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Exploring the FGFR3-related oncogenic mechanism in bladder cancer using bioinformatics strategy.


ABSTRACT:

Background

Aberrant activation of fibroblast growth factor receptor 3 (FGFR3) is frequently observed in bladder cancer, but how it involved in carcinogenesis is not well understood. The current study was aimed to investigate the underlying mechanism on the progression of bladder cancer.

Methods

The GSE41035 dataset downloaded from Gene Expression Omnibus was used to identify the differentially expressed genes (DEGs) between bladder cancer cell line RT112 with or without depletion of FGFR3, and gene ontology enrichment analysis was performed. Then, FGFR3-centered protein-protein interaction (PPI) and regulatory networks were constructed. Combined with the data retrieved from GSE31684, prognostic makers for bladder cancer were predicted.

Results

We identified a total of

SUBMITTER: Cao W 

PROVIDER: S-EPMC5359882 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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