The relationship between VDR polymorphisms and keratinocyte carcinomas: a systematic review and meta-analysis

Future Oncol. 2022 Jul;18(23):2613-2626. doi: 10.2217/fon-2021-1632. Epub 2022 Jul 5.

Abstract

Aim: To perform a meta-analysis to assess the association between common VDR polymorphisms (Fok1, Taq1, Apa1, Bsm1) and keratinocyte carcinomas (KCs) susceptibility. Methods & materials: databases were searched up to November 2021. Odds ratios (ORs) with 95% CIs were evaluated in the association. Results: This meta-analysis included seven articles. KC (and its subtypes) risks are found to be associated with Fok1 (BCC: ff vs FF+Ff: OR = 2.13, 95% CI = 1.14-3.97; SCC: ff vs FF+Ff: OR = 1.54, 95% CI = 1.09-2.18) and Taq1 (BCC: Tt vs TT: OR = 1.99, 95% CI = 1.35-2.93; tt vs TT: OR = 2.09, 95% CI = 1.27-3.43; Tt +tt vs TT: OR = 2.02, 95% CI = 1.41-2.90) polymorphisms. Conclusion: This study suggests that the Fok1 f allele and the Taq1 t allele are associated with increased susceptibility to KC and its subtypes.

Keywords: VDR; basal cell carcinoma; keratinocyte carcinoma; meta-analysis; polymorphism; squamous cell carcinoma.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Alleles
  • Carcinoma*
  • Genetic Predisposition to Disease
  • Humans
  • Keratinocytes
  • Polymorphism, Genetic
  • Receptors, Calcitriol* / genetics

Substances

  • Receptors, Calcitriol
  • VDR protein, human