• 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

TNRC9基因的单核苷酸多态性与中国汉族女性乳腺癌风险相关。

A single nucleotide polymorphism of the TNRC9 gene associated with breast cancer risk in Chinese Han women.

作者信息

Chen F, Zhou J, Xue Y, Yang S, Xiong M, Li Y, Liu Q

机构信息

Life Sciences School of Hubei University, Wuchang, Wuhan, China.

Wuhan Tuberculosis Dispensary, Qiaokou, Wuhan, China.

出版信息

Genet Mol Res. 2014 Jan 10;13(1):182-7. doi: 10.4238/2014.January.10.9.

DOI:10.4238/2014.January.10.9
PMID:24446301
Abstract

A single nucleotide polymorphism (SNP) in the TNRC9 gene was identified as a breast cancer susceptibility genetic variant in recent genome-wide association studies of women of European ancestry. We investigated whether TNRC9 polymorphisms are associated with risk of breast cancer in Chinese women of the Han nationality. We genotyped the SNPs rs3803662, rs1362548, rs1123428 in 870 women, including 388 breast cancer patients and 482 healthy controls, via the PCR-single strand conformation polymorphism procedure and by sequence detection. We found that the T allele and the TT genotype of the SNP rs38033662 is significantly associated with risk for breast cancer in Chinese Han women; however, no significant association was found for rs1362548 or rs1123428. We conclude that SNP rs3803662 is a putative risk factor for breast cancer in Chinese Han women.

摘要

在最近针对欧洲血统女性的全基因组关联研究中,TNRC9基因中的一个单核苷酸多态性(SNP)被确定为乳腺癌易感性基因变异。我们调查了TNRC9基因多态性是否与中国汉族女性的乳腺癌风险相关。我们通过聚合酶链反应-单链构象多态性方法和序列检测,对870名女性(包括388例乳腺癌患者和482名健康对照)的SNP rs3803662、rs1362548、rs1123428进行基因分型。我们发现,SNP rs38033662的T等位基因和TT基因型与中国汉族女性的乳腺癌风险显著相关;然而,rs1362548或rs1123428未发现显著相关性。我们得出结论,SNP rs3803662是中国汉族女性乳腺癌的一个假定风险因素。

相似文献

1
A single nucleotide polymorphism of the TNRC9 gene associated with breast cancer risk in Chinese Han women.TNRC9基因的单核苷酸多态性与中国汉族女性乳腺癌风险相关。
Genet Mol Res. 2014 Jan 10;13(1):182-7. doi: 10.4238/2014.January.10.9.
2
Relationship between five GWAS-identified single nucleotide polymorphisms and female breast cancer in the Chinese Han population.中国汉族人群中5个全基因组关联研究鉴定的单核苷酸多态性与女性乳腺癌的关系。
Tumour Biol. 2016 Jul;37(7):9739-44. doi: 10.1007/s13277-016-4795-6. Epub 2016 Jan 23.
3
Genetic variants in FGFR2 and TNRC9 genes are associated with breast cancer risk in Pakistani women.FGFR2和TNRC9基因中的遗传变异与巴基斯坦女性患乳腺癌的风险相关。
Mol Med Rep. 2016 Oct;14(4):3443-51. doi: 10.3892/mmr.2016.5633. Epub 2016 Aug 18.
4
Association between polymorphisms of trinucleotide repeat containing 9 gene and breast cancer risk: evidence from 62,005 subjects.三核苷酸重复序列 9 基因多态性与乳腺癌风险的关联:来自 62005 名受试者的证据。
Breast Cancer Res Treat. 2011 Feb;126(1):177-83. doi: 10.1007/s10549-010-1114-6. Epub 2010 Aug 12.
5
Genetic variants in trinucleotide repeat-containing 9 (TNRC9) are associated with risk of estrogen receptor positive breast cancer in a Chinese population.三核苷酸重复序列含 9 号基因(TNRC9)中的遗传变异与中国人群雌激素受体阳性乳腺癌的风险相关。
Breast Cancer Res Treat. 2010 Nov;124(1):237-41. doi: 10.1007/s10549-010-0809-z. Epub 2010 Mar 9.
6
TNRC9 rs12443621 and FGFR2 rs2981582 polymorphisms and breast cancer risk.TNRC9基因rs12443621位点和FGFR2基因rs2981582位点多态性与乳腺癌风险
World J Surg Oncol. 2016 Feb 24;14(1):50. doi: 10.1186/s12957-016-0795-7.
7
Significant association of TOX3/LOC643714 locus-rs3803662 and breast cancer risk in a cohort of Iranian population.TOX3/LOC643714 基因座-rs3803662 与伊朗人群乳腺癌风险的显著相关性。
Mol Biol Rep. 2019 Feb;46(1):805-811. doi: 10.1007/s11033-018-4535-7. Epub 2018 Dec 4.
8
Two polymorphisms, rs2046210 and rs3803662, are associated with breast cancer risk in a Vietnamese case-control cohort.在一个越南病例对照队列中,两种多态性,即rs2046210和rs3803662,与乳腺癌风险相关。
Genes Genet Syst. 2018 Oct 30;93(3):101-109. doi: 10.1266/ggs.17-00053. Epub 2018 Aug 6.
9
Common genetic variants associated with breast cancer in Korean women and differential susceptibility according to intrinsic subtype.与韩国女性乳腺癌相关的常见遗传变异及其根据内在亚型的差异易感性。
Cancer Epidemiol Biomarkers Prev. 2011 May;20(5):793-8. doi: 10.1158/1055-9965.EPI-10-1282. Epub 2011 Mar 17.
10
[Associations between TOX3 rs3803662 polymorphisms and immunological markers of breast cancer].[TOX3基因rs3803662多态性与乳腺癌免疫标志物之间的关联]
Zhonghua Yi Xue Za Zhi. 2015 Sep 8;95(34):2783-6.

引用本文的文献

1
Study of Single Nucleotide Polymorphisms Associated with Breast Cancer Patients among Arab Ancestries.阿拉伯裔乳腺癌患者相关单核苷酸多态性研究。
Int J Breast Cancer. 2022 Oct 11;2022:2442109. doi: 10.1155/2022/2442109. eCollection 2022.
2
Association between the TOX3 rs3803662 C>T polymorphism and recurrent miscarriage in a southern Chinese population.TOX3 rs3803662 C>T 多态性与中国南方人群复发性流产的相关性研究。
J Clin Lab Anal. 2019 Nov;33(9):e22992. doi: 10.1002/jcla.22992. Epub 2019 Aug 27.
3
CTLA-4 Genetic Variants (rs11571317 and rs3087243): Role in Susceptibility and Progression of Breast Cancer.
细胞毒性T淋巴细胞相关抗原4基因变体(rs11571317和rs3087243):在乳腺癌易感性和进展中的作用
World J Oncol. 2017 Oct;8(5):162-170. doi: 10.14740/wjon1046w. Epub 2017 Nov 5.
4
Association of single nucleotide polymorphism rs3803662 with the risk of breast cancer.单核苷酸多态性 rs3803662 与乳腺癌风险的关联。
Sci Rep. 2016 Jun 28;6:29008. doi: 10.1038/srep29008.