Clinicopathologic Significance of VHL Gene Alteration in Clear-Cell Renal Cell Carcinoma: An Updated Meta-Analysis and Review

Int J Mol Sci. 2018 Aug 26;19(9):2529. doi: 10.3390/ijms19092529.

Abstract

The von Hippel-Lindau (VHL) gene is inactivated frequently in sporadic clear-cell renal cell carcinomas (ccRCCs) by genetic alteration (mutation, loss of heterozygosity, or promoter hypermethylation). However, the pathological or prognostic significance of VHL gene alteration has not been well defined. We conducted this meta-analysis to evaluate the association between VHL alteration and clinopathologic findings in ccRCCs. We performed a systematic computerized search of online databases, including PubMed, EMBASE, Web of Science, and Google Scholar (up to July 2018). From ten studies, 1,082 patients were included in the pooled analyses of odds ratios (ORs) with 95% confidence intervals (CIs) for pathological features (nuclear grade and disease stage) or hazard ratios (HRs) with 95% CIs for overall survival (OS). VHL alteration was not significantly associated with nuclear grade (OR = 0.79, 95% CI: 0.59⁻1.06, p = 0.12) or disease stage (OR = 1.07, 95% CI: 0.79⁻1.46, p = 0.65). There was also no significant correlation between VHL alteration and OS (HR = 0.75, 95% CI: 0.43⁻1.29, p = 0.30). When we pooled HRs for OS according to the VHL alteration types, the combined HRs were 0.72 (95% CI: 0.47⁻1.11, p = 0.14) for VHL mutations and 1.32 (95% CI: 0.70⁻2.47, p = 0.39) for methylation. In conclusion, this meta-analysis indicates that VHL gene alteration is not significantly associated with the pathological features and survival in patients with ccRCC.

Keywords: meta-analysis; methylation; mutations; renal cell carcinoma; review; von Hippel-Lindau.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Adenocarcinoma, Clear Cell / genetics*
  • Adenocarcinoma, Clear Cell / mortality
  • Adenocarcinoma, Clear Cell / pathology*
  • Carcinoma, Renal Cell / genetics*
  • Carcinoma, Renal Cell / mortality
  • Carcinoma, Renal Cell / pathology*
  • DNA Methylation
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Genetic Variation*
  • Humans
  • Mutation
  • Odds Ratio
  • Prognosis
  • Proportional Hazards Models
  • Publication Bias
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics*

Substances

  • Von Hippel-Lindau Tumor Suppressor Protein