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 Radiation and Risk Pub Date : 2023-01-01 DOI:10.21870/0131-3878-2023-32-3-97-108
M.A. Yanishevskaya, E.A. Blinova, A.V. Korechenkova, A.V. Akleyev
{"title":"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","authors":"M.A. Yanishevskaya, E.A. Blinova, A.V. Korechenkova, A.V. Akleyev","doi":"10.21870/0131-3878-2023-32-3-97-108","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":55862,"journal":{"name":"Radiation and Risk","volume":"1151 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association between the rs1052133 polymorphism of the OGG1 gene and the risk of malignant neoplasms development in people chronically exposed to radiation\",\"authors\":\"M.A. Yanishevskaya, E.A. Blinova, A.V. Korechenkova, A.V. Akleyev\",\"doi\":\"10.21870/0131-3878-2023-32-3-97-108\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":55862,\"journal\":{\"name\":\"Radiation and Risk\",\"volume\":\"1151 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Radiation and Risk\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21870/0131-3878-2023-32-3-97-108\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Physics and Astronomy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiation and Risk","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21870/0131-3878-2023-32-3-97-108","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Physics and Astronomy","Score":null,"Total":0}
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。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
期刊最新文献
Dynamics of formation of absorbed doses in the blood of laboratory animals from alpha-emitting radionuclides with successive decays Contribution of foodstuffs contained radionuclides to formation of internal radiation doses received in areas Bryansk region affected by the Chernobyl accident Evaluation of permissible level of soluble I-131 containing fission products for design of protective measures in livestock industry Computed tomography as a risk factor of cancer among the population of the nuclear city of Ozyorsk Radiation-migration equivalence of radioactive waste and uranium raw materials in two-component nuclear power
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1