AI Article Synopsis

  • The study investigates the connection between single-nucleotide polymorphisms (SNPs) in the angiotensin II receptors and breast cancer among 242 subjects.
  • The results indicate that while SNPs A168G and T1247G showed no significant association with breast cancer, SNP A5235G was linked to an increased risk, with GG genotype appearing protective against the disease.
  • The findings suggest that SNPs A5235G and T1247G could serve as potential genetic markers for breast cancer risk and outcomes, highlighting the complexity of their role in cancer.

Article Abstract

Background: Many types of cancer are associated with polymorphisms of the renin-angiotensin system. Our aim was to assess possible association between single-nucleotide polymorphisms (SNPs) of the angiotensin II receptor types 1 (A168G), and 2 (T1247G and A5235G) with breast cancer.

Patients And Methods: 242 participating subjects were genotyped and allocated to case or control groups.

Results: Genotype distribution (in %) was: for AGTR1 (A168G): AA, AG, GG = 61, 30, 09 for cases, and 69, 25, 06 for controls (p = 0.55); for AGTR2 (T1247G): TT, TG, GG = 84, 12, 04 for cases, and 81, 17, 02 for controls (p = 0.45); for AGTR2 (A5235G): AA, AG, GG = 32, 67, 01 for cases, and 53, 28, 19 for controls (p < 0.0001). Women carrying genotypes AA/AG in the intronic region of angiotensin II type 2 receptor had an 11-fold higher risk of breast cancer than GG carriers.

Conclusions: Many types of cancer have been associated with polymorphisms of the renin-angiotensin system. For SNP A5235G, the GG genotype seems to be protective against breast cancer. The other 2 SNPs showed no association. However, SNPs T1247G and A5235G were associated with at least 1 clinical variable, with G being a predictor of better outcome. The use of SNPs A5235G and T1247G (the latter to a lesser degree) as genetic markers should be considered.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132237PMC
http://dx.doi.org/10.1159/000363429DOI Listing

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