Predictive role of the overexpression for CXCR4, C-Met, and VEGF-C among breast cancer patients: A meta-analysis

Breast. 2016 Aug:28:45-53. doi: 10.1016/j.breast.2016.04.016. Epub 2016 May 20.

Abstract

Background: The overexpression of CXCR4, C-Met and VEGF-C present widely in breast tumors, they may be markers of resistance to treatment. However, the studies are still controversial. Thus, this meta-analysis aims to research the relationship between the overexpression of CXCR4, C-Met, VEGF-C and clinical prognosis among breast cancer patients.

Methods: PubMed and EMBASE databases were searched for eligible literature. The outcomes of interest were progression-free survival (PFS), relapse-free survival (RFS) and overall survival (OS). All tests of statistical significance were two sided.

Results: A total of 7830 patients from 28 eligible studies were assessed. The overexpression of the CXCR4 and C-Met both implied significantly worse PFS compared with normal expression [HR = 2.56, 95% CI = 1.34-4.91, P = 0.005; and HR = 1.63 95% CI = 1.20-2.22, P = 0.002]. Meanwhile, if patients had high expression of CXCR4, they would have worse OS [HR = 2.56 95% CI = 1.52-4.31, P = 0.000]. However, the overexpression of C-Met did not relate to OS for breast cancer patients [HR = 1.16, 95% CI = 0.69-1.95, P = 0.570]. Meanwhile, no statistically significant different was observed with respect to PFS and OS between VEGF-C overexpression and normal expression [HR = 0.99, 95% CI = 0.64-1.52, P = 0.968; and HR = 0.76, 95% CI = 0.43-1.33, P = 0.333].

Conclusions: Our meta-analysis showed that CXCR4 and C-Met were efficient prognostic factors for breast cancer. Nevertheless, highly expressing VEGF-C was not related to progression-free survival and overall survival. Due to the small samples and insufficient date, further studies should be conducted to clarify the association between the overexpression of CXCR4 or C-Met or VEGF-C and the prognosis about breast cancer patients.

Keywords: Breast cancer; C-Met; CXCR4; Overexpression; VEGF-C.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Breast Neoplasms / genetics*
  • Disease-Free Survival
  • Female
  • Humans
  • Predictive Value of Tests
  • Proto-Oncogene Proteins c-met / genetics*
  • Receptors, CXCR4 / genetics*
  • Survival Rate
  • Vascular Endothelial Growth Factor C / genetics*

Substances

  • CXCR4 protein, human
  • Receptors, CXCR4
  • Vascular Endothelial Growth Factor C
  • Proto-Oncogene Proteins c-met