TP53 Gene Signaling Pathways and Protein Interactions with MDM2 and HPV in Oral Cancers andndash; A Review

Diaga Sp, D. Djp, D. Yacouba, Abdoul Bas, Mawulolo Gf, T. Silly, M. Babacar, Maguette Sn, F. Oumar, D. Alioune, Rokhaya Nd
{"title":"TP53 Gene Signaling Pathways and Protein Interactions with MDM2 and HPV in Oral Cancers andndash; A Review","authors":"Diaga Sp, D. Djp, D. Yacouba, Abdoul Bas, Mawulolo Gf, T. Silly, M. Babacar, Maguette Sn, F. Oumar, D. Alioune, Rokhaya Nd","doi":"10.37421/1747-0862.2021.15.504","DOIUrl":null,"url":null,"abstract":"Oral cancers are heterogeneous group of tumors in topography (they can be localized at on the lips, tongue, upper and lower gums, hard and soft palates, floor of mouth, retromolar region, or inside of cheek), histologic forms (that can be carcinoma, sarcoma, lymphoma, melanoma or cylindroma) and clinical outcomes (good or poor prognosis). However, more than 50% of these cancer phenotypes express a mutation at TP53 gene while in the other 50% of cases; the TP53 protein pathway is often partially inactivated. In cancerous tissues, particularly in oral squamous cells, the loss of function at TP53 gene is associated with three molecular causes: (1) The genotoxic effect of risk factors such as alcohol abuse, tobacco smoking or betel nut chewing, (2) The inhibitory effect of the TP53 antagonist genes such as MDM2, or (3) The action of oncoproteins of high-risk human papillomavirus (HPV). This paper attempts firstly to make an exhaustive review of TP53 gene signalling pathways in normal and stressed cells, and secondly to describe in oral cancers the genetic events that occur at different steps of carcinogenesis after a loss of function in TP53 encoded protein.","PeriodicalId":88269,"journal":{"name":"Journal of molecular and genetic medicine : an international journal of biomedical research","volume":"15 1","pages":"1-11"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of molecular and genetic medicine : an international journal of biomedical research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37421/1747-0862.2021.15.504","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

Oral cancers are heterogeneous group of tumors in topography (they can be localized at on the lips, tongue, upper and lower gums, hard and soft palates, floor of mouth, retromolar region, or inside of cheek), histologic forms (that can be carcinoma, sarcoma, lymphoma, melanoma or cylindroma) and clinical outcomes (good or poor prognosis). However, more than 50% of these cancer phenotypes express a mutation at TP53 gene while in the other 50% of cases; the TP53 protein pathway is often partially inactivated. In cancerous tissues, particularly in oral squamous cells, the loss of function at TP53 gene is associated with three molecular causes: (1) The genotoxic effect of risk factors such as alcohol abuse, tobacco smoking or betel nut chewing, (2) The inhibitory effect of the TP53 antagonist genes such as MDM2, or (3) The action of oncoproteins of high-risk human papillomavirus (HPV). This paper attempts firstly to make an exhaustive review of TP53 gene signalling pathways in normal and stressed cells, and secondly to describe in oral cancers the genetic events that occur at different steps of carcinogenesis after a loss of function in TP53 encoded protein.
口腔癌和口腔癌中TP53基因信号通路及蛋白与MDM2和HPV的相互作用回顾
口腔癌在地形(可局限于唇部、舌部、上下牙龈、软硬腭、口腔底、臼齿后区或脸颊内侧)、组织学形式(可为癌、肉瘤、淋巴瘤、黑色素瘤或柱状瘤)和临床结果(预后好坏)上均属于异质性肿瘤。然而,超过50%的这些癌症表型表达TP53基因突变,而在另外50%的病例中;TP53蛋白通路通常部分失活。在癌组织中,特别是口腔鳞状细胞中,TP53基因功能的丧失与三个分子原因有关:(1)酗酒、吸烟或嚼槟榔等危险因素的遗传毒性作用,(2)TP53拮抗剂基因MDM2的抑制作用,或(3)高危人乳头瘤病毒(HPV)癌蛋白的作用。本文首先对正常细胞和应激细胞中的TP53基因信号通路进行了详尽的综述,其次描述了口腔癌中TP53编码蛋白功能丧失后在癌变的不同步骤中发生的遗传事件。
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