• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

中国宣威地区DNA碱基切除修复基因APEX1和XRCC1的多态性与肺癌风险

Polymorphisms in the DNA base excision repair genes APEX1 and XRCC1 and lung cancer risk in Xuan Wei, China.

作者信息

Shen Min, Berndt Sonja I, Rothman Nathaniel, Mumford Judy L, He Xingzhou, Yeager Meredith, Welch Robert, Chanock Stephen, Keohavong Phouthone, Donahue Mark, Zheng Tongzhang, Caporaso Neil, Lan Qing

机构信息

Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, Maryland 20892-7240, USA.

出版信息

Anticancer Res. 2005 Jan-Feb;25(1B):537-42.

PMID:15816625
Abstract

The lung cancer mortality rate in Xuan Wei is among the highest in China and has been causally attributed to high exposure to indoor smoky coal emissions, which contain high levels of PAHs and can lead to modified bases. We studied genetic polymorphisms in four DNA base excision repair genes in a population-based case-control study in Xuan Wei with 122 lung cancer cases and 122 controls. Homozygous carriers of the APEX1 148Glu variant had an increased risk (OR, 2.13; 95% CI, 0.96-4.74), whereas persons with the XRCC1 399Gln allele had a decreased risk (OR, 0.60; 95% CI, 0.35-1.02) of lung cancer compared with wild-type carriers. Subjects with both at-risk genotypes (APEX1 Glu148Glu and XRCC1 Arg399Arg) had a higher risk of lung cancer (OR: 3.34; 95% CI: 1.16-9.67). We found genetic variants in APEX1 and XRCC1 may alter the risk of lung cancer in a special population in China.

摘要

宣威的肺癌死亡率位居中国前列,其病因被认为是长期暴露于室内煤烟排放物中,这些排放物含有高浓度的多环芳烃,并可导致碱基修饰。我们在宣威进行了一项基于人群的病例对照研究,对122例肺癌病例和122例对照者的四个DNA碱基切除修复基因的遗传多态性进行了研究。携带APEX1 148Glu变异的纯合子患癌风险增加(比值比,2.13;95%置信区间,0.96 - 4.74),而携带XRCC1 399Gln等位基因的人患肺癌的风险低于野生型携带者(比值比,0.60;95%置信区间,0.35 - 1.02)。同时具有两种风险基因型(APEX1 Glu148Glu和XRCC1 Arg399Arg)的受试者患肺癌的风险更高(比值比:3.34;95%置信区间:1.16 - 9.67)。我们发现APEX1和XRCC1中的基因变异可能会改变中国某一特定人群的肺癌风险。

相似文献

1
Polymorphisms in the DNA base excision repair genes APEX1 and XRCC1 and lung cancer risk in Xuan Wei, China.中国宣威地区DNA碱基切除修复基因APEX1和XRCC1的多态性与肺癌风险
Anticancer Res. 2005 Jan-Feb;25(1B):537-42.
2
Polymorphisms in the DNA repair genes XRCC1, APEX1, XRCC3 and NBS1, and the risk for lung cancer in never- and ever-smokers.DNA修复基因XRCC1、APEX1、XRCC3和NBS1的多态性与从不吸烟者和曾经吸烟者患肺癌的风险
Lung Cancer. 2006 Dec;54(3):285-92. doi: 10.1016/j.lungcan.2006.08.004. Epub 2006 Oct 10.
3
Gene-environment interactions between the smoking habit and polymorphisms in the DNA repair genes, APE1 Asp148Glu and XRCC1 Arg399Gln, in Japanese lung cancer risk.吸烟习惯与DNA修复基因APE1 Asp148Glu和XRCC1 Arg399Gln多态性之间的基因-环境相互作用对日本肺癌风险的影响。
Carcinogenesis. 2004 Aug;25(8):1395-401. doi: 10.1093/carcin/bgh153. Epub 2004 Mar 25.
4
Polymorphisms in three base excision repair genes and breast cancer risk in Thai women.泰国女性中三个碱基切除修复基因的多态性与乳腺癌风险
Breast Cancer Res Treat. 2008 Sep;111(2):279-88. doi: 10.1007/s10549-007-9773-7. Epub 2007 Oct 6.
5
Genetic polymorphisms in the base excision repair pathway and cancer risk: a HuGE review.碱基切除修复途径中的基因多态性与癌症风险:一项HuGE综述
Am J Epidemiol. 2005 Nov 15;162(10):925-42. doi: 10.1093/aje/kwi318. Epub 2005 Oct 12.
6
Specific combinations of DNA repair gene variants and increased risk for non-small cell lung cancer.DNA修复基因变异的特定组合与非小细胞肺癌风险增加
Carcinogenesis. 2004 Dec;25(12):2433-41. doi: 10.1093/carcin/bgh264. Epub 2004 Aug 27.
7
Indoor coal combustion emissions, GSTM1 and GSTT1 genotypes, and lung cancer risk: a case-control study in Xuan Wei, China.室内燃煤排放、谷胱甘肽S-转移酶M1和T1基因型与肺癌风险:中国宣威的一项病例对照研究
Cancer Epidemiol Biomarkers Prev. 2000 Jun;9(6):605-8.
8
Polymorphisms in folate metabolic genes and lung cancer risk in Xuan Wei, China.中国宣威地区叶酸代谢基因多态性与肺癌风险
Lung Cancer. 2005 Sep;49(3):299-309. doi: 10.1016/j.lungcan.2005.04.002.
9
Polymorphisms in base-excision repair and nucleotide-excision repair genes in relation to lung cancer risk.碱基切除修复和核苷酸切除修复基因多态性与肺癌风险的关系。
Mutat Res. 2007 Jul 28;631(2):101-10. doi: 10.1016/j.mrgentox.2007.03.010. Epub 2007 Apr 21.
10
Polymorphisms in DNA base excision repair genes ADPRT and XRCC1 and risk of lung cancer.DNA碱基切除修复基因ADPRT和XRCC1的多态性与肺癌风险
Cancer Res. 2005 Feb 1;65(3):722-6.

引用本文的文献

1
Associations between polymorphisms in genes of base excision repair pathway and lung cancer risk.碱基切除修复途径基因多态性与肺癌风险之间的关联。
Transl Cancer Res. 2020 Apr;9(4):2780-2800. doi: 10.21037/tcr.2020.02.44.
2
Modulation of Colorectal Cancer Risk by Polymorphisms in 51Gln/His, 64Ile/Val, and 148Asp/Glu of APEX Gene; 23Gly/Ala of XPA Gene; and 689Ser/Arg of ERCC4 Gene.APEX基因51Gln/His、64Ile/Val和148Asp/Glu多态性;XPA基因23Gly/Ala多态性;以及ERCC4基因689Ser/Arg多态性对结直肠癌风险的调节作用
Gastroenterol Res Pract. 2017;2017:3840243. doi: 10.1155/2017/3840243. Epub 2017 Mar 12.
3
RRM1 *151A>T, RRM1 -756T>C, and RRM1 -585T>Gis associated with increased susceptibility of lung cancer in Chinese patients.
RRM1基因151位密码子A突变为T、RRM1基因-756位T突变为C以及RRM1基因-585位T突变为G与中国肺癌患者易感性增加相关。
Cancer Med. 2016 Aug;5(8):2084-90. doi: 10.1002/cam4.703. Epub 2016 Jun 23.
4
Genetic Polymorphisms of X-ray Repair Cross-Complementing Group 1 and Apurinic/Apyrimidinic Endonuclease-1 in Chronic Obstructive Pulmonary Disease.慢性阻塞性肺疾病中X射线修复交叉互补基因1和脱嘌呤/脱嘧啶内切酶1的基因多态性
Inflammation. 2016 Jun;39(3):1198-204. doi: 10.1007/s10753-016-0355-x.
5
The relationship between altered mitochondrial DNA copy number and cancer risk: a meta-analysis.线粒体DNA拷贝数改变与癌症风险之间的关系:一项荟萃分析。
Sci Rep. 2015 May 8;5:10039. doi: 10.1038/srep10039.
6
Note of clarification of data in the paper titled X-ray repair cross-complementing group 1 codon 399 polymorphism and lung cancer risk: an updated meta-analysis.关于题为《X射线修复交叉互补基因1第399位密码子多态性与肺癌风险:一项更新的荟萃分析》的论文中数据的澄清说明
Tumour Biol. 2015 May;36(5):3179-89. doi: 10.1007/s13277-015-3384-4. Epub 2015 Apr 3.
7
Note of clarification of data in the paper entitled no association between XRCC1 gene Arg194Trp polymorphism and risk of lung cancer: evidence based on an updated cumulative meta-analysis.题为《XRCC1基因Arg194Trp多态性与肺癌风险无关联:基于更新的累积荟萃分析的证据》的论文中数据的澄清说明
Tumour Biol. 2015 Apr;36(4):2235-40. doi: 10.1007/s13277-015-3234-4. Epub 2015 Mar 14.
8
Note of clarification of data in the paper titled X-ray repair cross-complementing group 1 Arg194Trp polymorphism is associated with increased risk of lung cancer in Chinese Han population.关于题为《X射线修复交叉互补基因1的Arg194Trp多态性与中国汉族人群肺癌风险增加相关》论文中数据的澄清说明
Tumour Biol. 2015 Apr;36(4):2229-33. doi: 10.1007/s13277-015-3201-0. Epub 2015 Feb 11.
9
Evaluating the association of polymorphisms in the HAP1 gene with lung cancer risk: a meta-analysis.评估HAP1基因多态性与肺癌风险的关联:一项荟萃分析。
Tumour Biol. 2014 Nov;35(11):10825-31. doi: 10.1007/s13277-014-2236-y. Epub 2014 Aug 1.
10
Association between the XRCC1 Arg194Trp polymorphism and risk of cancer: evidence from 201 case-control studies.XRCC1基因Arg194Trp多态性与癌症风险的关联:来自201项病例对照研究的证据。
Tumour Biol. 2014 Nov;35(11):10677-97. doi: 10.1007/s13277-014-2326-x. Epub 2014 Jul 27.