Molecular Imaging Center, National Institute of Radiological Sciences, Anagawa, Chiba 263-8555, Japan.
Molecular Imaging Center, National Institute of Radiological Sciences, Anagawa, Chiba 263-8555, Japan.
Biomaterials. 2015 May;51:278-289. doi: 10.1016/j.biomaterials.2015.02.008. Epub 2015 Feb 21.
Anti-cancer drug development typically utilizes high-throughput screening with two-dimensional (2D) cell culture. However, 2D culture induces cellular characteristics different from tumors in vivo, resulting in inefficient drug development. Here, we report an innovative high-throughput screening system using nanoimprinting 3D culture to simulate in vivo conditions, thereby facilitating efficient drug development. We demonstrated that cell line-based nanoimprinting 3D screening can more efficiently select drugs that effectively inhibit cancer growth in vivo as compared to 2D culture. Metabolic responses after treatment were assessed using positron emission tomography (PET) probes, and revealed similar characteristics between the 3D spheroids and in vivo tumors. Further, we developed an advanced method to adopt cancer cells from patient tumor tissues for high-throughput drug screening with nanoimprinting 3D culture, which we termed Cancer tissue-Originated Uniformed Spheroid Assay (COUSA). This system identified drugs that were effective in xenografts of the original patient tumors. Nanoimprinting 3D spheroids showed low permeability and formation of hypoxic regions inside, similar to in vivo tumors. Collectively, the nanoimprinting 3D culture provides easy-handling high-throughput drug screening system, which allows for efficient drug development by mimicking the tumor environment. The COUSA system could be a useful platform for drug development with patient cancer cells.
抗癌药物的开发通常采用二维(2D)细胞培养的高通量筛选。然而,2D 培养会诱导出与体内肿瘤不同的细胞特性,从而导致药物开发效率低下。在这里,我们报告了一种使用纳米压印 3D 培养来模拟体内条件的创新高通量筛选系统,从而促进有效的药物开发。我们证明,与 2D 培养相比,基于细胞系的纳米压印 3D 筛选可以更有效地选择在体内有效抑制肿瘤生长的药物。使用正电子发射断层扫描(PET)探针评估治疗后的代谢反应,揭示了 3D 球体和体内肿瘤之间的相似特征。此外,我们开发了一种先进的方法,采用患者肿瘤组织中的癌细胞进行高通量药物筛选纳米压印 3D 培养,我们称之为癌症组织起源均匀球体分析(COUSA)。该系统鉴定出了对原始患者肿瘤异种移植物有效的药物。纳米压印 3D 球体表现出低渗透性和内部缺氧区域的形成,与体内肿瘤相似。总之,纳米压印 3D 培养提供了易于处理的高通量药物筛选系统,通过模拟肿瘤环境实现高效的药物开发。COUSA 系统可以成为使用患者癌细胞进行药物开发的有用平台。