Analysis of the Association between MDM4 rs4245739 Single Nucleotide Polymorphism and Breast Cancer Susceptibility

被引:13
作者
Pedram, Negar [1 ]
Pouladi, Nasser [2 ]
Feizi, Mohammad A. Hosseinpour [3 ]
Montazeri, Vahid [4 ]
Sakhinia, Ebrahim [1 ,5 ]
Estiar, Mehrdad A. [6 ]
机构
[1] Tabriz Univ Med Sci, Sch Med, Div Med Genet, Tabriz, Iran
[2] Azarbaijan Shahid Madani Univ, Fac Sci, Dept Biol, Tabriz, Iran
[3] Univ Tabriz, Fac Nat Sci, Dept Biol, Tabriz, Iran
[4] Nour Nejat Hosp, Dept Thorac Surg, Tabriz, Iran
[5] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[6] Univ Tehran Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
关键词
breast cancer; MDM4; polymorphism; ARMS PCR; TUMOR-FORMATION; P53; DEGRADATION; CONTRIBUTES; PROGRESSION; ONCOGENE; DISEASE; VARIANT; RISK;
D O I
10.7754/Clin.Lab.2016.151128
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: MDM4 is a negative regulator of the p53 tumor suppression pathway. Recent studies have revealed that the rs4245739 A>C polymorphism of MDM4 in the 3'-untranslated region makes it a miR-191 target site which leads to lower MDM4 expression. This study is aimed to detect if rs4245739 single nucleotide polymorphism (SNP) of the MDM4 gene influences the breast cancer development in Iranian-Azeri women. Methods: Blood samples were taken from 260 healthy controls and 220 breast cancer women with ethnicity of Iranian-Azeri. Genotyping was done using Tetra-ARMS PCR. Results: Alleles of MDM4 rs4245739 SNP had no significant different frequency between patients and controls (p > 0.05). Additionally, genotypes of MDM4 rs4245739 SNP did not increase or decrease breast cancer risk in patients when compared to healthy women. Also, there was no significant association between the alleles of MDM4 rs4245739 SNP and clinicopathological factors (p > 0.05). Conclusions: Considering the lack of association between MDM4 rs4245739 polymorphism and breast cancer, rs4245739 polymorphism of this gene seems to have no significant role in the pathophysiology of the disease.
引用
收藏
页码:1303 / 1308
页数:6
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