Khadidja Sedrati, Ouarda Semmame, H. Ziada, Ibtissem Boudokhane, N. Abadi
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引用次数: 0
摘要
TP53是一种肿瘤抑制基因,参与多种癌症的发展。据报道,该基因密码子72的单核苷酸多态性导致脯氨酸被精氨酸取代,可能增加致癌风险。本研究的目的是评估Arg72Pro多态性的频率,并寻找这种多态性与癌症发生之间的可能关联。我们的研究涉及从康斯坦丁大学生物学和分子遗传学实验室的DNA库中收集的82个DNA样本,并将2个人群分为两组:41个对照组和41个患有乳腺癌、宫颈癌和肺癌三种癌症之一的患者。采用PCR / RFLP检测该多态性。我们的研究结果显示,两组患者与对照组的杂合子CG基因型有显著差异(OR = 0.13, P = 0.001),可以得出CG基因型是癌症发生的危险因素的结论。然而,本研究显示,与对照组相比,患者的Pro等位基因和Arg等位基因没有差异(OR = 0.95, P = 0.87),这可以排除Arg72Pro多态性与癌症发病之间可能存在的关联。
Impact of Arg72Pro polymorphism in P53 gene in cancer susceptibility in Algerian population
TP53 is a tumor suppressor gene involved in the development of several types of cancer. It has been reported that single nucleotide polymorphism in codon 72 of this gene, causing substitution of a Proline for an Arginine, may increase the risk of carcinogenesis. The objective of this study was to assess the frequency of the Arg72Pro polymorphism and to look for a possible association between this polymorphism and the occurrence of cancer. Our study concerned 82 DNA samples collected from the DNA bank of the Laboratory of Biology and Molecular Genetics of the Constantine University 3, and grouped 2 populations: 41 controls and 41 patients with one of three types of cancer: breast cancer, cervical cancer and lung cancer. This polymorphism was detected with PCR / RFLP. The results obtained in our study revealed a significant difference between the two patient and control groups for the heterozygous CG genotype (OR = 0.13, P = 0.001), which makes it possible to conclude that the CG genotype constitutes a risk factor in the occurrence cancer. However, the study showed that there is no difference between the Pro allele and the Arg allele in the patients compared to the controls (OR = 0.95, P = 0.87), which could rule out the possible association between the Arg72Pro polymorphism and the onset of cancer.