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Asian Pac J Cancer Prev ; 23(10): 3577-3585, 2022 Oct 01.
Article in English | MEDLINE | ID: mdl-36308385

ABSTRACT

BACKGROUND: ATM; XRCC6 and LIG4 genes play an important role in repairing the double-strand DNA breaks and maintaining the genome stability. Single nucleotide polymorphisms (SNPs) in these genes could affect these genes expression and function. The aim of this study was to address the effect of SNP of the DNA repairing genes on corresponding  gene expression as well as AML patient's outcome. SUBJECTS AND METHODS: This is cross sectional study included 95 newly diagnosed AML patients. For all subjects included in our study SNPs  and expression of ATM (rs189037G>A), XRCC6 (rs2267437C>G) and LIG4 (rs1805388C>T) genes were evaluated by RFLP and real time PCR. RESULTS: The following SNPs in ATM (AA); XRCC6 (GG); and LIG4 (TT) are associated with down regulation of the corresponding genes (P<0.001). The lower expression of ATM and LIG4 genes are associated with shorter OS and DFS. Cox regression multivariate analysis revealed that lower expression of ATM HR : 2.02 (CI: 1.12-3.64; p=0.020. CONCLUSION: The following SNPs of ATM (AA); XRCC6 (GG); and LIG4 (TT) are associated with down regulation of corresponding genes expression. ATM and XRCC6 lower expression are predictors of OS while ATM is predictor of DFS and could be used for optimizing the AML therapy.


Subject(s)
Leukemia, Myeloid, Acute , Polymorphism, Single Nucleotide , Humans , DNA Ligase ATP/genetics , Cross-Sectional Studies , Leukemia, Myeloid, Acute/genetics , DNA Repair/genetics , Genetic Predisposition to Disease , Genotype
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