Non-Animal Models in Dermatological Research

被引:36
作者
Dellambra, Elena [1 ,4 ]
Odorisio, Teresa [1 ,4 ]
D'Arcangelo, Daniela [2 ,4 ]
Failla, Cristina M. [3 ,4 ]
Facchiano, Antonio [2 ,4 ]
机构
[1] IRCCS, IDI, Lab Mol & Cell Biol, Rome, Italy
[2] IRCCS, IDI, Lab Mol Oncol, Rome, Italy
[3] IRCCS, IDI, Lab Expt Immunol, Via Moriti di Creta 104, I-00167 Rome, Italy
[4] IRCCS, IDI, Working Grp ALMA, Rome, Italy
关键词
IN-VITRO MODEL; ADVANCED GLYCATION ENDPRODUCTS; HUMAN-MELANOMA PROGRESSION; HUMAN SKIN EQUIVALENT; DIABETIC FOOT ULCERS; WOUND-HEALING MODEL; HUMAN PROTEIN ATLAS; HUMAN CELL-LINES; TEST H-CLAT; RECONSTRUCTED-SKIN;
D O I
10.14573/altex.1808022
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Despite being widely used for basic and preclinical studies in dermatology, available animal models only partly recapitulate human skin features, often leading to disappointing outputs when preclinical results are translated to the clinic. Therefore, the need to develop alternative, non-animal models is widely recognized to more closely recapitulate human skin pathophysiology and to address the pressing ethical demand to reduce the number of animals used for research purposes, following the globally accepted 3Rs principle (Replacement, Reduction, and Refinement). Skin is the outermost organ of the body, and is, as such, easily accessible. Different skin cell types can be propagated in vitro, and skin can be reconstructed for therapeutic transplantation as well as for in vitro modelling of pathophysiological conditions. Bio-engineered skin substitutes have been developed and have evolved from elementary to complex systems, more and more closely resembling complete skin architecture and biological responses. In silico analyses take advantage of the huge amount of data already available from human studies to identify and model molecular pathways involved in skin pathophysiology without further animal testing. The present review recapitulates the available non-animal models for dermatological research and sheds light on their prospective technological evolution.
引用
收藏
页码:177 / 202
页数:26
相关论文
共 281 条
[11]   Intrahepatic Xenograft of Cutaneous T-Cell Lymphoma Cell Lines A Useful Model for Rapid Biological and Therapeutic Evaluation [J].
Andrique, Laetitia ;
Poglio, Sandrine ;
Prochazkova-Carlotti, Martina ;
Kadin, Marshall Edward ;
Giese, Alban ;
Idrissi, Yamina ;
Beylot-Barry, Marie ;
Merlio, Jean-Philippe ;
Chevret, Edith .
AMERICAN JOURNAL OF PATHOLOGY, 2016, 186 (07) :1775-1785
[12]  
[Anonymous], 2017, BTS BIOENG, DOI DOI 10.3390/BIOENGINEERING4030066
[13]   Development of an in vitro skin sensitization test using human cell lines: The human Cell Line Activation Test (h-CLAT) I. Optimization of the h-CLAT protocol [J].
Ashikaga, T ;
Yoshida, Y ;
Hirota, M ;
Yoneyama, K ;
Itagaki, H ;
Sakaguchi, H ;
Miyazawa, M ;
Ito, Y ;
Suzuki, H ;
Toyoda, H .
TOXICOLOGY IN VITRO, 2006, 20 (05) :767-773
[14]   RECONSTRUCTION OF SIMPLIFIED SKIN - CONTROL OF FABRICATION [J].
ASSELINEAU, D ;
PRUNIERAS, M .
BRITISH JOURNAL OF DERMATOLOGY, 1984, 111 :219-222
[15]   Skin and hair on-a-chip: in vitro skin models versus ex vivo tissue maintenance with dynamic perfusion [J].
Atac, Beren ;
Wagner, Ilka ;
Horland, Reyk ;
Lauster, Roland ;
Marx, Uwe ;
Tonevitsky, Alexander G. ;
Azar, Reza P. ;
Lindner, Gerd .
LAB ON A CHIP, 2013, 13 (18) :3555-3561
[16]   A systems approach reveals distinct metabolic strategies among the NCI-60 cancer cell lines [J].
Aurich, Maike K. ;
Fleming, Ronan M. T. ;
Thiele, Ines .
PLOS COMPUTATIONAL BIOLOGY, 2017, 13 (08) :e1005698
[17]   Animal models of skin disease for drug discovery [J].
Avci, Pinar ;
Sadasivam, Magesh ;
Gupta, Asheesh ;
De Melo, Wanessa C. M. A. ;
Huang, Ying-Ying ;
Yin, Rui ;
Chandran, Rakkiyappan ;
Kumar, Raj ;
Otufowora, Ayodeji ;
Nyame, Theodore ;
Hamblin, Michael R. .
EXPERT OPINION ON DRUG DISCOVERY, 2013, 8 (03) :331-355
[18]  
Ayata Raif Eren, 2014, Biores Open Access, V3, P197, DOI 10.1089/biores.2014.0022
[19]   In Silico Analysis Validates Proteomic Findings of Formalin-fixed Paraffin Embedded Cutaneous Squamous Cell Carcinoma Tissue [J].
Azimi, Ali ;
Kaufman, Kimberley L. ;
Ali, Marina ;
Kossard, Steven ;
Fernandez-Penas, Pablo .
CANCER GENOMICS & PROTEOMICS, 2016, 13 (06) :453-465
[20]   The HtrA1 serine protease is down-regulated during human melanoma progression and represses growth of metastatic melanoma cells [J].
Baldi, A ;
De Luca, A ;
Morini, M ;
Battista, T ;
Felsani, A ;
Baldi, F ;
Catricalà, C ;
Amantea, A ;
Noonan, DM ;
Albini, A ;
Natali, PG ;
Lombardi, D ;
Paggi, MG .
ONCOGENE, 2002, 21 (43) :6684-6688