Microrna-1/206 Target both Monocarboxylate Transporter(MCT)-4 and Vascular Endothelial Growth Factor(VEGF)Genes Leading to Inhibition of Tumor Growth

Anas Khaleel, A. Elbakkoush, Amneh H. Tarkhan, Aiman Mahdi
{"title":"Microrna-1/206 Target both Monocarboxylate Transporter(MCT)-4 and Vascular Endothelial Growth Factor(VEGF)Genes Leading to Inhibition of Tumor Growth","authors":"Anas Khaleel, A. Elbakkoush, Amneh H. Tarkhan, Aiman Mahdi","doi":"10.1145/3309129.3309144","DOIUrl":null,"url":null,"abstract":"Colorectal cancer is one of the most common types of cancer in the world, and its incidence is mostly influenced by lifestyle factors. Despite having a much smaller role, genetics also affects the susceptibility and development of colorectal cancer. The aim of the present study is to investigate the regulatory functions of candidate microRNAs (miRs) 1 and 206 in the context of solute carrier family 16 member 3 (SLC16A3) and vascular endothelial growth factor (VEGF) expression. To achieve this, 24 oncogenes targeted by miR-1 and miR-206 were analyzed via GeneMANIA. The miRTarBase database was then employed to ascertain the nature of the miR-oncogene relationship. Our findings illustrate that miR-1/206 indirectly reduce CRC growth and infiltration by targeting the both the SLC16A3 and VEGF genes. Moreover, miR-1/206 targets the VEGF gene to reduce tumor angiogenesis and vasculature. Conclusively, the results of the current study illustrate a novel regulation pathway in CRC cells, suggesting new potential lines of CRC therapy.","PeriodicalId":326530,"journal":{"name":"Proceedings of the 5th International Conference on Bioinformatics Research and Applications","volume":"42 4 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the 5th International Conference on Bioinformatics Research and Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1145/3309129.3309144","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Colorectal cancer is one of the most common types of cancer in the world, and its incidence is mostly influenced by lifestyle factors. Despite having a much smaller role, genetics also affects the susceptibility and development of colorectal cancer. The aim of the present study is to investigate the regulatory functions of candidate microRNAs (miRs) 1 and 206 in the context of solute carrier family 16 member 3 (SLC16A3) and vascular endothelial growth factor (VEGF) expression. To achieve this, 24 oncogenes targeted by miR-1 and miR-206 were analyzed via GeneMANIA. The miRTarBase database was then employed to ascertain the nature of the miR-oncogene relationship. Our findings illustrate that miR-1/206 indirectly reduce CRC growth and infiltration by targeting the both the SLC16A3 and VEGF genes. Moreover, miR-1/206 targets the VEGF gene to reduce tumor angiogenesis and vasculature. Conclusively, the results of the current study illustrate a novel regulation pathway in CRC cells, suggesting new potential lines of CRC therapy.
Microrna-1/206同时靶向单羧酸转运蛋白(MCT)-4和血管内皮生长因子(VEGF)基因,从而抑制肿瘤生长
结直肠癌是世界上最常见的癌症之一,其发病率主要受生活方式因素的影响。尽管基因的作用要小得多,但它也会影响结直肠癌的易感性和发展。本研究的目的是研究候选microRNAs (miRs) 1和206在溶质载体家族16成员3 (SLC16A3)和血管内皮生长因子(VEGF)表达中的调节功能。为了实现这一点,通过GeneMANIA分析了miR-1和miR-206靶向的24个癌基因。然后使用miRTarBase数据库来确定mir -癌基因关系的性质。我们的研究结果表明,miR-1/206通过靶向SLC16A3和VEGF基因间接降低CRC的生长和浸润。此外,miR-1/206靶向VEGF基因减少肿瘤血管生成和血管。总之,本研究的结果阐明了CRC细胞中的一种新的调控途径,为CRC治疗提供了新的潜在途径。
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
自引率
0.00%
发文量
0
×
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