Gene network profiling in muscle-invasive bladder cancer: A systematic review and meta-analysis. Review uri icon

Overview

abstract

  • BACKGROUND: Determining meta-analysis of transcriptional profiling of muscle-invasive bladder cancer (MIBC) through Gene Expression Omnibus (GEO) datasets has not been investigated. This study aims to define gene expression profiles in MIBC and to identify potential candidate genes and pathways. OBJECTIVES: To review and evaluate gene expression studies in MIBC through publicly available RNA sequencing (RNA-Seq) and microarray data in order to identify potential prognostic and therapeutic targets for MIBC. METHODS: A systematic literature search of the Ovid MEDLINE, PubMed, and Wiley Cochrane Central Register of Controlled Trials databases was performed using the terms "gene," "gene expression," and "bladder cancer" January 1, 1990 through March 2021 focused on populations with MIBC. RESULTS: In the final analysis, GEO datasets were included. Fixed effect model was employed in the meta-analysis. Gene networking connections and gene-set functional analyses of the identified genes as differentially expressed in MIBC were performed using ImaGEO and GeneMANIA software. A heatmap for the upregulated and downregulated genes was generated along with the correlated pathways. CONCLUSION: A total of 9 genes were reported in this analysis. Six genes were reported as upregulated (ProTα, SPINT1, UBE2E1, RAB25, KPNB1, HDAC1) and 3 genes as downregulated (NUP188, IPO13, NUP124). Genes were found to be involved in "ubiquitin mediated proteolysis," "protein processing in endoplasmic reticulum," "transcriptional misregulation in cancer," and "RNA transport" pathways.

authors

  • Isali, Ilaha
  • McClellan, Phillip
  • Calaway, Adam
  • Prunty, Megan
  • Abbosh, Phillip
  • Mishra, Kirtishri
  • Ponsky, Lee
  • Markt, Sarah
  • Psutka, Sarah P
  • Bukavina, Laura

publication date

  • January 15, 2022

Research

keywords

  • Urinary Bladder Neoplasms

Identity

PubMed Central ID

  • PMC10123538

Scopus Document Identifier

  • 85122943200

Digital Object Identifier (DOI)

  • 10.1016/j.urolonc.2021.11.003

PubMed ID

  • 35039218

Additional Document Info

volume

  • 40

issue

  • 5