Using 3D-bioprinted models to study pediatric neural crest-derived tumors

被引:3
|
作者
Quinn, Colin H. [1 ]
Beierle, Andee M. [2 ]
Julson, Janet R. [1 ]
Erwin, Michael E. [1 ]
Alrefai, Hasan [2 ]
Markert, Hooper R. [1 ]
Stewart, Jerry E. [1 ]
Hutchins, Sara Claire [3 ]
V. Bownes, Laura [1 ]
Aye, Jamie M. [3 ]
Mroczek-Musulman, Elizabeth [4 ]
Hicks, Patricia H. [4 ]
Yoon, Karina J. [5 ]
Willey, Christopher D. [2 ]
Beierle, Elizabeth A. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Surg, Div Pediat Surg, Birmingham, AL 35205 USA
[2] Univ Alabama Birmingham, Dept Radiat Oncol, Birmingham, AL 35205 USA
[3] Univ Alabama Birmingham, Dept Pediat, Div Pediat Hematol Oncol, Birmingham, AL 35233 USA
[4] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35233 USA
[5] Univ Alabama Birmingham, Dept Pharmacol & Toxicol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
3D bioprinting; Neuroblastoma; Neuroendocrine; Pediatrics; Targeted therapy; Patient-derived xenografts; HIGH-RISK NEUROBLASTOMA; PHENOTYPES; HYPOXIA;
D O I
10.18063/ijb.723
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The use of three-dimensional (3D) bioprinting has remained at the forefront of tissue engineering and has recently been employed for generating bioprinted solid tumors to be used as cancer models to test therapeutics. In pediatrics, neural crest-derived tumors are the most common type of extracranial solid tumors. There are only a few tumor-specific therapies that directly target these tumors, and the lack of new therapies remains detrimental to improving the outcomes for these patients. The absence of more efficacious therapies for pediatric solid tumors, in general, may be due to the inability of the currently employed preclinical models to recapitulate the solid tumor phenotype. In this study, we utilized 3D bioprinting to generate neural crest-derived solid tumors. The bioprinted tumors consisted of cells from established cell lines and patient-derived xenograft tumors mixed with a 6% gelatin/1% sodium alginate bioink. The viability and morphology of the bioprints were analyzed via bioluminescence and immunohisto chemistry, respectively. We compared the bioprints to traditional two-dimensional (2D) cell culture under conditions such as hypoxia and therapeutics. We successfully produced viable neural crest-derived tumors that retained the histology and immunostaining characteristics of the original parent tumors. The bioprinted tumors propagated in culture and grew in orthotopic murine models. Furthermore, compared to cells grown in traditional 2D culture, the bioprinted tumors were resistant to hypoxia and chemotherapeutics, suggesting that the bioprints exhibited a phenotype that is consistent with that seen clinically in solid tumors, thus potentially making this model superior to traditional 2D culture for preclinical investigations. Future applications of this technology entail the potential to rapidly print pediatric solid tumors for use in high -throughput drug studies, expediting the identification of novel, individualized therapies.
引用
收藏
页码:115 / 128
页数:14
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