An in vitro three-dimensional model of primary human cutaneous squamous cell carcinoma

被引:37
作者
Commandeur, Suzan [1 ]
de Gruijl, Frank R. [1 ]
Willemze, Rein [1 ]
Tensen, Cornelis P. [1 ]
El Ghalbzouri, Abdoelwaheb [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Dermatol, NL-2300 RC Leiden, Netherlands
关键词
organotypic; explant; skin cancer; skin model; squamous cell carcinoma; HUMAN-SKIN; BASEMENT-MEMBRANE; GENE-EXPRESSION; EPIDERMOLYSIS-BULLOSA; TYROSINE KINASE; KAPPA-B; TUMORS; LINES; INVASION; COLLAGEN;
D O I
10.1111/j.1600-0625.2009.00856.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Squamous cell carcinomas (SCC) represent a substantial clinical problem because of increases, frequent recurrences and successive de novo tumors, especially in organ transplant recipients. To improve upon the current surgical and other non-selective therapies, a validated organotypic in vitro model of primary human SCC needs to be developed. Such a model will have obvious advantages over current cell line and animal based approaches, and may render the latter partly obsolete. In a first approach, an explant technique of primary SCC biopsies onto dermal constructs was used to emulate tumor expansion in an in vitro model. Histological analysis revealed the formation of nests of squamous cells, mimicking an invasive morphological feature of primary SCC. Immunohistochemical analysis comprised an array of markers characteristic of keratinocyte (hyper) proliferation (K6, K16, K17 and Ki67), differentiation (K1, K10 and involucrin), basement membrane (collagen types IV and VII, integrins alpha(6) and beta(4) and laminin 332) and SCC (K4, K13 and Axl). The generated human SCC models displayed disturbed differentiation and keratins associated with hyperproliferation, but a low frequency of Ki67 positive cells. Basement membrane composition of the in vitro SCC model resembled that of normal skin. These results show for the first time that in vitro modelling of three-dimensional growth of primary cutaneous human SCC is feasible. This model may provide a platform to develop refined preventive and curative treatments and thereby gain understanding of SCC pathogenesis.
引用
收藏
页码:849 / 856
页数:8
相关论文
共 42 条
[1]   UVB induction of epithelial tumors in human skin using a RAG-1 mouse xenograft model [J].
Atillasoy, ES ;
Elenitsas, R ;
Sauter, ER ;
Soballe, PW ;
Herlyn, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1997, 109 (06) :704-709
[2]   The risk of skin cancer in renal transplant recipients in Queensland, Australia [J].
Bavinck, JNB ;
Hardie, DR ;
Green, A ;
Cutmore, S ;
MacNaught, A ;
OSullivan, B ;
Siskind, V ;
VanDerWoude, FJ ;
Hardie, IR .
TRANSPLANTATION, 1996, 61 (05) :715-721
[3]   Gene expression of differentiation-specific keratins in oral epithelial dysplasia and squamous cell carcinoma [J].
Bloor, BK ;
Seddon, SV ;
Morgan, PR .
ORAL ONCOLOGY, 2001, 37 (03) :251-261
[4]   TRANSGENIC MICE AND SQUAMOUS MULTISTAGE SKIN CARCINOGENESIS [J].
BROWN, K ;
BALMAIN, A .
CANCER AND METASTASIS REVIEWS, 1995, 14 (02) :113-124
[5]  
Chang C, 2001, TRENDS CELL BIOL, V11, pS37, DOI 10.1016/S0962-8924(01)82222-4
[6]   NF-κB blockade and oncogenic Ras trigger invasive human epidermal neoplasia [J].
Dajee, M ;
Lazarov, M ;
Zhang, JY ;
Cai, T ;
Green, CL ;
Russell, AJ ;
Marinkovich, MP ;
Tao, SY ;
Lin, Q ;
Kubo, Y ;
Khavari, PA .
NATURE, 2003, 421 (6923) :639-643
[7]   Predictions of skin cancer incidence in the Netherlands up to 2015 [J].
de Vries, E ;
van de Poll-Franse, LV ;
Louwman, WJ ;
de Gruijl, FR ;
Coebergh, JWW .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 152 (03) :481-488
[8]  
Eicher SA, 1996, CLIN CANCER RES, V2, P1659
[9]   Fibroblasts facilitate re-epithelialization in wounded human skin equivalents [J].
El Ghalbzouri, A ;
Hensbergen, P ;
Gibbs, S ;
Kempenaar, J ;
van der Schors, R ;
Ponec, M .
LABORATORY INVESTIGATION, 2004, 84 (01) :102-112
[10]   Recessive epidermolysis bullosa simplex phenotype reproduced in vitro -: Ablation of keratin 14 is partially compensated by keratin 17 [J].
El Ghalbzouri, A ;
Jonkman, M ;
Kempenaar, J ;
Ponec, M .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (05) :1771-1779