The 4-NQO mouse model: An update on a well-established in vivo model of oral carcinogenesis

被引:21
作者
Bouaoud, J. [1 ,2 ]
De Souza, G. [1 ]
Darido, C. [3 ,4 ]
Tortereau, A. [5 ]
Elkabets, M. [6 ]
Bertolus, C. [2 ]
Saintigny, P. [1 ,7 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, INSERM 1052, Ctr Leon Berard,Ctr Rech Cancerol Lyon,CNRS 5286, Lyon, France
[2] Sorbonne Univ, Hop Pitie Salpetriere, Assistance Publ Hop Paris, Dept Maxillofacial Surg, Paris, France
[3] Peter MacCallum Canc Ctr, Melbourne, Vic, Australia
[4] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic, Australia
[5] Univ Lyon, Dept Pathol, VetAgro Sup, Marcy Letoile, France
[6] Ben Gurion Univ Negev, Shraga Segal Dept Microbiol Immunol & Genet, Beer Sheva, Israel
[7] Ctr Leon Berard, Dept Med Oncol, Lyon, France
来源
CARCINOGEN-DRIVEN MOUSE MODELS OF ONCOGENESIS | 2021年 / 163卷
关键词
SQUAMOUS-CELL CARCINOMA; UPPER AERODIGESTIVE TRACT; GROWTH-FACTOR RECEPTOR; ANIMAL-MODELS; 4-NITROQUINOLINE; 1-OXIDE; CHEMICAL CARCINOGENESIS; IMMUNE-SYSTEM; ESOPHAGEAL CARCINOGENESIS; HISTORICAL-PERSPECTIVE; MUCOSAL CARCINOGENESIS;
D O I
10.1016/bs.mcb.2020.09.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The early detection and management of oral premalignant lesions (OPMDs) improve their outcomes. Animal models that mimic histological and biological processes of human oral carcinogenesis may help to improve the identification of OPMD at-risk of progression into oral squamous cell carcinoma and to develop preventive strategies for the entire field of cancerization. No animal model is perfectly applicable for investigating human oral carcinogenesis. However, the 4-nitroquinoline 1-oxide (4-NQO) mouse model is well established and mimics several morphological, histological, genomic and molecular features of human oral carcinogenesis. Some of the reasons for the success of this model include its reproducible experimental conditions with limited variation, the possibility of realizing longitudinal studies with invasive intervention or gene manipulation, and sample availability for all stages of oral carcinogenesis, especially premalignant lesions. Moreover, the role of histological and molecular alterations in the field of cancerization (i.e., macroscopically healthy mucosa exposed to a carcinogen) during oral carcinogenesis can be easily explored using this model. In this review, we discuss the advantages and drawbacks of this model for studying human oral carcinogenesis. In summary, the 4-NQO-induced murine oral cancer model is relevant for investigating human oral carcinogenesis, including the immune microenvironment, and for evaluating therapeutic and chemoprevention agents.
引用
收藏
页码:197 / 229
页数:33
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