Association between the insulin-like growth factor 1 gene rs2195239 and rs2162679 polymorphisms and cancer risk: a meta-analysis

BMC Med Genet. 2019 Jan 17;20(1):17. doi: 10.1186/s12881-019-0749-3.

Abstract

Background: Many epidemiological studies have suggested that insulin-like growth factor1 (IGF1) gene single-nucleotide polymorphisms (SNPs) may be associated with cancer risk. Among several commonly studied polymorphisms in IGF1 gene, rs2195239 and rs2162679 attracted many attentions. So we perform a meta-analysis to determine potential associations between IGF1 rs2195239 and rs2162679 polymorphisms and cancer risk.

Methods: We retrieved relevant articles from the PubMed, Embase, and Web of Science databases up to April 30, 2018. Ultimately, thirteen studies were included in the present meta-analysis, which involved 12,515 cases and 19,651 controls. The odd ratios (ORs) and their 95% confidence intervals (CIs) were pooled to estimate the strength of the associations.

Results: rs2195239 reduces the overall cancer risk in homozygote model, as well as reducing cancer risk in Asian populations in allele, homozygote, and recessive models. No significant relationship was found between rs2195239 and breast or pancreatic cancer risk. rs2162679 reduces the overall cancer risk in allele, homozygote, dominant, and recessive models, as well as reducing cancer risk in Asian populations in allele, homozygote, and recessive models.

Conclusions: IGF1 rs2195239 and rs2162679 were associated with overall cancer risk based on present studies.

Keywords: Cancer; IGF1; Meta-analysis; Polymorphism; rs2162679; rs2195239.

Publication types

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

MeSH terms

  • Asia
  • Female
  • Gene Frequency
  • Genetic Association Studies / methods*
  • Genetic Predisposition to Disease
  • Humans
  • Insulin-Like Growth Factor I / genetics*
  • Male
  • Neoplasms / genetics*
  • Odds Ratio
  • Polymorphism, Single Nucleotide

Substances

  • IGF1 protein, human
  • Insulin-Like Growth Factor I