Tissue-engineered 3D melanoma model with blood and lymphatic capillaries for drug development

被引:57
|
作者
Bourland, Jennifer [1 ,2 ,3 ]
Fradette, Julie [1 ,2 ,3 ]
Auger, Francois A. [1 ,2 ,3 ]
机构
[1] Univ Laval, Ctr Rech Organogenese Expt, LOEX, Quebec City, PQ, Canada
[2] Univ Laval, CHU Quebec, Res Ctr, Div Regenerat Med, Quebec City, PQ, Canada
[3] Univ Laval, Fac Med, Dept Surg, Quebec City, PQ, Canada
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
IN-VITRO RECONSTRUCTION; SKIN SUBSTITUTE; MICROVASCULAR NETWORK; CELLS; THERAPY; REVEALS; CULTURE; MICROENVIRONMENT; IDENTIFICATION; PROLIFERATION;
D O I
10.1038/s41598-018-31502-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While being the rarest skin cancer, melanoma is also the deadliest. To further drug discovery and improve clinical translation, new human cell-based in vitro models are needed. Our work strives to mimic the melanoma microenvironment in vitro as an alternative to animal testing. We used the self-assembly method to produce a 3D human melanoma model exempt of exogenous biomaterial. This model is based on primary human skin cells and melanoma cell lines while including a key feature for tumor progression: blood and lymphatic capillaries. Major components of the tumor microenvironment such as capillaries, human extracellular matrix, a stratified epidermis (involucrin, filaggrin) and basement membrane (laminin 332) are recapitulated in vitro. We demonstrate the persistence of CD31(+) blood and podoplanin(+)/LYVE-1(+) lymphatic capillaries in the engineered tissue. Chronic treatment with vemurafenib was applied to the model and elicited a dose-dependent response on proliferation and apoptosis, making it a promising tool to test new compounds in a human-like environment.
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页数:13
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