Suppr超能文献

血管内皮生长因子A(VEGF-A)基因3'非翻译区的微小RNA结合位点多态性根据种族改变结直肠癌风险:一项荟萃分析。

A microRNA binding site polymorphism in the 3' UTR region of VEGF-A gene modifies colorectal cancer risk based on ethnicity: a meta-analysis.

作者信息

Kontham Sai Sushmitha, Walter Charles Emmanuel Jebaraj, Shankaran Zioni Sangeetha, Ramanathan Arvind, Karuppasamy Nirmala, Johnson Thanka

机构信息

Department of Biotechnology, Sri Ramachandra Institute of Higher Education & Research (formerly Sri Ramachandra Medical College & Research Institute), Chennai, India.

School of Allied Health Sciences, Sree Balaji Medical College and Hospital, Chennai, India.

出版信息

J Egypt Natl Canc Inst. 2022 Apr 25;34(1):18. doi: 10.1186/s43046-022-00118-3.

Abstract

BACKGROUND

Vascular endothelial growth factor A (VEGF-A) plays an integral role in angiogenesis by contributing to growth, development, and metastasis of solid tumors. Recently, a single-nucleotide polymorphism +936C/T located in the VEGF-A 3' untranslated region (UTR) facilitated the susceptibility of colorectal cancer. The association between VEGF-A gene polymorphism +936C/T and colorectal cancer risk has been widely studied in the last decade, but presently, the results furnished remain enigmatic. Hence, the study aimed to investigate the association between VEGF-A +936C/T miRNA binding site polymorphism and the risk of developing colorectal cancer.

METHODS

This meta-analysis included 13 published case-control studies covering 3465 cases (colorectal cancer) and 3476 healthy controls. Publication bias was examined by means of Begg's funnel plots and Egger's regression tests. The quality of the studies included was evaluated using Newcastle-Ottawa scale. Subgroup analyses were performed in accordance to the various ethnicities of the study subjects and the study quality.

RESULTS

From the data obtained, it is implied that VEGF-A +936C/T polymorphism did not correlate with elevated colorectal cancer risk in all genetic models. But the results acquired from the subgroup analysis in over dominant model (CT vs. CC + TT: OR = 1.5047, 95% CI = 1.19-1.90) suggest that VEGF-A +936C/T polymorphism leads to the raise in the risk of developing CRC among the East Asian population. No association was observed in Caucasian and South Asian population.

CONCLUSIONS

Our results indicate that VEGF-A +936C/T polymorphism is not a risk factor for developing CRC in Caucasian and South Asian population. However, the East Asian population was related to an increased risk of developing colorectal cancer due to the presence of the minor allele.

摘要

背景

血管内皮生长因子A(VEGF-A)通过促进实体瘤的生长、发展和转移,在血管生成中发挥着不可或缺的作用。最近,位于VEGF-A 3'非翻译区(UTR)的单核苷酸多态性+936C/T增加了结直肠癌的易感性。在过去十年中,VEGF-A基因多态性+936C/T与结直肠癌风险之间的关联已得到广泛研究,但目前所提供的结果仍不明确。因此,本研究旨在探讨VEGF-A +936C/T miRNA结合位点多态性与结直肠癌发生风险之间的关联。

方法

本荟萃分析纳入了13项已发表的病例对照研究,涵盖3465例病例(结直肠癌)和3476例健康对照。采用Begg漏斗图和Egger回归检验来检验发表偏倚。使用纽卡斯尔-渥太华量表评估纳入研究的质量。根据研究对象的不同种族和研究质量进行亚组分析。

结果

从获得的数据来看,在所有遗传模型中,VEGF-A +936C/T多态性与结直肠癌风险升高无关。但在超显性模型的亚组分析中获得的结果(CT与CC + TT相比:OR = 1.5047,95%CI = 1.19 - 1.90)表明,VEGF-A +936C/T多态性会导致东亚人群患结直肠癌的风险增加。在白种人和南亚人群中未观察到关联。

结论

我们的结果表明,VEGF-A +936C/T多态性不是白种人和南亚人群患结直肠癌的危险因素。然而,由于存在次要等位基因,东亚人群患结直肠癌的风险增加。

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