• 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

多态性 rs1051740 与卵巢癌风险的关联:一项荟萃分析。

Association between polymorphism rs1051740 and the risk of ovarian cancer: a meta-analysis.

机构信息

a Department of Obstetrics and Gynecology, Beijing Friendship Hospital, Capital Medical University , Beijing , China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):2338-2342. doi: 10.1080/21691401.2019.1622551.

DOI:10.1080/21691401.2019.1622551
PMID:31174441
Abstract

We carried out a meta-analysis of case-control studies to determine whether epoxide hydrolase 1 () gene polymorphism rs1051740 was related to the risk of ovarian cancer. Electronic databases were searched for relevant articles published in English or Chinese language. We calculated crude odds ratios (ORs) with their 95% confidence intervals (95% CIs) to assess the relationship of polymorphism rs1051740 with ovarian cancer risk. In addition, subgroup analyses were also conducted based on ethnicity and control source. Between-study heterogeneity was inspected with test and statistic. Five eligible studies with a total of 1919 ovarian cancer patients and 1829 controls were ultimately included in the present meta-analysis. Overall results demonstrated that the association between polymorphism rs1051740 and ovarian cancer risk had no statistical significance either in total analysis or in subgroup analyses by ethnicity and source of control. polymorphism rs1051740 may have no independent effect on ovarian cancer susceptibility.

摘要

我们进行了一项病例对照研究的荟萃分析,以确定环氧化物水解酶 1()基因多态性 rs1051740 是否与卵巢癌的风险相关。检索了英文和中文文献的电子数据库,以获取相关文章。我们计算了粗比值比(OR)及其 95%置信区间(95%CI),以评估 多态性 rs1051740 与卵巢癌风险的关系。此外,还根据种族和对照来源进行了亚组分析。用 检验和 统计检验来检测组间异质性。最终纳入了五项符合条件的研究,共包括 1919 名卵巢癌患者和 1829 名对照。总体结果表明,在总分析或按种族和对照来源进行的亚组分析中,多态性 rs1051740 与卵巢癌风险之间均无统计学意义。多态性 rs1051740 可能对卵巢癌易感性没有独立影响。

相似文献

1
Association between polymorphism rs1051740 and the risk of ovarian cancer: a meta-analysis.多态性 rs1051740 与卵巢癌风险的关联:一项荟萃分析。
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):2338-2342. doi: 10.1080/21691401.2019.1622551.
2
Systematic review and meta-analysis of the relationship between EPHX1 polymorphisms and colorectal cancer risk.EPHX1 多态性与结直肠癌风险关系的系统评价和荟萃分析。
PLoS One. 2012;7(8):e43821. doi: 10.1371/journal.pone.0043821. Epub 2012 Aug 23.
3
Oxidative stress-related genes ( and polymorphism and risk of pre-eclampsia: a meta-analysis.氧化应激相关基因(与子痫前期的多态性及风险:一项荟萃分析)
J Matern Fetal Neonatal Med. 2022 Dec;35(25):5526-5538. doi: 10.1080/14767058.2021.1887123. Epub 2021 Feb 15.
4
Association between EPHX1 rs1051740 and lung cancer susceptibility: a meta-analysis.EPHX1基因rs1051740与肺癌易感性的关联:一项荟萃分析。
Int J Clin Exp Med. 2015 Oct 15;8(10):17941-9. eCollection 2015.
5
EPHX1 rs1051740 T>C (Tyr113His) is strongly associated with acute myeloid leukemia and KMT2A rearrangements in early age.EPHX1 rs1051740 T>C(Tyr113His)与急性髓细胞白血病和 KMT2A 重排密切相关,且在早年发病。
Arch Toxicol. 2018 Jun;92(6):2001-2012. doi: 10.1007/s00204-018-2198-8. Epub 2018 Mar 31.
6
Association between microsomal epoxide hydrolase 1 polymorphisms and susceptibility to esophageal cancer: a meta-analysis.微粒体环氧化物水解酶1基因多态性与食管癌易感性的关联:一项荟萃分析。
Tumour Biol. 2013 Aug;34(4):2383-8. doi: 10.1007/s13277-013-0787-y. Epub 2013 May 17.
7
Lack of association between EPHX1 polymorphism and esophageal cancer risk: evidence from meta-analysis.EPHX1基因多态性与食管癌风险之间无关联:荟萃分析证据
Dis Esophagus. 2015 Feb-Mar;28(2):164-71. doi: 10.1111/dote.12169. Epub 2014 Feb 20.
8
Association between microsomal epoxide hydrolase 1 T113C polymorphism and susceptibility to lung cancer.微粒体环氧化物水解酶1 T113C多态性与肺癌易感性之间的关联。
Tumour Biol. 2013 Apr;34(2):1045-52. doi: 10.1007/s13277-012-0644-4. Epub 2013 Feb 3.
9
Systematic Review and Meta-Analysis of the Relationship between EPHX1 Polymorphisms and the Risk of Head and Neck Cancer.EPHX1基因多态性与头颈癌风险关系的系统评价和Meta分析
PLoS One. 2015 Apr 29;10(4):e0123347. doi: 10.1371/journal.pone.0123347. eCollection 2015.
10
Association of EPHX1 polymorphisms with plasma concentration of carbamazepine in epileptic patients: Systematic review and meta-analysis.EPHX1 多态性与癫痫患者卡马西平血浆浓度的相关性:系统评价和荟萃分析。
J Clin Neurosci. 2021 Sep;91:159-171. doi: 10.1016/j.jocn.2021.07.009. Epub 2021 Jul 13.

引用本文的文献

1
EPHX1 enhances drug resistance to regorafenib by activating the JAK/STAT signaling pathway in hepatocellular carcinoma cell lines.EPHX1通过激活肝癌细胞系中的JAK/STAT信号通路增强对瑞戈非尼的耐药性。
Hereditas. 2025 Jul 31;162(1):148. doi: 10.1186/s41065-025-00517-1.
2
Association between XRCC3 rs861539 Polymorphism and the Risk of Ovarian Cancer: Meta-Analysis and Trial Sequential Analysis.XRCC3 rs861539 多态性与卵巢癌风险的关联:Meta 分析和试验序贯分析。
Biomed Res Int. 2022 Aug 8;2022:3915402. doi: 10.1155/2022/3915402. eCollection 2022.
3
The association between single nucleotide polymorphisms and ovarian cancer risk: A systematic review and network meta-analysis.
单核苷酸多态性与卵巢癌风险的关联:系统评价和网络荟萃分析。
Cancer Med. 2023 Jan;12(1):541-556. doi: 10.1002/cam4.4891. Epub 2022 May 30.
4
The effect of folate intake on ovarian cancer risk: A meta-analysis of observational studies.叶酸摄入量对卵巢癌风险的影响:观察性研究的荟萃分析。
Medicine (Baltimore). 2021 Jan 22;100(3):e22605. doi: 10.1097/MD.0000000000022605.
5
Clinical outcomes and safety of apatinib monotherapy in the treatment of patients with advanced epithelial ovarian carcinoma who progressed after standard regimens and the analysis of the polymorphism.阿帕替尼单药治疗标准方案治疗后进展的晚期上皮性卵巢癌患者的临床疗效和安全性及多态性分析
Oncol Lett. 2020 Sep;20(3):3035-3045. doi: 10.3892/ol.2020.11857. Epub 2020 Jul 10.