Association of xenobiotic-metabolizing genes polymorphisms with cervical cancer risk in the Tunisian population

Mol Biol Rep. 2023 Feb;50(2):949-959. doi: 10.1007/s11033-022-07945-6. Epub 2022 Nov 14.

Abstract

Background: Host genetic characteristics and environmental factors interactions may play a crucial role in cervical carcinogenesis. We investigated the impact of functional genetic variants of four xenobiotic-metabolizing genes (AhR, CYP1A1, GSTM1, and GSTT1) on cervical cancer development in Tunisian women.

Methods: The AhR gene polymorphism was analyzed using the tetra-primer ARMS-PCR, whereas the CYP1A1 polymorphism genotypes were identified by PCR-RFLP. A multiplex ligation-dependent polymerase chain reaction approach was applied for the analysis of GSTM1 and GSTT1 polymorphisms.

Results: The homozygous A/A genotype of the AhR gene (rs2066853) and the heterozygous T/C genotype of the CYP1A1 SNP (CYP1A1-MspI) appeared to be associated with an increased risk of cervical tumorigenesis (ORa = 2.81; ORa = 5.52, respectively). Furthermore, a significantly increased risk of cervical cancer was associated with the GSTT1 null genotype (ORa = 2.65). However, the null GSTM1 genotype showed any significant association with the risk of cervical cancer compared to the wild genotype (ORa = 1.18; p = 0.784). Considering the combined effect, we noted a significantly higher association with cancer risk for individuals with at least two high-risk genotypes of CYP1A1/GSTT1 (ORa = 4.2), individuals with at least two high-risk genotypes of CYP1A1/GSTT1/AhR (ORa = 11.3) and individuals with at least two high-risk genotypes of CYP1A1/GSTM1/GSTT1/AhR exploitation low-risk genotype as a reference.

Conclusion: This study indicated that the single-gene contribution and the combined effect of xenobiotic-metabolizing gene polymorphisms (AhR, CYP1A1-MspI, GSTM1, and GSTT1) may have a considerable association with increased cervical cancer risk.

Keywords: AhR; And GSTT1; CYP1A1; Cervical cancer; GSTM1; Xenobiotic-metabolizing genes.

MeSH terms

  • Case-Control Studies
  • Cytochrome P-450 CYP1A1* / genetics
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Glutathione Transferase / genetics
  • Humans
  • Polymorphism, Genetic
  • Risk Factors
  • Uterine Cervical Neoplasms* / genetics
  • Xenobiotics

Substances

  • Cytochrome P-450 CYP1A1
  • Xenobiotics
  • Glutathione Transferase