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Polymorphisms of P53 Promoter and Susceptibility to Uterine Leiomyoma Publisher Pubmed



Ziaei E1, 2 ; Chaleshtori MH2 ; Ziaei A3 ; Dehkordi GB2 ; Pooryamofrad A1 ; Kashani S1 ; Batenipoor M1 ; Miraj S4
Authors
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Authors Affiliations
  1. 1. Stud. Research Committee, Shahrekord University of Medical Sciences, Shahrekord, Iran
  2. 2. Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran
  3. 3. Medical Stud. Research Center, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Obstetrics and Gynecology Department, Shahrekord University of Medical Sciences, P.O. Box: 88155, Shahrkord, 137, Iran

Source: Clinical and Experimental Obstetrics and Gynecology Published:2016


Abstract

Background: Uterine leiomyomas could be considered as benign tumor of human uterus smooth muscle with unknown etiology and pathophysiology. Furthermore, they are the most common indication of hysterectomy. The tumor suppressor gene p53 has been involved in various malignancies. Mutation in its promoter site may play a role in tumorigenesis of many malignancies including leiomyoma. Materials and Methods: For study of polymorphisms and allele frequency, 234 female patients with pathologically diagnosed uterine leiomyoma and 100 healthy blood donors as control group were assessed. DNAs were extracted from peripheral blood cells, amplified using polymerase chain reaction and restriction fragment length polymorphism (RFLP) technique was utilized for their analysis. Result: Proportions of A homozygote/heterozygote/G homozygote for SNP -250 A/G in leiomyoma group were 97.8%, 1.7%, and 0.4%, and in control group 97%, 3%, and 0%, respectively. In case of-216 T/C polymorphism, proportions of T homozygote/heterozygote/C homozygote in leiomyoma were 98%, 1.7%, and 0%, and in control samples 98%, 2%, and 0%, respectively. Genotype frequency of A homozygote/heterozygote/G homozygote for SNP-103 A/G was 97.9%, 1.7%, and 0.4% in leiomyoma group, and 98%, 2%, and 0% in control group, respectively. Proportions of A homozygote/heterozygote/G homozygote for SNP-33 A/G in leiomyoma group were 97.8%, 2.2%, and 0%, and 97%, 3%, and 0% in case samples, respectively. Discussion: Based on the present results in an Iranian female population, surprisingly there was no significant differences between leiomyoma cases and control samples regarding allele frequencies of p53 promoter polymorphism. Therefore, The p53 promoter polymorphism is not associated with the susceptibility of uterine leiomyomas in Iranian women.