Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8-expressing transgenic mice

被引:45
作者
Casanova, ML
Bravo, A
Martínez-Palacio, J
Fernández-Aceñero, MJ
Villanueva, C
Larcher, F
Conti, CJ
Jorcano, JL
机构
[1] CIEMAT, Epithelial Damage Repair & Tissue Engn, E-28040 Madrid, Spain
[2] Univ Santiago de Compostela, Fac Vet, Dept Anim Pathol, Lugo, Spain
[3] Univ Texas, MD Anderson Canc Ctr, Smithville, TX USA
[4] Hosp Gen Mostoles, Madrid, Spain
关键词
cutaneous cancer; epithelial dysplastic changes; ectopic keratin expression; neoplastic diseases;
D O I
10.1096/fj.04-1683fje
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Keratins K8 and K18 are the major components of the intermediate filament cytoskeleton of simple epithelia. Increased levels of these keratins have been associated with invasive growth and progression to malignancy in different types of human and murine epithelial tumors ( including skin tumors), and even in tumors from nonepithelial origin. However, it has not yet clarified whether K8/K18 expression in tumors is cause or consequence of malignancy. Given the increasing incidence of epidermal cancer in humans (40% of all tumors diagnosed), we generated a mouse model to examine the role of simple epithelium keratins in the establishment and progression of human skin cancer. Transgenic mice expressing human K8 in the epidermis showed severe epidermal and hair follicle dysplasia with concomitant alteration in epidermal differentiation markers. The severity of the skin phenotype of these transgenic mice increases with age, leading to areas of preneoplastic transformation. Skin carcinogenesis assays showed a dramatic increase in the progression of papillomas toward malignancy in transgenic animals. These results support the idea that K8 alters the epidermal cell differentiation, favors the neoplastic transformation of cells, and is ultimately responsible of the invasive behavior of transformed epidermal cells leading of conversion of benign to malignant tumors.
引用
收藏
页码:1556 / +
页数:23
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