miRNA-767 and its binding site polymorphism in the mTOR gene act as potential biomarkers for female reproductive cancers

Future Oncol. 2023 Sep;19(28):1929-1943. doi: 10.2217/fon-2022-1055. Epub 2023 Oct 2.

Abstract

Aims: The present study aimed to understand the relationship between the mTOR gene SNP (rs2536) and reproductive cancer risk. The expression level of miRNA-767 was also assessed. Methods: 700 tumor samples (300 breast, 200 ovarian and 200 cervical cancers), along with adjacent uninvolved control tissue, were used. rs2536 was screened using Tetra-ARMS PCR and expression level of miRNA-767 was assessed using quantitative PCR. Results: The frequency of the homozygous mutant genotype of rs2536 was observed significantly higher in breast (p < 0.04), ovarian (p < 0.005) and cervical (p < 0.003) cancers. Significant downregulation of miRNA-767 was observed in tumors compared with controls. Conclusion: The present study demonstrates that increased mutant frequency of rs2536 and deregulation of miRNA-767 are associated with increased reproductive cancer risk.

Keywords: SNP; breast cancer; cervical cancer; mTOR; ovarian cancer; reproductive cancers; rs2536.

MeSH terms

  • Binding Sites
  • Biomarkers
  • Biomarkers, Tumor / genetics
  • Breast Neoplasms*
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Polymorphism, Single Nucleotide
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Uterine Cervical Neoplasms* / diagnosis
  • Uterine Cervical Neoplasms* / genetics

Substances

  • Biomarkers
  • Biomarkers, Tumor
  • MicroRNAs
  • MIRN-767 microRNA, human
  • TOR Serine-Threonine Kinases
  • MTOR protein, human