Chemically induced skin carcinogenesis: Updates in experimental models (Review)

被引:95
作者
Neagu, Monica [1 ,2 ]
Caruntu, Constantin [3 ,4 ]
Constantin, Carolina [1 ]
Boda, Daniel [4 ]
Zurac, Sabina [5 ]
Spandidos, Demetrios A. [6 ]
Tsatsakis, Aristidis M. [7 ]
机构
[1] Victor Babes Natl Inst Pathol, Bucharest 050096, Romania
[2] Univ Bucharest, Fac Biol, Bucharest 76201, Romania
[3] Carol Davila Univ Med & Pharm, Dept Physiol, 8 Blvd Eroii Sanit, Bucharest 050474, Romania
[4] Prof N Paulescu Natl Inst Diabet, Dept Dermatol, Nutr & Metab Dis, Bucharest 79811, Romania
[5] Colentina Clin Hosp, Dept Pathol, Bucharest 72202, Romania
[6] Univ Crete, Sch Med, Lab Clin Virol, Iraklion 71409, Greece
[7] Univ Crete, Sch Med, Dept Forens Sci & Toxicol, Iraklion 71003, Greece
关键词
skin cancer; chemically induced carcinogenesis; mouse model; TO-MESENCHYMAL TRANSITION; MOUSE SKIN; IN-VIVO; TUMOR PROMOTION; STEM-CELLS; MOLECULAR-MECHANISMS; CANCER; SENCAR; INFLAMMATION; INHIBITION;
D O I
10.3892/or.2016.4683
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Skin cancer is one of the most common malignancies affecting humans worldwide, and its incidence is rapidly increasing. The study of skin carcinogenesis is of major interest for both scientific research and clinical practice and the use of in vivo systems may facilitate the investigation of early alterations in the skin and of the mechanisms involved, and may also lead to the development of novel therapeutic strategies for skin cancer. This review outlines several aspects regarding the skin toxicity testing domain in mouse models of chemically induced skin carcinogenesis. There are important strain differences in view of the histological type, development and clinical evolution of the skin tumor, differences reported decades ago and confirmed by our hands-on experience. Using mouse models in preclinical testing is important due to the fact that, at the molecular level, common mechanisms with human cutaneous tumorigenesis are depicted. These animal models resemble human skin cancer development, in that genetic changes caused by carcinogens and pro-inflammatory cytokines, and simultaneous inflammation sustained by pro-inflammatory cytokines and chemokines favor tumor progression. Drugs and environmental conditions can be tested using these animal models. keeping in mind the differences between human and rodent skin physiology.
引用
收藏
页码:2516 / 2528
页数:13
相关论文
共 129 条
[1]   Multi-stage chemical carcinogenesis in mouse skin: Fundamentals and applications [J].
Abel, Erika L. ;
Angel, Joe M. ;
Kiguchi, Kaoru ;
DiGiovanni, John .
NATURE PROTOCOLS, 2009, 4 (09) :1350-1362
[2]  
Acunzo Mario, 2015, Adv Biol Regul, V57, P1, DOI 10.1016/j.jbior.2014.09.013
[3]   Inhibition of Mammalian Target of Rapamycin by Rapamycin Causes the Regression of Carcinogen-induced Skin Tumor Lesions [J].
Amornphimoltham, Panomwat ;
Leelahavanichkul, Kantima ;
Molinolo, Alfredo ;
Patel, Vyomesh ;
Gutkind, J. Silvio .
CLINICAL CANCER RESEARCH, 2008, 14 (24) :8094-8101
[4]  
[Anonymous], 2011, INTERNAL MED
[5]  
[Anonymous], TOXICOL APPL PHARM
[6]  
[Anonymous], 2011, ROM MED J
[7]   2-STAGE SKIN CARCINOGENESIS IN SENSITIVE AND RESISTANT MOUSE STRAINS [J].
ASHMAN, LK ;
MURRAY, AW ;
COOK, MG ;
KOTLARSKI, I .
CARCINOGENESIS, 1982, 3 (01) :99-102
[8]  
Bassi DE, 2007, CARCINOGEN INDUCED A
[9]   P53 and the pathogenesis of skin cancer [J].
Benjamin, Cara L. ;
Ananthaswamy, Honnavara N. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 224 (03) :241-248
[10]   THY-1 ANTIGEN-BEARING DENDRITIC CELLS POPULATE MURINE EPIDERMIS [J].
BERGSTRESSER, PR ;
TIGELAAR, RE ;
DEES, JH ;
STREILEIN, JW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (03) :286-288