Complex Tumor Spheroids, a Tissue-Mimicking Tumor Model, for Drug Discovery and Precision Medicine

被引:12
作者
Kaur, Gurmeet [1 ]
Evans, David M. [2 ]
Teicher, Beverly A. [1 ]
Coussens, Nathan P. [3 ]
机构
[1] NCI, Div Canc Treatment & Diag, Rockville, MD USA
[2] Sirnaomics Inc, Gaithersburg, MD USA
[3] Frederick Natl Lab Canc Res, Appl & Dev Res Directorate, Mol Pharmacol Labs, 1050 Boyles St, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
high-throughput screening; spheroid; in vitro tumor model; malignant cells; precision medicine; assay; oncology; preclinical; therapeutics; anticancer drugs; PROTEIN EXPRESSION; CELL-LINES; CANCER; STROMA; MECHANISMS; RESISTANCE; CULTURES; BIOLOGY; SYSTEMS;
D O I
10.1177/24725552211038362
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Malignant tumors are complex tissues composed of malignant cells, vascular cells, structural mesenchymal cells including pericytes and carcinoma-associated fibroblasts, infiltrating immune cells, and others, collectively called the tumor stroma. The number of stromal cells in a tumor is often much greater than the number of malignant cells. The physical associations among all these cell types are critical to tumor growth, survival, and response to therapy. Most cell-based screens for cancer drug discovery and precision medicine validation use malignant cells in isolation as monolayers, embedded in a matrix, or as spheroids in suspension. Medium- and high-throughput screening with multiple cell lines requires a scalable, reproducible, robust cell-based assay. Complex spheroids include malignant cells and two normal cell types, human umbilical vein endothelial cells and highly plastic mesenchymal stem cells, which rapidly adapt to the malignant cell microenvironment. The patient-derived pancreatic adenocarcinoma cell line, K24384-001-R, was used to explore complex spheroid structure and response to anticancer agents in a 96-well format. We describe the development of the complex spheroid assay as well as the growth and structure of complex spheroids over time. Subsequently, we demonstrate successful assay miniaturization to a 384-well format and robust performance in a high-throughput screen. Implementation of the complex spheroid assay was further demonstrated with 10 well-established pancreatic cell lines. By incorporating both human stromal and tumor components, complex spheroids might provide an improved model for tumor response in vivo.
引用
收藏
页码:1298 / 1314
页数:17
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