The association between HIC1 methylation and ovarian cancer: a meta-analysis

IF 0.5 4区 医学 Q4 OBSTETRICS & GYNECOLOGY European journal of gynaecological oncology Pub Date : 2022-04-15 DOI:10.31083/j.ejgo4302037
Jiayi Guo, Lifang Sun, Qingqing Lv
{"title":"The association between HIC1 methylation and ovarian cancer: a meta-analysis","authors":"Jiayi Guo, Lifang Sun, Qingqing Lv","doi":"10.31083/j.ejgo4302037","DOIUrl":null,"url":null,"abstract":"Objective : HIC1 is a tumor suppressor gene (TSG) located in the 17p13.3 region that encodes a transcriptional repressor. Research published over the past few years indicates that HIC1 methylation is a critical factor in the oncogenesis of ovarian cancer (OC). However, previous studies had only small sample sizes and thus were unable to reach firm conclusions. Data Sources : Therefore, we performed a meta-analysis to further investigate the association between HIC1 methylation and OC. Studies related to HIC1 methylation and OC were identified from searches of PubMed, EMBASE, Medline and CNKI. Methods of Study Selection : Odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the association between the two factors. Subgroup analysis and Begg’s test were used to evaluate heterogeneity and publication bias. From 591 studies, 7 were selected for meta-analysis and these comprised 455 cases and 278 controls. Tabulation, Integration and Results : A significant association between HIC1 methylation and OC was found under the fixed-effects model (OR = 4.306, 95% CI = 2.846 to 6.515). Subgroup analysis of the control type yielded a less tight association (OR = 4.143, p = 0.147, I 2 = 41.1%). Finally, we conducted analysis of the Cancer Genome Atlas (TCGA) data and found higher HIC1 methylation levels in OC compared to adjacent non-tumor tissue. Conclusion : In conclusion, this meta-analysis found that HIC1 methylation was strongly associated with OC.","PeriodicalId":11903,"journal":{"name":"European journal of gynaecological oncology","volume":" ","pages":""},"PeriodicalIF":0.5000,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of gynaecological oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.31083/j.ejgo4302037","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective : HIC1 is a tumor suppressor gene (TSG) located in the 17p13.3 region that encodes a transcriptional repressor. Research published over the past few years indicates that HIC1 methylation is a critical factor in the oncogenesis of ovarian cancer (OC). However, previous studies had only small sample sizes and thus were unable to reach firm conclusions. Data Sources : Therefore, we performed a meta-analysis to further investigate the association between HIC1 methylation and OC. Studies related to HIC1 methylation and OC were identified from searches of PubMed, EMBASE, Medline and CNKI. Methods of Study Selection : Odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the association between the two factors. Subgroup analysis and Begg’s test were used to evaluate heterogeneity and publication bias. From 591 studies, 7 were selected for meta-analysis and these comprised 455 cases and 278 controls. Tabulation, Integration and Results : A significant association between HIC1 methylation and OC was found under the fixed-effects model (OR = 4.306, 95% CI = 2.846 to 6.515). Subgroup analysis of the control type yielded a less tight association (OR = 4.143, p = 0.147, I 2 = 41.1%). Finally, we conducted analysis of the Cancer Genome Atlas (TCGA) data and found higher HIC1 methylation levels in OC compared to adjacent non-tumor tissue. Conclusion : In conclusion, this meta-analysis found that HIC1 methylation was strongly associated with OC.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
HIC1甲基化与卵巢癌的关系:一项荟萃分析
目的:HIC1是一个位于17p13.3区的肿瘤抑制基因,编码一个转录抑制因子。过去几年发表的研究表明,HIC1甲基化是卵巢癌症(OC)发生的关键因素。然而,以前的研究样本量很小,因此无法得出确切的结论。数据来源:因此,我们进行了一项荟萃分析,以进一步研究HIC1甲基化与OC之间的关系。从PubMed、EMBASE、Medline和CNKI的搜索中确定了与HIC1甲基化和OC相关的研究。研究选择方法:使用比值比(OR)和95%置信区间(CI)来评估这两个因素之间的相关性。亚组分析和Begg检验用于评估异质性和发表偏倚。从591项研究中,选择7项进行荟萃分析,其中包括455例病例和278例对照。制表、积分和结果:在固定效应模型下,HIC1甲基化和OC之间存在显著相关性(OR=4.306,95%CI=2.846至6.515)。对照组的亚组分析显示相关性较低(OR=4.143,p=0.147,I2=41.1%)。最后,我们对癌症基因组图谱(TCGA)数据进行了分析,发现OC中的HIC1甲基化水平高于邻近的非肿瘤组织。结论:总之,本荟萃分析发现HIC1甲基化与OC密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
25.00%
发文量
58
审稿时长
1 months
期刊介绍: EJGO is dedicated to publishing editorial articles in the Distinguished Expert Series and original research papers, case reports, letters to the Editor, book reviews, and newsletters. The Journal was founded in 1980 the second gynaecologic oncology hyperspecialization Journal in the world. Its aim is the diffusion of scientific, clinical and practical progress, and knowledge in female neoplastic diseases in an interdisciplinary approach among gynaecologists, oncologists, radiotherapists, surgeons, chemotherapists, pathologists, epidemiologists, and so on.
期刊最新文献
Timing and duration of bevacizumab treatment and survival in patients with recurrent ovarian, fallopian tube, and peritoneal cancer: a multi-institution study. Vulvar cancer in young woman—case report Identification of an immune-related metabolic gene signature to predict possible prognosis in endometrial cancer and reveals immune landscape feature Evaluation of colposcopy and LEEP results performed in gynecology and gynecological oncology surgery services The infrequent large pelvi-perineal tumors as a surgical dilemma: en bloc resection and long-term results
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1