Contribution of the GSTM1, GSTP1 and GSTT1 genes polymorphisms from glutationtransferases family to formation of predisposition for cervical cancer in women of Kyrgyz nationality
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Keywords

cervical cancer
GSTM1
GSTP1
GSTT1
Kyrgyz population
intergenic interactions

How to Cite

Isakova , Z., Kipen , V., Юсуфова , М., Aitbaev , K., & Bukuev , N. (2022). Contribution of the GSTM1, GSTP1 and GSTT1 genes polymorphisms from glutationtransferases family to formation of predisposition for cervical cancer in women of Kyrgyz nationality. Voprosy Onkologii, 68(6), 805–813. https://doi.org/10.37469/0507-3758-2022-68-6-805-813

Abstract

  • Assessment of the contribution of polymorphic loci for genes from glutationtransferases family (GSTM1, GSTP1, GSTT1 genes) and their intergenic interactions to the formation of predisposition to cervical cancer (CС) in women of Kyrgyz nationality.
  • Materials and methods. The study included 191 women of the Kyrgyz ethnic group. Among them there were 95 women with the morphologically verified diagnosis of cervical cancer (СC), and 96 women without oncological diseases in their medical history. Genotyping of single-nucleotide polymorphisms (SNPs) was performed using PCR-RFLP for rs1695 GSTP1 Deletion polymorphisms in GSTT1 and GSTM1 genes were determined using allele-specific real-time PCR.
  • Deletion of the GSTM1 gene region was a genetic marker associated with an increased likelihood of developing СС (odds ratio (OR)=2.02, 95% CI 1.28–3.20, p=0.002) among the examined women from Kyrgyzstan. Similar results were obtained for GSTT1 gene ― the deletion of the GSTT1 gene region was also a genetic marker associated with an increased likelihood of developing СС (OR=3.04, 95% CI 2.00–4.64, p<0.0001). Analysis of the polymorphic variant p.Ile105Val (GSTP1 gene) did not reveal statistically significant differences in the frequency of genotypes or alleles distribution between cervical cancer patients and women from the comparison group (p>0.05).
  • The results of the present study confirm the association of combined carrier state of particular variants of GSTM1 and GSTT1 genes and higher likelihood of CC development in Kyrgyz women.
https://doi.org/10.37469/0507-3758-2022-68-6-805-813
##article.numberofdownloads## 192
##article.numberofviews## 94
pdf (Русский)

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