Bioinformatic identification of prognostic signature defined by copy number alteration and expression of CCNE1 in non-muscle invasive bladder cancer.
- Author:
Bic Na SONG
1
;
Seon Kyu KIM
;
In Sun CHU
Author Information
- Publication Type:Original Article
- MeSH: Biodiversity; Cohort Studies; Computational Biology*; Disease Progression; Gene Expression; Gene Regulatory Networks; Genome; Humans; Multivariate Analysis; Population Characteristics; Risk Factors; Transcriptome; Urinary Bladder Neoplasms*; Urinary Bladder*
- From:Experimental & Molecular Medicine 2017;49(1):e282-
- CountryRepublic of Korea
- Language:English
- Abstract: Non-muscle invasive bladder cancer (NMIBC) patients frequently fail to respond to treatment and experience disease progression because of their clinical and biological diversity. In this study, we identify a prognostic molecular signature for predicting the heterogeneity of NMIBC by using an integrative analysis of copy number and gene expression data. We analyzed the copy number and gene expression profiles of 404 patients with bladder cancer obtained from The Cancer Genome Atlas (TCGA) consortium. Of the 14 molecules with significant copy number alterations that were previously reported, 13 were significantly correlated with copy number and expression changes. Prognostic gene sets based on the 13 genes were developed, and their prognostic values were verified in three independent patient cohorts (n=501). Among them, a signature of CCNE1 and its coexpressed genes was significantly associated with disease progression and validated in the independent cohorts. The CCNE1 signature was an independent risk factor based on the result of a multivariate analysis (hazard ratio=6.849, 95% confidence interval=1.613–29.092, P=0.009). Finally, gene network and upstream regulator analyses revealed that NMIBC progression is potentially mediated by CCND1-CCNE1-SP1 pathways. The prognostic molecular signature defined by copy number and expression changes of CCNE1 suggests a novel diagnostic tool for predicting the likelihood of NMIBC progression.
