Prognostic and clinicopathological significance of CapG in various cancers: Evidence from a meta-analysis

Pathol Res Pract. 2019 Dec;215(12):152683. doi: 10.1016/j.prp.2019.152683. Epub 2019 Oct 12.

Abstract

Background: The gelsolin-like actin-capping protein (CapG) is an actin-binding protein in the gelsolin superfamily. Increasing evidence indicates that CapG is highly expressed in various types of cancer. However, the role of CapG in malignant tumors is still controversial. Therefore, we conducted a meta-analysis to assess the prognostic value and clinicopathological significance of CapG in malignant tumors.

Method: We searched for eligible studies in the PubMed, Web of Science, Embase, and Cochrane databases. Stata SE12.0 software was used for quantitative meta-analysis. The hazard ratios (HRs) and odds ratios (ORs) with 95% CI were pooled to assess the relationship between CapG expression and overall survival (OS), as well as clinicopathological parameters.

Results: Sixteen studies with a total of 1987 cancer patients were included in this meta-analysis. The results showed that higher CapG expression was statistically correlated with shorter OS (HR 1.70, 95% CI 1.43-1.97, P < 0.001), positive lymph node metastasis (OR 1.91, 95% CI 1.19-3.09, P = 0.008), advanced TNM stage (OR 1.87, 95% CI 1.17-3.00, P = 0.009), advanced T-primary stage (OR 2.54, 95% CI 1.08-6.00, P = 0.033) and male sex (OR 1.77, 95% CI 1.23-2.56, P = 0.002). However, no significant correlation was observed between increased CapG expression and advanced age, larger tumor size, differentiation, or advanced histopathologic grading (P > 0.05).

Conclusions: High CapG expression is associated with a poor prognosis and worse clinicopathological parameters in various cancers. CapG is a potential prognostic biomarker and a possible clinicopathological predictive factor for various cancers.

Keywords: Cancer; CapG; Meta-analysis; Prognosis.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Biomarkers, Tumor / metabolism*
  • Female
  • Humans
  • Lymphatic Metastasis
  • Male
  • Microfilament Proteins / metabolism*
  • Middle Aged
  • Neoplasm Staging
  • Neoplasms / metabolism*
  • Neoplasms / mortality
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Nuclear Proteins / metabolism*
  • Risk Factors
  • Sex Factors
  • Signal Transduction

Substances

  • Biomarkers, Tumor
  • Microfilament Proteins
  • Nuclear Proteins
  • CAPG protein, human