Design and analysis of a squamous cell carcinoma in vitro model system

被引:30
作者
Brauchle, Eva [1 ,2 ,3 ,4 ]
Johannsen, Hannah [1 ]
Nolan, Samantha [1 ]
Thude, Sibylle [1 ]
Schenke-Layland, Katja [1 ,2 ,3 ]
机构
[1] Fraunhofer Inst Interfacial Engn & Biotechnol IGB, Dept Cell & Tissue Engn, D-70569 Stuttgart, Germany
[2] Univ Tubingen, Univ Womens Hosp Tubingen, D-72076 Tubingen, Germany
[3] Univ Tubingen, Interuniv Ctr Med Technol IZST, D-72076 Tubingen, Germany
[4] Univ Stuttgart, Inst Interfacial Engn & Plasma Technol IGVP, D-70569 Stuttgart, Germany
关键词
Co-culture; Epithelium; In vitro test; Organ culture; Keratinocyte; MICRO-RAMAN SPECTROSCOPY; NONMELANOMA SKIN-CANCER; 3-DIMENSIONAL MODEL; DIFFERENTIATION; VIVO; TOOL;
D O I
10.1016/j.biomaterials.2013.06.016
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Tissue-engineered skin equivalents based on primary isolated fibroblasts and keratinocytes have been shown to be useful tools for functional in vitro tests, including toxicological screenings and drug development. In this study, a commercially available squamous cell carcinoma (SCC) cell line SCC-25 was introduced into epidermal and full-thickness skin equivalents to generate human-based disease-in-a-dish model systems. Interestingly, when cultured either in the epidermis or dermis of full-thickness skin equivalents, SCC-25 cells formed hyper-keratinized tumor cell nests, a phenomenon that is frequently seen in the skin of patients afflicted with SCC. Raman spectroscopy was employed for the label-free cell phenotype characterization within the engineered skin equivalents and revealed the presence of differential protein patterns in keratinocytes and SCC-25 cells. To conclude, the here presented SSC disease-in-a-dish approaches offer the unique opportunity to model SSC in human skin in vitro, which will allow further insight into SSC disease progression, and the development of therapeutic strategies. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7401 / 7407
页数:7
相关论文
共 40 条
[1]
[Anonymous], 1989, MULTIVARIATE CALIBRA
[2]
FOURIER-TRANSFORM RAMAN AND INFRARED VIBRATIONAL STUDY OF HUMAN SKIN - ASSIGNMENT OF SPECTRAL BANDS [J].
BARRY, BW ;
EDWARDS, HGM ;
WILLIAMS, AC .
JOURNAL OF RAMAN SPECTROSCOPY, 1992, 23 (11) :641-645
[3]
Non-melanoma skin cancer: what drives tumor development and progression? [J].
Boukamp, P .
CARCINOGENESIS, 2005, 26 (10) :1657-1667
[4]
Raman spectroscopy in biomedicine - non-invasive in vitro analysis of cells and extracellular matrix components in tissues [J].
Brauchle, Eva ;
Schenke-Layland, Katja .
BIOTECHNOLOGY JOURNAL, 2013, 8 (03) :288-297
[5]
Caspers PJ, 1998, BIOSPECTROSCOPY, V4, pS31, DOI 10.1002/(SICI)1520-6343(1998)4:5+<S31::AID-BSPY4>3.0.CO
[6]
2-M
[7]
An in vitro three-dimensional model of primary human cutaneous squamous cell carcinoma [J].
Commandeur, Suzan ;
de Gruijl, Frank R. ;
Willemze, Rein ;
Tensen, Cornelis P. ;
El Ghalbzouri, Abdoelwaheb .
EXPERIMENTAL DERMATOLOGY, 2009, 18 (10) :849-856
[8]
Effect of fibroblasts on epidermal regeneration [J].
El-Ghalbzouri, A ;
Gibbs, S ;
Lamme, E ;
Van Blitterswijk, CA ;
Ponec, M .
BRITISH JOURNAL OF DERMATOLOGY, 2002, 147 (02) :230-243
[9]
EPIDERMAL DIFFERENTIATION - THE BARE ESSENTIALS [J].
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :2807-2814
[10]
The risk of progression to invasive disease [J].
Glogau, RG .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (01) :S23-S24