• 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

rs1447295基因多态性与前列腺癌易感性关联的Meta分析。

Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility.

作者信息

Zhou Juan, Yu Yang, Zhu Anyou, Wang Fengchao, Kang Shuxia, Pei Yunfeng, Cao Chunping, Ding Chen, Wang Duping, Sun Li, Niu Guoping

机构信息

Department of Clinical Laboratory, Affiliated to Medical College of Southeast University and Xuzhou Central Hospital, Xuzhou, People's Republic of China.

Department of Medical Oncology, Affiliated to Medical College of Southeast University and Xuzhou Central Hospital, Xuzhou, People's Republic of China.

出版信息

Oncotarget. 2017 May 5;8(40):67029-67042. doi: 10.18632/oncotarget.17627. eCollection 2017 Sep 15.

DOI:10.18632/oncotarget.17627
PMID:28978014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5620154/
Abstract

AIMS

A number of studies have found that the single nucleotide polymorphisms (SNPs) within the 8q24 region of genome were associated with the susceptibility of prostate cancer. Association between 8q24 SNP variant rs1447295 and higher risk of prostate cancer had been investigated, but those studies were incomplete and the conclusions were obscure.

METHODS

To better elucidate the relationship between rs1447295 polymorphism and the susceptibility of prostate cancer, we performed a more comprehensive meta-analysis about the association between rs1447295 polymorphism and prostate cancer susceptibility by collecting relevant articles published up to November, 2016 and excluding many replicated cohort data existing in previous reports, which made the conclusion more reliant and objective.

RESULTS

The results showed that there was a significant prostate cancer risk associated with rs1447295 polymorphism not only in the total groups, but also in American, European and Asian descent subgroups. Meanwhile, a comprehensive analysis about the association between rs1447295 polymorphism and prostate cancer risk were conducted by using different clinical characteristic stratifications including Gleason score, tumor stage and PSA level. The result showed that rs1447295 polymorphism was correlated with different stages of prostate cancer.

CONCLUSIONS

There are strong association between rs1447295 polymorphism and prostate cancer susceptibility in different ethnic groups and different prostate cancer stage, suggesting that rs1447295 might serve as a reliable biomarker for prostate cancer diagnosis.

摘要

目的

多项研究发现,基因组8q24区域内的单核苷酸多态性(SNP)与前列腺癌易感性相关。已对8q24 SNP变异体rs1447295与前列腺癌高风险之间的关联进行了研究,但这些研究并不完整,结论也不明确。

方法

为了更好地阐明rs1447295多态性与前列腺癌易感性之间的关系,我们通过收集截至2016年11月发表的相关文章,并排除先前报告中存在的许多重复队列数据,对rs1447295多态性与前列腺癌易感性之间的关联进行了更全面的荟萃分析,这使得结论更具可靠性和客观性。

结果

结果表明,rs1447295多态性不仅在总体组中,而且在美国、欧洲和亚洲血统亚组中均与前列腺癌风险显著相关。同时,利用包括Gleason评分、肿瘤分期和PSA水平在内的不同临床特征分层,对rs1447295多态性与前列腺癌风险之间的关联进行了综合分析。结果表明,rs1447295多态性与前列腺癌的不同分期相关。

结论

rs1447295多态性与不同种族和不同前列腺癌分期的前列腺癌易感性之间存在密切关联,提示rs1447295可能作为前列腺癌诊断的可靠生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/f41505372c7c/oncotarget-08-67029-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/580661c62c94/oncotarget-08-67029-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/e6ea3f0a48e3/oncotarget-08-67029-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/bcf9e8fede82/oncotarget-08-67029-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/f5ebf9846453/oncotarget-08-67029-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/6b63342b24d0/oncotarget-08-67029-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/1731486b9c74/oncotarget-08-67029-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/82d3042b6aef/oncotarget-08-67029-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/71418cf2cfba/oncotarget-08-67029-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/f41505372c7c/oncotarget-08-67029-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/580661c62c94/oncotarget-08-67029-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/e6ea3f0a48e3/oncotarget-08-67029-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/bcf9e8fede82/oncotarget-08-67029-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/f5ebf9846453/oncotarget-08-67029-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/6b63342b24d0/oncotarget-08-67029-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/1731486b9c74/oncotarget-08-67029-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/82d3042b6aef/oncotarget-08-67029-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/71418cf2cfba/oncotarget-08-67029-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f41b/5620154/f41505372c7c/oncotarget-08-67029-g009.jpg

相似文献

1
Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility.rs1447295基因多态性与前列腺癌易感性关联的Meta分析。
Oncotarget. 2017 May 5;8(40):67029-67042. doi: 10.18632/oncotarget.17627. eCollection 2017 Sep 15.
2
The rs1447295 and DG8S737 markers on chromosome 8q24 and cancer risk in the Polish population.8q24 染色体上的 rs1447295 和 DG8S737 标记与波兰人群的癌症风险。
Eur J Cancer Prev. 2010 Mar;19(2):167-71. doi: 10.1097/CEJ.0b013e32832945c3.
3
The rs1447295 at 8q24 is a risk variant for prostate cancer in Taiwanese men.位于8号染色体长臂24区的rs1447295是台湾男性前列腺癌的一个风险变异位点。
Urology. 2009 Sep;74(3):698-701. doi: 10.1016/j.urology.2009.02.035. Epub 2009 May 9.
4
The common variant rs1447295 on chromosome 8q24 and prostate cancer risk: results from an Australian population-based case-control study.8号染色体q24区域的常见变异rs1447295与前列腺癌风险:一项基于澳大利亚人群的病例对照研究结果
Cancer Epidemiol Biomarkers Prev. 2007 Mar;16(3):610-2. doi: 10.1158/1055-9965.EPI-06-0872.
5
[Association of chromosome 8q24 variants with prostate cancer risk in the Siberian region of Russia and meta-analysis].[俄罗斯西伯利亚地区8号染色体q24变异与前列腺癌风险的关联及荟萃分析]
Mol Biol (Mosk). 2012 Mar-Apr;46(2):234-41.
6
A replication study examining association of rs6983267, rs10090154, and rs1447295 common single nucleotide polymorphisms in 8q24 region with prostate cancer in Siberians.一项在西伯利亚人群中,针对 8q24 区域中 rs6983267、rs10090154 和 rs1447295 常见单核苷酸多态性与前列腺癌关联性的复制研究。
Urol Oncol. 2014 Jan;32(1):37.e7-12. doi: 10.1016/j.urolonc.2013.02.017. Epub 2013 Apr 28.
7
Association of chromosomal locus 8q24 and risk of prostate cancer: a hospital-based study of German patients treated with brachytherapy.染色体位点8q24与前列腺癌风险的关联:一项基于医院的德国近距离放射治疗患者研究。
Urol Oncol. 2009 Jul-Aug;27(4):373-6. doi: 10.1016/j.urolonc.2008.04.010. Epub 2008 Jul 14.
8
Genetic variations at 8q24 and gastric cancer susceptibility: A meta-analysis study.8q24基因变异与胃癌易感性:一项荟萃分析研究。
PLoS One. 2017 Dec 12;12(12):e0188774. doi: 10.1371/journal.pone.0188774. eCollection 2017.
9
Association of SNP rs1447295 and microsatellite marker DG8S737 with familial prostate cancer and high grade disease.SNP rs1447295 与微卫星标记 DG8S737 与家族性前列腺癌和高级别疾病的关联。
J Urol. 2010 Aug;184(2):738-42. doi: 10.1016/j.juro.2010.03.102. Epub 2010 Jun 19.
10
Risk loci on chromosome 8q24 are associated with prostate cancer in northern Chinese men.8 号染色体 q24 上的风险位点与中国北方男性的前列腺癌有关。
J Urol. 2012 Jan;187(1):315-21. doi: 10.1016/j.juro.2011.09.011. Epub 2011 Nov 17.

引用本文的文献

1
Association between genetic variations at 8q24 and prostate cancer risk in Mexican Men.8q24 基因变异与墨西哥男性前列腺癌风险的关联。
Prostate Cancer Prostatic Dis. 2022 Sep;25(3):507-512. doi: 10.1038/s41391-021-00461-x. Epub 2021 Oct 1.
2
The association of polymorphisms in lncRNA- with hepatocellular cancer risk and prognosis.长非编码 RNA- 多态性与肝细胞癌风险和预后的关联。
Biosci Rep. 2018 Sep 5;38(5). doi: 10.1042/BSR20171652. Print 2018 Oct 31.

本文引用的文献

1
Cancer statistics, 2014.癌症统计数据,2014 年。
CA Cancer J Clin. 2014 Jan-Feb;64(1):9-29. doi: 10.3322/caac.21208. Epub 2014 Jan 7.
2
Role of the functional MKK4 promoter variant (-1304T>G) in a decreased risk of prostate cancer: case-control study and meta-analysis.功能性 MKK4 启动子变异体(-1304T>G)在降低前列腺癌风险中的作用:病例对照研究和荟萃分析。
J Cancer Res Clin Oncol. 2012 Sep;138(9):1531-9. doi: 10.1007/s00432-012-1226-y. Epub 2012 Apr 24.
3
Racial disparities in the association between variants on 8q24 and prostate cancer: a systematic review and meta-analysis.
种族差异与 8q24 变异体和前列腺癌之间的关联:系统评价和荟萃分析。
Oncologist. 2012;17(3):312-20. doi: 10.1634/theoncologist.2011-0315. Epub 2012 Mar 1.
4
Individual and cumulative association of prostate cancer susceptibility variants with clinicopathologic characteristics of the disease.个体和累积的前列腺癌易感性变异与疾病的临床病理特征的关联。
Clin Chim Acta. 2010 Sep 6;411(17-18):1232-7. doi: 10.1016/j.cca.2010.04.028. Epub 2010 May 9.
5
Pro variant of TP53 Arg72Pro contributes to esophageal squamous cell carcinoma risk: evidence from a meta-analysis.TP53 Arg72Pro 基因 Pro 变异与食管癌风险相关:来自荟萃分析的证据。
Eur J Cancer Prev. 2010 Jul;19(4):299-307. doi: 10.1097/CEJ.0b013e32833964bc.
6
The rs1447295 and DG8S737 markers on chromosome 8q24 and cancer risk in the Polish population.8q24 染色体上的 rs1447295 和 DG8S737 标记与波兰人群的癌症风险。
Eur J Cancer Prev. 2010 Mar;19(2):167-71. doi: 10.1097/CEJ.0b013e32832945c3.
7
Association of reported prostate cancer risk alleles with PSA levels among men without a diagnosis of prostate cancer.未诊断为前列腺癌的男性中报告的前列腺癌风险等位基因与前列腺特异性抗原水平的关联。
Prostate. 2009 Mar 1;69(4):419-27. doi: 10.1002/pros.20908.
8
Association of genetic polymorphisms at 8q24 with the risk of prostate cancer in a Japanese population.日本人群中8q24基因多态性与前列腺癌风险的关联
Prostate. 2008 Nov 1;68(15):1689-95. doi: 10.1002/pros.20831.
9
8q24 and prostate cancer: association with advanced disease and meta-analysis.8号染色体长臂24区与前列腺癌:与晚期疾病的关联及荟萃分析
Eur J Hum Genet. 2008 Apr;16(4):496-505. doi: 10.1038/sj.ejhg.5201959. Epub 2008 Jan 30.
10
Cumulative association of five genetic variants with prostate cancer.五种基因变异与前列腺癌的累积关联。
N Engl J Med. 2008 Feb 28;358(9):910-9. doi: 10.1056/NEJMoa075819. Epub 2008 Jan 16.