• 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

E-钙黏蛋白(CDH1)-C160A 多态性与结直肠癌易感性的关系:一项荟萃分析。

The E-cadherin (CDH1) -C160A polymorphism and colorectal cancer susceptibility: a meta-analysis.

机构信息

Department of Oncology, Southwest Hospital, Third Military Medical University, Chongqing, PR China.

出版信息

DNA Cell Biol. 2012 Jun;31(6):1070-7. doi: 10.1089/dna.2011.1380. Epub 2012 Feb 17.

DOI:10.1089/dna.2011.1380
PMID:22339265
Abstract

E-cadherin, encoded by the CDH1 gene, involves in invasion and metastasis of cancer cells. CDH1 -C160A polymorphism was shown to contribute to genetic susceptibility to colorectal cancer (CRC). However, the results from different studies remain controversial. This study was conducted to further explore the association between CDH1 -C160A genetic polymorphism and CRC susceptibility by means of a meta-analysis. A comprehensive literature search was conducted to identify all case-control studies of CDH1 -C160A polymorphism and risk for CRC. A total of nine eligible studies, including 7954 CRC cases and 7369 controls, were identified to the meta-analysis. On the whole, the meta-analysis indicated that CDH1 -C160A genetic polymorphism could reduce the risk of CRC under AA versus CC contrast (odds ratio [OR]=0.86, 95% confidence interval [CI]=0.75-0.98, p(heterogeneity)=0.11), recessive model (OR=0.88, 95% CI=0.77-0.99, p(heterogeneity)=0.23), dominant model (OR=0.92, 95% CI=0.87-0.99, p(heterogeneity)=0.11), and allele A versus allele C contrast (OR=0.93, 95% CI=0.88-0.98, p(heterogeneity)=0.26). A conclusion could be drawn from the research that CDH1 -C160A polymorphism provides a possible protection against CRC, which is especially evident in Caucasian and hospital populations.

摘要

E-钙黏蛋白由 CDH1 基因编码,参与癌细胞的侵袭和转移。CDH1-C160A 多态性被认为与结直肠癌(CRC)的遗传易感性有关。然而,来自不同研究的结果仍然存在争议。本研究通过荟萃分析进一步探讨了 CDH1-C160A 遗传多态性与 CRC 易感性的关系。进行了全面的文献检索,以确定所有关于 CDH1-C160A 多态性与 CRC 风险的病例对照研究。共有 9 项符合条件的研究,包括 7954 例 CRC 病例和 7369 例对照,被纳入荟萃分析。总的来说,荟萃分析表明,CDH1-C160A 遗传多态性在 AA 与 CC 对比(优势比[OR]=0.86,95%置信区间[CI]=0.75-0.98,p(异质性)=0.11)、隐性模型(OR=0.88,95% CI=0.77-0.99,p(异质性)=0.23)、显性模型(OR=0.92,95% CI=0.87-0.99,p(异质性)=0.11)和等位基因 A 与等位基因 C 对比(OR=0.93,95% CI=0.88-0.98,p(异质性)=0.26)中降低 CRC 的风险。从这项研究中可以得出结论,CDH1-C160A 多态性为 CRC 提供了一种可能的保护,这在白人和医院人群中尤为明显。

相似文献

1
The E-cadherin (CDH1) -C160A polymorphism and colorectal cancer susceptibility: a meta-analysis.E-钙黏蛋白(CDH1)-C160A 多态性与结直肠癌易感性的关系:一项荟萃分析。
DNA Cell Biol. 2012 Jun;31(6):1070-7. doi: 10.1089/dna.2011.1380. Epub 2012 Feb 17.
2
Association between the Epithelial Cadherin - 160C/A Polymorphism and Colorectal Cancer Risk: Evidence from a Meta-Analysis.上皮钙黏蛋白-160C/A多态性与结直肠癌风险的关联:一项荟萃分析的证据
Crit Rev Eukaryot Gene Expr. 2017;27(4):347-354. doi: 10.1615/CritRevEukaryotGeneExpr.2017020525.
3
E-cadherin (CDH1) gene -160C/A polymorphism and the risk of colorectal cancer: A meta-analysis involving 17,291 subjects.E-钙黏蛋白(CDH1)基因-160C/A 多态性与结直肠癌风险的关系:一项包含 17291 例个体的荟萃分析。
J Gene Med. 2021 Oct;23(10):e3370. doi: 10.1002/jgm.3370. Epub 2021 Jul 2.
4
E-cadherin (CDH1) gene promoter polymorphism and the risk of colorectal cancer : a meta-analysis.E-钙黏蛋白(CDH1)基因启动子多态性与结直肠癌风险:荟萃分析。
Int J Colorectal Dis. 2012 Feb;27(2):151-8. doi: 10.1007/s00384-011-1320-7. Epub 2011 Oct 14.
5
CDH1 rs9929218 variant at 16q22.1 contributes to colorectal cancer susceptibility.位于16q22.1的CDH1基因rs9929218变异体与结直肠癌易感性相关。
Oncotarget. 2016 Jul 26;7(30):47278-47286. doi: 10.18632/oncotarget.9758.
6
Lack of Association between the CDH1 -160C>A Polymorphism and Risk of Gastrointestinal Cancer - a Meta-Analysis.CDH1基因-160C>A多态性与胃肠道癌风险之间无关联——一项荟萃分析
Asian Pac J Cancer Prev. 2016;17(5):2415-21.
7
Association of clinicopathological features with E-cadherin (CDH1) gene-160 C>A promoter polymorphism in Turkish colorectal cancer patients.土耳其结直肠癌患者临床病理特征与E-钙黏蛋白(CDH1)基因-160 C>A启动子多态性的关联
J Cancer Res Ther. 2019 Jan-Mar;15(1):26-31. doi: 10.4103/jcrt.JCRT_1277_16.
8
The CDH1 -160C/A polymorphism is associated with breast cancer: evidence from a meta-analysis.CDH1基因-160C/A多态性与乳腺癌相关:一项荟萃分析的证据。
World J Surg Oncol. 2016 Jun 27;14(1):169. doi: 10.1186/s12957-016-0927-0.
9
CDH1 -160C>A gene polymorphism is an ethnicity-dependent risk factor for gastric cancer.CDH1-160C>A 基因多态性是一种与种族相关的胃癌风险因素。
Cytokine. 2011 Aug;55(2):266-73. doi: 10.1016/j.cyto.2011.04.008. Epub 2011 May 12.
10
The epithelial cadherin -160C/A polymorphism is associated with decreased risk of colorectal cancer: a case-control study.上皮钙黏蛋白 160C/A 多态性与结直肠癌风险降低相关:一项病例对照研究。
Clin Exp Med. 2020 Feb;20(1):73-78. doi: 10.1007/s10238-019-00586-3. Epub 2019 Oct 17.

引用本文的文献

1
The epithelial cadherin -160C/A polymorphism is associated with decreased risk of colorectal cancer: a case-control study.上皮钙黏蛋白 160C/A 多态性与结直肠癌风险降低相关:一项病例对照研究。
Clin Exp Med. 2020 Feb;20(1):73-78. doi: 10.1007/s10238-019-00586-3. Epub 2019 Oct 17.
2
The CDH1 -160C/A polymorphism is associated with breast cancer: evidence from a meta-analysis.CDH1基因-160C/A多态性与乳腺癌相关:一项荟萃分析的证据。
World J Surg Oncol. 2016 Jun 27;14(1):169. doi: 10.1186/s12957-016-0927-0.
3
Regulatory Variants and Disease: The E-Cadherin -160C/A SNP as an Example.
调控变异与疾病:以E-钙黏蛋白-160C/A单核苷酸多态性为例
Mol Biol Int. 2014;2014:967565. doi: 10.1155/2014/967565. Epub 2014 Sep 2.
4
Contribution of cyclin D1 (CCND1) and E-cadherin (CDH1) alterations to colorectal cancer susceptibility: a case-control study.细胞周期蛋白D1(CCND1)和E-钙黏蛋白(CDH1)改变对结直肠癌易感性的影响:一项病例对照研究。
Tumour Biol. 2014 Dec;35(12):12059-67. doi: 10.1007/s13277-014-2505-9. Epub 2014 Aug 22.
5
Interleukin-1α -899 (+4845) C→T polymorphism is not associated with aggressive periodontitis susceptibility: A meta-analysis based on 19 case-control studies.白细胞介素-1α -899(+4845)C→T多态性与侵袭性牙周炎易感性无关:基于19项病例对照研究的荟萃分析
Biomed Rep. 2014 May;2(3):378-383. doi: 10.3892/br.2014.240. Epub 2014 Feb 19.