Prognostic role of microRNA-21 in colorectal cancer: a meta-analysis

PLoS One. 2013 Nov 12;8(11):e80426. doi: 10.1371/journal.pone.0080426. eCollection 2013.

Abstract

Background: To date, many studies have shown that microRNAs (miRNA) exhibit altered expression in various cancers and may play an important role as prognostic biomarker of cancers. The present meta-analysis summarizes the recent advances in the use of microRNA-21 (miR-21) in the assessment of colorectal cancer and analyzes the prognostic role of miR-21 for survival outcome.

Methodology/principal findings: The present meta-analysis was performed by searching PubMed through multiple search strategies. Data were extracted from studies comparing overall survival (OS) in patients with colorectal cancer who showed higher expression of miR-21 than similar patients. Pooled hazard ratios (HRs) of miR-21 for survival and 95% confidence intervals (CI) were calculated. Seven studies with a total of 1174 patients were included this meta-analysis. For overall survival (OS), the pooled hazard ratio (HR) of higher miR-21 expression in colorectal cancer was 1.76 (95% CI: 1.34-2.32, P=0.000). After elimination of heterogeneity, the pooled HR was 2.32 (95% CI: 1.82-2.97, P=0.000), which was found to significantly predict poorer survival. The subgroup analysis suggested that elevated miR-21 level and patients' survival correlated with III/IV stage (HR=5.35, 95% CI: 3.73-7.66).

Conclusions/significance: The present findings suggest that high expression of miR-21 might predict poor prognosis in patients with colorectal cancer.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / mortality*
  • Colorectal Neoplasms / pathology
  • Female
  • Gene Expression
  • Humans
  • Male
  • MicroRNAs / genetics*
  • Neoplasm Staging
  • Prognosis
  • Proportional Hazards Models

Substances

  • Biomarkers, Tumor
  • MIRN21 microRNA, human
  • MicroRNAs

Grants and funding

This work was supported by a grant from the National Natural Science Foundation of China (No. 81001317). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.