Open Accessp53 p.Pro72Arg (rs1042522) and Mouse Double Minute 2 (MDM2) Single-Nucleotide Polymorphism (SNP) 309 Variants and Their Interaction in Chronic Lymphocytic Leukemia(CLL): A Survey in CLL Patients from Western Iran
Author(s) -
Nasrin Jalilian,
Yosra Maleki,
Ebrahim Shakiba,
Mozaffar Aznab,
Ziba Rahimi,
Mehdi Salimi,
Zohreh Rahimi
Publication year - 2021
Publication title -
international journal of hematology- oncology and stem cell research.
Language(s) - English
Resource type - Journals
eISSN - 2008-3009
pISSN - 2008-2207
DOI - 10.18502/ijhoscr.v15i3.6846
Subject(s) - chronic lymphocytic leukemia , single nucleotide polymorphism , genotype , snp , genotyping , allele , leukemia , mdm2 , allele frequency , genetics , medicine , oncology , gene , immunology , biology , cancer research
Background: Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults. The MDM2 and p53 are interacting proteins that play crucial roles in cell biology. Genetic variations of p53 and MDM2 have been identified in many cancers including CLL; among which are SNP309 in the promoter of MDM2 and SNP codon72 in p53.
Materials and Methods: In this study, we sought to find the impact of two SNPs of p53 and MDM2 in the pathogenesis of CLL. A total of 100 CLL patients and 102 healthy controls were recruited. Genomic DNA was extracted, and genotyping was performed using the PCR-RFLP method. The allele and genotype associations were analyzed using the χ2 test. The gene-gene interaction analysis was studied using GMDR v0.9.
Results: Our study found the absence of a signicant difference between CLL patients and controls related to the allelic frequencies or genotypic distributions for both MDM2 SNP309 and p53 codon72. A significantly higher frequency of p53 C allele was found in patients with disease duration of more than 36 compared to those less than 36 months. However, GMDR analysis suggests genetic interaction between the genes under study.
Conclusion: Our findings indicated each polymorphism of p53 codon72 and MDM2 (SNP309) was not a risk factor for CLL but the p53 C allele could be associated with the disease duration. Besides, the interaction between p53/MDM2 genotypes may confer susceptibility to CLL. Our study could be useful in genetic association studies of CLL and the role of gene-gene interactions in the susceptibility to the disease.