Receptors of advanced glycation end products in oral squamous cell carcinoma: A systematic review

Tumor discovery Pub Date : 2020-08-23 DOI:10.36922/td.244
Sinduja Palati, P. Ramani, H. Sherlin, S. Gheena, A. Ramasubramanian, K. Don, G. Jayaraj, Archana Santhanam
{"title":"Receptors of advanced glycation end products in oral squamous cell carcinoma: A systematic review","authors":"Sinduja Palati, P. Ramani, H. Sherlin, S. Gheena, A. Ramasubramanian, K. Don, G. Jayaraj, Archana Santhanam","doi":"10.36922/td.244","DOIUrl":null,"url":null,"abstract":"Oxidative stress markers have been shown to be elevated in oral squamous cell carcinomas; plays a crucial role in the build-up of advanced glycation end-receptors of advanced glycation end (AGE-RAGE) products; and has been shown to exacerbate cellular dysfunction, vascular change, apoptosis, and activate inflammatory pathways. The purpose of this study is to assess comprehensively the involvement of RAGE in oral squamous cell malignancies. The findings imply that these receptors and their associated ligands play a significant role in the growth and spread of the tumor, hence impacting the prognosis and life expectancy of the affected individual. This comprehensive review uncovers promising evidence for the clinical use of these molecules, such as RAGEs, in prognostic considerations or as molecular targets for therapy. The available literature shows a role for RAGE in invasion, migration, and angiogenesis in oral cancers. These preliminary findings are encouraging for the therapeutic use of these molecules for prognostic considerations or molecularly targeted therapy.","PeriodicalId":94260,"journal":{"name":"Tumor discovery","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tumor discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36922/td.244","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Oxidative stress markers have been shown to be elevated in oral squamous cell carcinomas; plays a crucial role in the build-up of advanced glycation end-receptors of advanced glycation end (AGE-RAGE) products; and has been shown to exacerbate cellular dysfunction, vascular change, apoptosis, and activate inflammatory pathways. The purpose of this study is to assess comprehensively the involvement of RAGE in oral squamous cell malignancies. The findings imply that these receptors and their associated ligands play a significant role in the growth and spread of the tumor, hence impacting the prognosis and life expectancy of the affected individual. This comprehensive review uncovers promising evidence for the clinical use of these molecules, such as RAGEs, in prognostic considerations or as molecular targets for therapy. The available literature shows a role for RAGE in invasion, migration, and angiogenesis in oral cancers. These preliminary findings are encouraging for the therapeutic use of these molecules for prognostic considerations or molecularly targeted therapy.
口腔鳞状细胞癌晚期糖基化终产物受体:系统综述
氧化应激标志物已被证明在口腔鳞状细胞癌中升高;在晚期糖基化末端(AGE-RAGE)产物的晚期糖基化末端受体的构建中起着至关重要的作用;并已被证明会加剧细胞功能障碍、血管改变、细胞凋亡和激活炎症途径。本研究的目的是全面评估RAGE在口腔鳞状细胞恶性肿瘤中的作用。研究结果表明,这些受体及其相关配体在肿瘤的生长和扩散中起着重要作用,从而影响患者的预后和预期寿命。这项全面的综述揭示了这些分子(如RAGEs)在预后考虑或作为治疗分子靶点方面的临床应用的有希望的证据。现有文献显示RAGE在口腔癌的侵袭、迁移和血管生成中起作用。这些初步发现对于这些分子用于预后考虑或分子靶向治疗的治疗用途是令人鼓舞的。
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