinoma (ccRCC).
Methods: Glycolysis-related gene sets were acquired from the Molecular Signatures Database (V7.0). Gene Set Enrichment Analysis (GSEA) software (4.0.3) was applied to analyze glycolysis-related gene sets. The Perl programming language (5.32.0) was used to extract glycolysis-related genes and clinical information of patients with ccRCC. The receiver operating characteristic curve (ROC) and Kaplan–Meier curve were drawn by the R programming language (3.6.3).
Results: The four glycolysis-related genes (B3GAT3, CENPA, AGL, and ALDH3A2) associated with prognosis were identified using Cox proportional regression analysis. A risk score staging system was established to predict the outcomes of patients with ccRCC. The patients with ccRCC were classified into the low-risk group and high-risk group.
Conclusions: We have successfully constructed a risk staging model for ccRCC. The model has a better performance in predicting the prognosis of patients, which may have positive reference value for the treatment and curative effect evaluation of ccRCC.
Item Type: | Article |
---|---|
Subjects: | Bengali Archive > Medical Science |
Depositing User: | Unnamed user with email support@bengaliarchive.com |
Date Deposited: | 30 Jan 2023 10:38 |
Last Modified: | 29 Mar 2025 12:53 |
URI: | http://ebookhub.promo4journal.com/id/eprint/104 |