期刊文献+

DNA修复基因XPC多态性与乳腺癌易感性关系的Meta分析

Meta Analysis of Association Between Polymorphism of XPC and Susceptibility of Breast Cancer
下载PDF
导出
摘要 目的利用Meta分析探讨DNA修复基因着色性干皮病基因组C(XPC)Ala499Val多态性与乳腺癌易感性的关系。方法通过Pub Med、Embase、Web of Science和中国生物医学文献数据库,检索XPC基因多态性与乳腺癌易感性相关的文献。由2位研究者独立筛选文献并提取相关数据资料,采用STATA 12.0软件进行Meta分析。结果按照纳入标准,最终纳入Meta分析的研究有9项。Meta分析结果显示:XPC Ala499Val在纯合子模型[(Val/Val)vs(Ala/Ala)]和隐性模型[(Val/Val)vs(Ala/Val+Ala/Ala)]下与乳腺癌易感性之间存在相关性(纯合子模型:OR=1.21,95%CI:1.02~1.45;隐性模型:OR=1.23,95%CI:1.05~1.43)。结论 XPC Ala499Val多态性与乳腺癌易感性之间存在相关,但上述结论尚需要大样本量的研究予以验证。 Objective To study the association between xeroderma pigmentosum group C(XPC) Ala499 Val polymorphism and susceptibility of breast cancer by meta-analysis.Methods Literatures were searched from Pub Med,Embase,Web of Science and Chinese Biomedical Literature databases.The literatures were independently screened by two investigators,and Meta analysis was performed by using STATA 12.0 software.Results A total of 9 studies were included in the final Meta analysis according to the inclusion criteria.The results of Meta analysis showed that,XPC Ala499 Val was associated with increased susceptibility of breast cancer under the homozygous model(OR=1.21,95% CI:1.02-1.45) and the recessive model(OR=1.23,95% CI:1.05-1.43).Conclusion XPC Ala499 Val polymorphism may contribute to the breast cancer risk,which needs further validation in single large studies.
出处 《肿瘤基础与临床》 2017年第5期424-426,共3页 journal of basic and clinical oncology
关键词 DNA修复基因 着色性干皮病基因组C 单核苷酸多态性 乳腺癌 META分析 DNA repair gene xeroderma pigmentosum group C single nucleotide polymorphism breast cancer Meta analysis
  • 相关文献

参考文献2

二级参考文献18

  • 1Bonito MD, Cantile M, Malzone G, et al. The prognostic role of cancer stem cells in breast tumors [ J]. J Clin Med Res, 2013,5 (5) :325 -326.
  • 2McClements L, Yakkundi A, Papaspyropoulos A, et al. Targeting treatment-resistant breast cancer stem cells with FKBPL and its peptide derivative, AD-O1, via the CIM4 pathway[ J]. Clin Cancer Res ,2013,19 (14) :3881 - 3893.
  • 3T. J. Jorgensen,K. Visvanathan,I. Ruczinski,L. Thuita,S. Hoffman,K. J. Helzlsouer.Breast Cancer Risk is not Associated with Polymorphic Forms of Xeroderma Pigmentosum Genes in a Cohort of Women from Washington County, Maryland[J]. Breast Cancer Research and Treatment . 2007 (1)
  • 4LEE G Y,JANG J S,LEE S Y,et al.XPCpolymorphisms and lung cancer risk. International Journal of Cancer . 2005
  • 5HIRATA H,,HINODA Y,TANAKA Y,et al.Polymorphisms of DNA repair genes are risk factorsfor prostate cancer. European Journal of Cancer . 2007
  • 6PAN J,LINJ,IZZO J G,et al.Genetic susceptibilityto esophageal cancer:the role of the nucleotideexcision repair pathway. Carcinogenesis . 2009
  • 7YANG Z H,LIANG W B,JIA J,et al.Thexeroderma pigmentosum group C genepolymorphisms and genetic susceptibility ofnasopharyngeal carcinoma. Acta Oncologica(Stockholm,Sweden) . 2008
  • 8Smith TR,Levine EA,Freimanis RI. et al.Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk. Carcinogenesis . 2008
  • 9Spek P.J,Smit E.M,Beverloo H.B,et al.Chromosomal localization of three repair genes; the xeroderma pigmentosum group C gene and two human homologs of yeast RAD23. Genomics . 1994
  • 10L Zhang,Z Zhang,W Yan.Single nucleotide polymorphisms for DNA repair genes in breast cancer patients. Clinica Chimica Acta . 2005

共引文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部