Association of VEGF-2549I/D promoter polymorphism with gastrointestinal tract cancer risk: a meta-analysis

IF 1.2 Q4 GENETICS & HEREDITY
Deepanshi Mahajan, Vasudha Sambyal, Kamlesh Guleria
{"title":"Association of VEGF-2549I/D promoter polymorphism with gastrointestinal tract cancer risk: a meta-analysis","authors":"Deepanshi Mahajan, Vasudha Sambyal, Kamlesh Guleria","doi":"10.1186/s43042-024-00535-0","DOIUrl":null,"url":null,"abstract":"Gastrointestinal tract (GIT) cancers are complex disorders affecting millions of people worldwide. The vascular endothelial growth factor (VEGF) helps in the development of different GIT cancers by promoting abnormal angiogenesis in cancer cells. The role of VEGF-2549I/D polymorphism in influencing GIT cancer susceptibility has been studied in different populations with inconclusive results. Therefore, the relationship between VEGF-2549I/D polymorphism with GIT susceptibility was studied by performing a meta-analysis study. Various online databases were used for identifying the articles. Based on study selection criteria, five studies on different GIT cancers including 1178 patients and 1520 controls were included in the meta-analysis. The accuracy of the study results was determined by performing a trial sequential analysis. In this study, the VEGF-2549I/D polymorphism did not influence the GIT cancer susceptibility in the overall analysis as well as when stratified according to ethnicity (p > 0.05). Stratification of all the studies based on the different GIT cancers reported an increased susceptibility to gastric cancer under different genetic models including allele contrast (OR = 1.67, CI = 1.294–2.157, p = 0.00008), recessive (OR = 1.68, CI = 1.056–2.660, p = 0.029), dominant (OR = 2.49, CI = 1.617–3.823, p = 0.00003), over-dominant (OR = 1.52, CI = 1.055–2.177, p = 0.025), II vs DD (OR = 2.97, CI = 1.692–5.208, p = 0.00015) and ID vs DD model (OR = 2.35, CI = 1.501–3.669, p = 0.00018). There was no relationship between VEGF-2549I/D promoter polymorphism and GIT cancer susceptibility in the overall population and also in different ethnic groups. Stratification analysis revealed higher susceptibility towards gastric cancer development with VEGF-2549I/D polymorphism.","PeriodicalId":39112,"journal":{"name":"Egyptian Journal of Medical Human Genetics","volume":null,"pages":null},"PeriodicalIF":1.2000,"publicationDate":"2024-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Egyptian Journal of Medical Human Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s43042-024-00535-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Gastrointestinal tract (GIT) cancers are complex disorders affecting millions of people worldwide. The vascular endothelial growth factor (VEGF) helps in the development of different GIT cancers by promoting abnormal angiogenesis in cancer cells. The role of VEGF-2549I/D polymorphism in influencing GIT cancer susceptibility has been studied in different populations with inconclusive results. Therefore, the relationship between VEGF-2549I/D polymorphism with GIT susceptibility was studied by performing a meta-analysis study. Various online databases were used for identifying the articles. Based on study selection criteria, five studies on different GIT cancers including 1178 patients and 1520 controls were included in the meta-analysis. The accuracy of the study results was determined by performing a trial sequential analysis. In this study, the VEGF-2549I/D polymorphism did not influence the GIT cancer susceptibility in the overall analysis as well as when stratified according to ethnicity (p > 0.05). Stratification of all the studies based on the different GIT cancers reported an increased susceptibility to gastric cancer under different genetic models including allele contrast (OR = 1.67, CI = 1.294–2.157, p = 0.00008), recessive (OR = 1.68, CI = 1.056–2.660, p = 0.029), dominant (OR = 2.49, CI = 1.617–3.823, p = 0.00003), over-dominant (OR = 1.52, CI = 1.055–2.177, p = 0.025), II vs DD (OR = 2.97, CI = 1.692–5.208, p = 0.00015) and ID vs DD model (OR = 2.35, CI = 1.501–3.669, p = 0.00018). There was no relationship between VEGF-2549I/D promoter polymorphism and GIT cancer susceptibility in the overall population and also in different ethnic groups. Stratification analysis revealed higher susceptibility towards gastric cancer development with VEGF-2549I/D polymorphism.
VEGF-2549I/D 启动子多态性与胃肠道癌症风险的关系:荟萃分析
胃肠道癌症是一种复杂的疾病,影响着全球数百万人。血管内皮生长因子(VEGF)通过促进癌细胞的异常血管生成,有助于不同胃肠道癌症的发展。关于 VEGF-2549I/D 多态性在影响 GIT 癌症易感性方面的作用,已在不同人群中进行了研究,但结果尚无定论。因此,我们通过荟萃分析研究了 VEGF-2549I/D 多态性与 GIT 易感性之间的关系。研究人员使用了各种在线数据库来查找文章。根据研究选择标准,荟萃分析纳入了五项关于不同 GIT 癌症的研究,包括 1178 例患者和 1520 例对照。研究结果的准确性通过进行试验序列分析来确定。在这项研究中,VEGF-2549I/D 多态性在总体分析中以及根据种族进行分层时都不会影响 GIT 癌的易感性(P > 0.05)。根据不同的 GIT 癌症对所有研究进行分层后发现,在不同的遗传模式下胃癌易感性增加,包括等位基因对比(OR = 1.67,CI = 1.294-2.157,p = 0.00008)、隐性(OR = 1.68,CI = 1.056-2.660,p = 0.029)、显性(OR = 2.49,CI = 1.617-3.823,p = 0.00003)、过显性(OR = 1.52,CI = 1.055-2.177,p = 0.025)、II vs DD(OR = 2.97,CI = 1.692-5.208,p = 0.00015)和 ID vs DD 模型(OR = 2.35,CI = 1.501-3.669,p = 0.00018)。在总体人群和不同种族群体中,VEGF-2549I/D 启动子多态性与 GIT 癌易感性之间没有关系。分层分析表明,VEGF-2549I/D 多态性对胃癌的易感性更高。
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 求助全文
来源期刊
Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics Medicine-Genetics (clinical)
CiteScore
2.20
自引率
7.70%
发文量
150
审稿时长
18 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信