Division of Cancer Treatment and Diagnosis, National Cancer Institute, Rockville, MD, USA.
Sirnaomics, Inc., Gaithersburg, MD, USA.
SLAS Discov. 2021 Dec;26(10):1298-1314. doi: 10.1177/24725552211038362. Epub 2021 Nov 12.
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.
恶性肿瘤是由恶性细胞、血管细胞、包括周细胞和癌相关成纤维细胞在内的结构间充质细胞、浸润免疫细胞等组成的复杂组织,统称为肿瘤基质。肿瘤中的基质细胞数量通常远远多于恶性细胞。所有这些细胞类型之间的物理联系对肿瘤的生长、存活和对治疗的反应至关重要。大多数用于癌症药物发现和精准医学验证的基于细胞的筛选都是将恶性细胞作为单层细胞、嵌入基质中或作为悬浮的球体进行分离使用。使用多种细胞系进行中高通量筛选需要可扩展、可重复、稳健的基于细胞的测定方法。复杂球体包括恶性细胞和两种正常细胞类型,即人脐静脉内皮细胞和高度可塑的间充质干细胞,它们能迅速适应恶性细胞的微环境。用人胰腺导管腺癌细胞系 K24384-001-R 探索了在 96 孔板格式中复杂球体的结构和对抗癌药物的反应。我们描述了复杂球体测定方法的开发以及复杂球体随时间的生长和结构。随后,我们成功地将其微型化为 384 孔格式,并在高通量筛选中实现了稳健的性能。该复杂球体测定法还在 10 种已建立的胰腺细胞系中得到了进一步验证。通过同时包含人类基质和肿瘤成分,复杂球体可能为体内肿瘤反应提供更好的模型。