• 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

CHEK2*1100delC 与乳腺癌的关联:系统评价和荟萃分析。

Association Between CHEK2*1100delC and Breast Cancer: A Systematic Review and Meta-Analysis.

机构信息

Department of Epidemiology and Health Statistics, School of Public Health, Anhui Medical University, No. 81 Meishan Road, Hefei, 230032, Anhui, China.

The First Affiliated Hospital of Anhui Medical University, No. 218 Jixi Road, Hefei, 230022, China.

出版信息

Mol Diagn Ther. 2018 Aug;22(4):397-407. doi: 10.1007/s40291-018-0344-x.

DOI:10.1007/s40291-018-0344-x
PMID:29909568
Abstract

INTRODUCTION

The association between the checkpoint kinase 21100delC (CHEK21100delC) and breast cancer has been extensively explored.

OBJECTIVE

In light of the recent publication of studies on these specific findings, particularly regarding male patients with breast cancer, we performed an updated meta-analysis to investigate a more reliable estimate.

METHODS

This meta-analysis included 26 published studies selected in a search of electronic databases up to January 2018, including 118,735 breast cancer cases and 195,807 controls. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the association between 1100delC and breast cancer.

RESULTS

Meta-analysis results suggested that 1100delC contributed to an increased breast cancer risk in overall populations (OR 2.89; 95% CI 2.63-3.16). Subgroup analysis found ORs of 3.13 (95% CI 1.94-5.07) for male breast cancer, 2.88 (95% CI 2.63-3.16) for female breast cancer, 2.87 (95% CI 1.85-4.47) for early-onset breast cancer, 2.92 (95% CI 2.65-3.22) for invasive breast cancer, and 3.21 (95% CI 2.41-4.29) for familial breast cancer. The sensitivity analysis suggested that results of this meta-analysis were generally robust.

CONCLUSION

CHEK2*1100delC is associated with an increased risk of both female and male breast cancer.

摘要

简介

细胞检查点激酶 21100delC(CHEK21100delC)与乳腺癌之间的关联已被广泛研究。

目的

鉴于最近发表了关于这些特定发现的研究,特别是关于男性乳腺癌患者的研究,我们进行了更新的荟萃分析,以调查更可靠的估计。

方法

本荟萃分析纳入了截至 2018 年 1 月在电子数据库中检索到的 26 项已发表的研究,包括 118735 例乳腺癌病例和 195807 例对照。使用比值比(ORs)和 95%置信区间(CIs)来评估 1100delC 与乳腺癌之间的关联。

结果

荟萃分析结果表明,1100delC 导致总体人群乳腺癌风险增加(OR 2.89;95%CI 2.63-3.16)。亚组分析发现,男性乳腺癌的 OR 为 3.13(95%CI 1.94-5.07),女性乳腺癌为 2.88(95%CI 2.63-3.16),早发性乳腺癌为 2.87(95%CI 1.85-4.47),浸润性乳腺癌为 2.92(95%CI 2.65-3.22),家族性乳腺癌为 3.21(95%CI 2.41-4.29)。敏感性分析表明,本荟萃分析的结果总体上是稳健的。

结论

CHEK2*1100delC 与女性和男性乳腺癌的风险增加有关。

相似文献

1
Association Between CHEK2*1100delC and Breast Cancer: A Systematic Review and Meta-Analysis.CHEK2*1100delC 与乳腺癌的关联:系统评价和荟萃分析。
Mol Diagn Ther. 2018 Aug;22(4):397-407. doi: 10.1007/s40291-018-0344-x.
2
CHEK2 1100delC variant and breast cancer risk in Caucasians: a meta-analysis based on 25 studies with 29,154 cases and 37,064 controls.CHEK2基因1100delC变异与高加索人群乳腺癌风险:基于25项研究(共29154例病例和37064例对照)的荟萃分析
Asian Pac J Cancer Prev. 2012;13(7):3501-5. doi: 10.7314/apjcp.2012.13.7.3501.
3
Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers.CHEK2*1100delC携带者的年龄和肿瘤亚型特异性乳腺癌风险估计
J Clin Oncol. 2016 Aug 10;34(23):2750-60. doi: 10.1200/JCO.2016.66.5844. Epub 2016 Jun 6.
4
Increased Risk for Other Cancers in Addition to Breast Cancer for CHEK2*1100delC Heterozygotes Estimated From the Copenhagen General Population Study.从哥本哈根普通人群研究估计,CHEK2*1100delC 杂合子除乳腺癌外其他癌症的风险增加。
J Clin Oncol. 2016 Apr 10;34(11):1208-16. doi: 10.1200/JCO.2015.63.3594. Epub 2016 Feb 16.
5
A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients.寻找 CHEK2:c.1100delC 乳腺癌患者中可改变的遗传因素。
Sci Rep. 2021 Jul 20;11(1):14763. doi: 10.1038/s41598-021-93926-x.
6
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.CHEK2*1100delC相关乳腺癌风险的基因修饰因子。
Genet Med. 2017 May;19(5):599-603. doi: 10.1038/gim.2016.147. Epub 2016 Oct 6.
7
CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls.用于乳腺癌风险临床评估的CHEK2*1100delC基因分型:对26000例患者病例和27000例对照的荟萃分析
J Clin Oncol. 2008 Feb 1;26(4):542-8. doi: 10.1200/JCO.2007.12.5922. Epub 2008 Jan 2.
8
CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.CHEK2基因1100位密码子C缺失与乳腺癌易感性:一项涉及来自10项研究的10860例乳腺癌病例和9065例对照的协作分析。
Am J Hum Genet. 2004 Jun;74(6):1175-82. doi: 10.1086/421251. Epub 2004 Apr 30.
9
Meta-analysis of CHEK2 1100delC variant and colorectal cancer susceptibility.CHEK2 1100delC 变异与结直肠癌易感性的荟萃分析。
Eur J Cancer. 2011 Nov;47(17):2546-51. doi: 10.1016/j.ejca.2011.03.025. Epub 2011 Jul 30.
10
CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population.CHEK2 c.1100delC 突变与芬兰患者群体中男性乳腺癌风险增加相关。
BMC Cancer. 2017 Sep 5;17(1):620. doi: 10.1186/s12885-017-3631-8.

引用本文的文献

1
Short Report: The Variants in in Metastatic Uveal Melanoma.简短报告:转移性葡萄膜黑色素瘤中的变异
J Clin Med. 2025 Apr 18;14(8):2815. doi: 10.3390/jcm14082815.
2
Cohort profile: a nationwide study in Dutch c.1100delC families using the infrastructure of the HEreditary Breast and Ovarian cancer study Netherlands - Hebon-CHEK2.队列特征描述:荷兰使用遗传性乳腺癌和卵巢癌研究荷兰- Hebon-CHEK2 基础设施的 1100delC 家族的全国性研究。
BMJ Open. 2024 Oct 9;14(10):e086688. doi: 10.1136/bmjopen-2024-086688.
3
Breast cancer prediction using different machine learning methods applying multi factors.

本文引用的文献

1
CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population.CHEK2 c.1100delC 突变与芬兰患者群体中男性乳腺癌风险增加相关。
BMC Cancer. 2017 Sep 5;17(1):620. doi: 10.1186/s12885-017-3631-8.
2
Cancer Statistics, 2017.《2017 年癌症统计》
CA Cancer J Clin. 2017 Jan;67(1):7-30. doi: 10.3322/caac.21387. Epub 2017 Jan 5.
3
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.多基因检测队列中的男性乳腺癌:见解与意外结果
应用多因素的不同机器学习方法进行乳腺癌预测。
J Cancer Res Clin Oncol. 2023 Dec;149(19):17133-17146. doi: 10.1007/s00432-023-05388-5. Epub 2023 Sep 29.
4
Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).携带 CHEK2 种系致病性/可能致病性变异个体的管理:美国医学遗传学与基因组学学院(ACMG)的临床实践资源。
Genet Med. 2023 Oct;25(10):100870. doi: 10.1016/j.gim.2023.100870. Epub 2023 Jul 25.
5
Identification of PIMREG as a novel prognostic signature in breast cancer via integrated bioinformatics analysis and experimental validation.通过综合生物信息学分析和实验验证鉴定 PIMREG 作为乳腺癌的一个新的预后标志物。
PeerJ. 2023 Jul 17;11:e15703. doi: 10.7717/peerj.15703. eCollection 2023.
6
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.ENIGMA-CHEK2gether 项目:一项全面研究确定了与乳腺癌风险增加相关的功能失调的 CHEK2 种系错义变异。
Clin Cancer Res. 2023 Aug 15;29(16):3037-3050. doi: 10.1158/1078-0432.CCR-23-0212.
7
Risk of developing a second primary cancer in male breast cancer survivors: a systematic review and meta-analysis.男性乳腺癌幸存者中第二原发性癌症的发病风险:系统评价和荟萃分析。
Br J Cancer. 2022 Nov;127(9):1660-1669. doi: 10.1038/s41416-022-01940-1. Epub 2022 Sep 17.
8
An Update on the General Features of Breast Cancer in Male Patients-A Literature Review.男性乳腺癌一般特征的最新进展——文献综述
Diagnostics (Basel). 2022 Jun 26;12(7):1554. doi: 10.3390/diagnostics12071554.
9
Analysis of the Clinical Advancements for -Related Malignancies Highlights the Lack of Treatment Evidence for -Positive Male Breast Cancer.对 - 相关恶性肿瘤临床进展的分析凸显了 - 阳性男性乳腺癌治疗证据的匮乏。 (注:原文中存在两个未明确的“-”,可能会影响完整准确理解,需根据实际完整内容进一步完善。)
Cancers (Basel). 2022 Jun 28;14(13):3175. doi: 10.3390/cancers14133175.
10
Postmastectomy Reconstruction in Male Breast Cancer.男性乳腺癌乳房切除术后重建。
Breast J. 2022 Mar 29;2022:5482261. doi: 10.1155/2022/5482261. eCollection 2022.
Breast Cancer Res Treat. 2017 Feb;161(3):575-586. doi: 10.1007/s10549-016-4085-4. Epub 2016 Dec 22.
4
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.CHEK2*1100delC相关乳腺癌风险的基因修饰因子。
Genet Med. 2017 May;19(5):599-603. doi: 10.1038/gim.2016.147. Epub 2016 Oct 6.
5
Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.转移性前列腺癌男性患者的遗传性DNA修复基因突变
N Engl J Med. 2016 Aug 4;375(5):443-53. doi: 10.1056/NEJMoa1603144. Epub 2016 Jul 6.
6
Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers.CHEK2*1100delC携带者的年龄和肿瘤亚型特异性乳腺癌风险估计
J Clin Oncol. 2016 Aug 10;34(23):2750-60. doi: 10.1200/JCO.2016.66.5844. Epub 2016 Jun 6.
7
Increased Risk for Other Cancers in Addition to Breast Cancer for CHEK2*1100delC Heterozygotes Estimated From the Copenhagen General Population Study.从哥本哈根普通人群研究估计,CHEK2*1100delC 杂合子除乳腺癌外其他癌症的风险增加。
J Clin Oncol. 2016 Apr 10;34(11):1208-16. doi: 10.1200/JCO.2015.63.3594. Epub 2016 Feb 16.
8
The cancer genetics and pathology of male breast cancer.男性乳腺癌的癌症遗传学与病理学
Histopathology. 2016 Jan;68(1):110-8. doi: 10.1111/his.12862.
9
Rapid Detection Method for the Four Most Common CHEK2 Mutations Based on Melting Profile Analysis.基于熔解曲线分析的四种最常见CHEK2突变快速检测方法
Mol Diagn Ther. 2015 Dec;19(6):419-25. doi: 10.1007/s40291-015-0171-2.
10
Meta-analysis in clinical trials revisited.再谈临床试验中的荟萃分析。
Contemp Clin Trials. 2015 Nov;45(Pt A):139-45. doi: 10.1016/j.cct.2015.09.002. Epub 2015 Sep 4.