Vakil Monfared R, Mashayekhi F
Department of Biology, Faculty of Sciences, University of Guilan, Rasht 4193833697, Iran.
Exp Oncol. 2018 Jun;40(2):132-135.
The immune system plays an important role in the breast cancer development. OX40L (also known as TNFSF4), a membrane protein, which is a member of the tumor necrosis factor super family binds to its receptor OX40 and this co-stimulation has a crucial role in T cell proliferation, survival and cytokine release. Previous studies have shown that OX40L is associated with cancer. Due to the importance of the T cells in antitumor activities of OX40L we studied the association of rs3850641 (A→G) polymorphism of OX40L gene with the breast cancer.
The study included 123 women with breast cancer and 126 healthy volunteers with no signs of cancer. Genomic DNA was extracted from blood leucocytes. Genotype and allele frequencies were determined in patients and control cases with the method of polymerase chain reaction-restriction fragment length polymorphism and the statistical analysis was performed by Med Calc.
The prevalence of genotype frequencies of AA/AG/GG were 60.9%, 30.08% and 8.9% in patients with breast cancer cases and 74.6%, 18.25% and 7.14% in healthy volunteers while the A and G allelic frequency was 76.01 and 23.98% in patients and 83.73 and 16.26% in healthy controls, respectively. Statistical analysis has shown significant difference from the comparison of genotype (p = 0.03).
It is concluded that the rs3850641 SNP is significantly associated with the breast cancer susceptibility in Iranian population. However, further studies in larger populations including other genetic and environmental factors are required to achieve conclusion.
免疫系统在乳腺癌发展过程中发挥着重要作用。OX40L(也称为TNFSF4)是一种膜蛋白,属于肿瘤坏死因子超家族成员,它与其受体OX40结合,这种共刺激在T细胞增殖、存活和细胞因子释放中起着关键作用。先前的研究表明OX40L与癌症有关。鉴于T细胞在OX40L抗肿瘤活性中的重要性,我们研究了OX40L基因rs3850641(A→G)多态性与乳腺癌的关联。
该研究纳入了123例乳腺癌女性患者和126名无癌症迹象的健康志愿者。从血液白细胞中提取基因组DNA。采用聚合酶链反应-限制性片段长度多态性方法测定患者和对照病例的基因型和等位基因频率,并通过Med Calc进行统计分析。
乳腺癌患者中AA/AG/GG基因型频率的患病率分别为60.9%、30.08%和8.9%,健康志愿者中分别为74.6%、18.25%和7.14%,而患者中A和G等位基因频率分别为76.01%和23.98%,健康对照中分别为83.73%和16.26%。统计分析表明基因型比较存在显著差异(p = 0.03)。
得出结论,rs3850641单核苷酸多态性与伊朗人群乳腺癌易感性显著相关。然而,需要在包括其他遗传和环境因素的更大人群中进行进一步研究才能得出结论。