• 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

阿什肯纳兹犹太人群体中前列腺癌的遗传结构。

Genetic architecture of prostate cancer in the Ashkenazi Jewish population.

机构信息

Clinical Genetics Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Br J Cancer. 2011 Sep 6;105(6):864-9. doi: 10.1038/bjc.2011.307. Epub 2011 Aug 9.

DOI:10.1038/bjc.2011.307
PMID:21829199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3171013/
Abstract

BACKGROUND

Recently, numerous prostate cancer risk loci have been identified, some of which show association in specific populations. No study has yet investigated whether these single nucleotide polymorphisms (SNPs) are associated with prostate cancer in the Ashkenazi Jewish (AJ) population.

METHODS

A total of 29 known prostate cancer risk SNPs were genotyped in 963 prostate cancer cases and 613 controls of AJ ancestry. These data were combined with data from 1241 additional Ashkenazi controls and tested for association with prostate cancer. Correction for multiple testing was performed using the false discovery rate procedure.

RESULTS

Ten of twenty-three SNPs that passed quality control procedures were associated with prostate cancer risk at a false discovery rate of 5%. Of these, nine were originally discovered in studies of individuals of European ancestry. Based on power calculations, the number of significant associations observed is not surprising.

CONCLUSION

We see no convincing evidence that the genetic architecture of prostate cancer in the AJ population is substantively different from that observed in other populations of European ancestry.

摘要

背景

最近,许多前列腺癌风险基因座已被确定,其中一些在特定人群中表现出相关性。目前还没有研究调查这些单核苷酸多态性(SNP)是否与阿什肯纳兹犹太人(AJ)人群中的前列腺癌有关。

方法

对 963 例前列腺癌病例和 613 例 AJ 血统对照者的 29 个已知前列腺癌风险 SNP 进行了基因分型。这些数据与另外 1241 名阿什肯纳兹对照者的数据相结合,并进行了与前列腺癌的相关性检测。使用错误发现率程序对多重检测进行了校正。

结果

经过质量控制程序的 23 个 SNP 中有 10 个与前列腺癌风险相关,其假发现率为 5%。其中,有 9 个是在对欧洲血统个体的研究中首次发现的。根据功效计算,观察到的显著关联数量并不令人意外。

结论

我们没有发现令人信服的证据表明 AJ 人群中前列腺癌的遗传结构与其他欧洲血统人群中的遗传结构有实质性的不同。

相似文献

1
Genetic architecture of prostate cancer in the Ashkenazi Jewish population.阿什肯纳兹犹太人群体中前列腺癌的遗传结构。
Br J Cancer. 2011 Sep 6;105(6):864-9. doi: 10.1038/bjc.2011.307. Epub 2011 Aug 9.
2
Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry.Y 染色体单倍群与欧洲和阿什肯纳兹犹太人群体中的前列腺癌。
Hum Genet. 2012 Jul;131(7):1173-85. doi: 10.1007/s00439-012-1139-5. Epub 2012 Jan 24.
3
Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.与具有强烈家族史但无可识别 BRCA1/2 突变的阿什肯纳兹犹太裔女性乳腺癌风险相关的遗传变异。
Hum Genet. 2013 May;132(5):523-36. doi: 10.1007/s00439-013-1269-4. Epub 2013 Jan 25.
4
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.全基因组关联研究鉴定出一个阿什肯纳兹犹太人群体中的帕金森病候选基因。
BMC Med Genet. 2011 Aug 3;12:104. doi: 10.1186/1471-2350-12-104.
5
Breast cancer polygenic risk scores derived in White European populations are not calibrated for women of Ashkenazi Jewish descent.白人欧洲人群中得出的乳腺癌多基因风险评分不适用于阿什肯纳兹犹太血统的女性。
Genet Med. 2023 Sep;25(9):100846. doi: 10.1016/j.gim.2023.100846. Epub 2023 Apr 12.
6
A genetic study and meta-analysis of the genetic predisposition of prostate cancer in a Chinese population.一项针对中国人群前列腺癌遗传易感性的基因研究与荟萃分析。
Oncotarget. 2016 Apr 19;7(16):21393-403. doi: 10.18632/oncotarget.7250.
7
Mitochondrial DNA Haplogroup K Is Protective Against Autism Spectrum Disorder Risk in Populations of European Ancestry.线粒体 DNA 单倍群 K 可降低欧洲人群自闭症谱系障碍风险。
J Am Acad Child Adolesc Psychiatry. 2024 Aug;63(8):835-844. doi: 10.1016/j.jaac.2023.09.550. Epub 2023 Dec 8.
8
Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer.阿什肯纳兹犹太裔前列腺癌男性中 CHEK2 基因新型单核苷酸多态性的鉴定与表征
Cancer Lett. 2008 Oct 18;270(1):173-80. doi: 10.1016/j.canlet.2008.05.006. Epub 2008 Jun 20.
9
Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population.阿什肯纳兹犹太人群中的2型糖尿病易感基因座。
Hum Genet. 2008 Aug;124(1):101-4. doi: 10.1007/s00439-008-0520-x. Epub 2008 May 31.
10
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population.阿什肯纳兹犹太人遗传特征与健康和疾病的关联。
Genome Biol. 2012 Jan 25;13(1):R2. doi: 10.1186/gb-2012-13-1-r2.

引用本文的文献

1
SNPs at SMG7 Associated with Time from Biochemical Recurrence to Prostate Cancer Death.SMG7基因单核苷酸多态性与前列腺癌生化复发至死亡的时间相关。
Cancer Epidemiol Biomarkers Prev. 2022 Jul 1;31(7):1466-1472. doi: 10.1158/1055-9965.EPI-22-0053.
2
PRNCR1: a long non-coding RNA with a pivotal oncogenic role in cancer.PRNCR1:一种长非编码 RNA,在癌症中具有关键致癌作用。
Hum Genet. 2022 Jan;141(1):15-29. doi: 10.1007/s00439-021-02396-8. Epub 2021 Nov 2.
3
Clinical correlations and prognostic value of Nudix hydroxylase 10 in patients with gastric cancer.胃癌患者 Nudix 水解酶 10 的临床相关性及其预后价值。
Bioengineered. 2021 Dec;12(2):9779-9789. doi: 10.1080/21655979.2021.1995104.
4
Validation of prostate cancer risk variants rs10993994 and rs7098889 by CRISPR/Cas9 mediated genome editing.利用 CRISPR/Cas9 介导的基因组编辑技术验证前列腺癌风险变异 rs10993994 和 rs7098889。
Gene. 2021 Feb 5;768:145265. doi: 10.1016/j.gene.2020.145265. Epub 2020 Oct 26.
5
Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma.琥珀酸脱氢酶 FH c.1431_1433dupAAA(p.Lys477dup) 变异与癌症(包括肾细胞癌)无关。
Hum Mutat. 2020 Jan;41(1):103-109. doi: 10.1002/humu.23900. Epub 2019 Sep 3.
6
NUDT11 rs5945572 polymorphism and prostate cancer risk: a meta-analysis.NUDT11基因rs5945572多态性与前列腺癌风险:一项荟萃分析。
Int J Clin Exp Med. 2015 Mar 15;8(3):3474-81. eCollection 2015.
7
A genome-wide association study of prostate cancer in West African men.泛非男性前列腺癌的全基因组关联研究。
Hum Genet. 2014 May;133(5):509-21. doi: 10.1007/s00439-013-1387-z. Epub 2013 Nov 2.
8
Variants at IRX4 as prostate cancer expression quantitative trait loci.IRX4基因变异作为前列腺癌表达数量性状位点
Eur J Hum Genet. 2014 Apr;22(4):558-63. doi: 10.1038/ejhg.2013.195. Epub 2013 Sep 11.
9
Characterization of SNPs associated with prostate cancer in men of Ashkenazic descent from the set of GWAS identified SNPs: impact of cancer family history and cumulative SNP risk prediction.鉴定全基因组关联研究 SNPs 中与阿什肯纳兹裔男性前列腺癌相关的单核苷酸多态性的特征:家族癌症史的影响和累积 SNP 风险预测。
PLoS One. 2013;8(4):e60083. doi: 10.1371/journal.pone.0060083. Epub 2013 Apr 3.

本文引用的文献

1
Prostate cancer risk-associated variants reported from genome-wide association studies: meta-analysis and their contribution to genetic Variation.全基因组关联研究中报道的前列腺癌风险相关变异:荟萃分析及其对遗传变异的贡献。
Prostate. 2010 Dec 1;70(16):1729-38. doi: 10.1002/pros.21208.
2
Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.精确定位 7p15.2 染色体上 JAZF1 基因中的前列腺癌遗传关联。
Cancer Epidemiol Biomarkers Prev. 2010 May;19(5):1349-55. doi: 10.1158/1055-9965.EPI-09-1181. Epub 2010 Apr 20.
3
Replication of prostate cancer risk loci on 8q24, 11q13, 17q12, 19q33, and Xp11 in African Americans.非洲裔美国人中前列腺癌风险基因座 8q24、11q13、17q12、19q33 和 Xp11 的复制。
Prostate. 2010 Feb 15;70(3):270-5. doi: 10.1002/pros.21061.
4
Association of 17 prostate cancer susceptibility loci with prostate cancer risk in Chinese men.17 个前列腺癌易感性位点与中国男性前列腺癌风险的关联。
Prostate. 2010 Mar 1;70(4):425-32. doi: 10.1002/pros.21076.
5
Identification of a new prostate cancer susceptibility locus on chromosome 8q24.在8号染色体q24区域鉴定出一个新的前列腺癌易感基因座。
Nat Genet. 2009 Oct;41(10):1055-7. doi: 10.1038/ng.444. Epub 2009 Sep 20.
6
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.全基因组关联研究和重复研究确定了与前列腺癌易感性相关的四个变异。
Nat Genet. 2009 Oct;41(10):1122-6. doi: 10.1038/ng.448. Epub 2009 Sep 20.
7
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.通过全基因组关联研究鉴定出七个新的前列腺癌易感基因座。
Nat Genet. 2009 Oct;41(10):1116-21. doi: 10.1038/ng.450. Epub 2009 Sep 20.
8
Replication of prostate cancer risk loci in a Japanese case-control association study.日本病例对照关联研究中前列腺癌风险位点的复制
J Natl Cancer Inst. 2009 Oct 7;101(19):1330-6. doi: 10.1093/jnci/djp287. Epub 2009 Sep 2.
9
Generalizability of associations from prostate cancer genome-wide association studies in multiple populations.多人群前列腺癌全基因组关联研究中关联的可推广性。
Cancer Epidemiol Biomarkers Prev. 2009 Apr;18(4):1285-9. doi: 10.1158/1055-9965.EPI-08-1142. Epub 2009 Mar 24.
10
Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer.阿什肯纳兹犹太裔前列腺癌男性中 CHEK2 基因新型单核苷酸多态性的鉴定与表征
Cancer Lett. 2008 Oct 18;270(1):173-80. doi: 10.1016/j.canlet.2008.05.006. Epub 2008 Jun 20.