慢性辐射暴露人群中OGG1基因rs1052133多态性与恶性肿瘤发展风险之间的关系

Q4 Physics and Astronomy
M.A. Yanishevskaya, E.A. Blinova, A.V. Korechenkova, A.V. Akleyev
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引用次数: 0

摘要

遗传易感性无疑是癌症发生的危险因素之一。众所周知,维持基因组稳定性的基因的单核苷酸多态性(SNP),包括DNA修复的SNP,可能有助于癌变的开始。支持基因组稳定性的基因的单核苷酸多态性,包括DNA修复基因的SNP,可能有助于癌症的发生。切除修复基因OGG1的多态性引起了各国领先科学团体的兴趣。假设该基因rs1052133多态性与癌症发生易感性之间存在关系。本研究的目的是建立长期暴露于电离辐射人群中碱基切除修复基因OGG1 rs1052133多态性与癌症发生风险之间的关系。居住在特查河畔的居民(888人)长期受到来自特查河和东乌拉尔放射性痕迹的低或中辐射,他们被纳入了这项研究。该研究使研究人员确定,暴露于慢性辐射的人,携带rs1052133*G等位基因的人发生恶性肿瘤的风险增加:OR=1.38;95% CI [1.05 ~ 1.83], p=0.023。发现红骨髓剂量与OGG1基因rs1052133多态性之间存在多因子协同作用:测试平衡精度(TBA)=0.56;交叉验证一致性(CVC)=10/10;p = 0.01)。研究发现,rs1052133多态性可能被认为是长期暴露于剂量范围为0.74至3507.07 mGy(平均523.10+/-33.89 mGy)的辐射人群癌症发生风险的遗传标记。我们发现rs1052133*G的存在与辐射暴露可以改变实体癌发生的风险,SNP与辐射剂量之间存在协同关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between the rs1052133 polymorphism of the OGG1 gene and the risk of malignant neoplasms development in people chronically exposed to radiation
Genetic predisposition without doubt is one of the risk factors of cancer initiation. It is known that single nucleotide polymorphisms (SNP) of genes that maintain the genome stability, including SNP of DNA repair, may contribute to the initiation of carcinogenesis. Single-nucleotide polymorphisms of genes that support genome stability, including SNP of DNA repair genes, can contribute to cancer initiation. Polymorphism of the excision repair gene OGG1 causes interest of leading scientific groups from various countries. It is assumed that there is relationship between the rs1052133 polymorphism in the gene and predisposition to cancer initiation. The objective of this study was to establish association between rs1052133 polymorphism of base excision repair gene OGG1 and the risk of cancer initiation in people chronically exposed to ionizing radiation. Residents (888 people) of the Techa riverside settlements, chronically exposed to low or medium radiation from the Techa River and the East-Urals Radioactive Trace were included in the study. The study allowed researchers to establish that exposed to chronic radiation people, carriers of the rs1052133*G allele have increased risk of malignant neoplasms initiation: OR=1.38; 95% CI [1.05-1.83], p=0.023. The multifactorial synergistic interactions between the dose to the red bone marrow and the rs1052133 polymorphism of the OGG1 gene was found: Testing Balanced Accuracy (TBA)=0.56; Cross Validation Consistency (CVC)=10/10; p=0.01). The study found that the rs1052133 polymorphism may be considered as genetical marker of risk of cancer initiation in people, chronically exposed to radiation with doses ranged from 0.74 to 3507.07 mGy (average 523.10+/-33.89 mGy). It was found that the presence of the rs1052133*G in combination with radiation exposure can modify the risk of solid cancers initiation, as it is indicated by the synergistic relationship between the SNP and the radiation dose.
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来源期刊
Radiation and Risk
Radiation and Risk Physics and Astronomy-Nuclear and High Energy Physics
CiteScore
0.80
自引率
0.00%
发文量
27
期刊介绍: The Bulletin “Radiation and Risk” is a peer-reviewed scientific and practical periodical journal that covers many areas related to radiation effects on living systems. The journal publishes novel scientific papers related to the use of radiation in medicine, physics, epidemiology and biology, reviews, including scientific books reviews, as well as materials of the Russian Scientific Commission on Radiological Protection.
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