Association of Polymorphisms in the Genes of Angiotensinogen and Angiotensin Receptors With Risk for Basal Cell Carcinoma

Anticancer Res. 2019 Oct;39(10):5525-5530. doi: 10.21873/anticanres.13745.

Abstract

Background/aim: Basal cell carcinoma (BCC) has been genetically associated with an increased expression of angiotensin-converting enzyme (ACE), an important factor of the renin-angiotensin system which produces vasoconstrictor angiotensin II. Other factors of this system include angiotensinogen (AGT) and angiotensin receptors AGTR1, AGTR2. We investigated the possible association of BCC with genetic variability in the AGT, AGTR1 and AGTR2 genes.

Materials and methods: DNA samples of 190 Greeks were studied, including 91 patients with BCC and 99 matched healthy controls. Molecular genotyping of patients and controls was performed for the polymorphisms AGT M235T, AGTR1 A1166C and AGTR2 G1675A.

Results: The mutant T allele that increases AGT gene expression was detected in two-fold increased frequency in BCC patients in comparison to healthy controls (p <0.001). On the contrary, no significant difference was observed in AGTR1 and AGTR2 variants between patients and controls.

Conclusion: Increased expression of AGT may be associated with BCC.

Keywords: Angiotensinogen; angiotensin; angiotensin receptors; basal cell carcinoma; cancer risk.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Angiotensinogen / genetics
  • Carcinoma, Basal Cell / genetics*
  • Case-Control Studies
  • Cell Line, Tumor
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic / genetics*
  • Receptor, Angiotensin, Type 1 / genetics
  • Receptor, Angiotensin, Type 2 / genetics
  • Skin Neoplasms / genetics*

Substances

  • AGT protein, human
  • AGTR1 protein, human
  • Receptor, Angiotensin, Type 1
  • Receptor, Angiotensin, Type 2
  • Angiotensinogen