Wan Xiao, Li Zhaohui, Ye Hua, Cui Zhanfeng
Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, OX3 7DQ, UK.
Biotechnol Lett. 2016 Aug;38(8):1389-95. doi: 10.1007/s10529-016-2035-1. Epub 2016 May 11.
To build an in vitro-perfused, three-dimensional (3D) spheroid model based on the TissueFlex system for anti-cancer drug efficacy testing in order to mimic avascular micro-tissues with inherent O2, nutrient and metabolite gradients, and to provide a more accurate prediction of drug toxicity and efficacy than traditional in vitro tumour models in conventional static culture well plates.
The perfused cancer spheroid model showed higher cell viability and increased diameter of spheroids over a relatively long culture period (17 days). Three anti-cancer drugs with different cytotoxic mechanisms were tested. In perfusion, lower cytotoxicity was observed for traditional cytotoxic drug 5-fluorouracil and microtubule-interfering, paclitaxel, showed greater interruption of spheroid integrity. For the hypoxic-dependent drug, tirapazamine, there was no significant difference observed between static and perfusion cultures.
The perfusion culture provides a better homeostasis for cancer cell growth in a more controllable working platform for long-term drug testing.
基于TissueFlex系统构建一种体外灌注的三维(3D)球体模型,用于抗癌药物疗效测试,以模拟具有内在氧气、营养物质和代谢物梯度的无血管微组织,并比传统静态培养孔板中的体外肿瘤模型更准确地预测药物毒性和疗效。
灌注的癌症球体模型在相对较长的培养期(17天)内显示出更高的细胞活力和球体直径增加。测试了三种具有不同细胞毒性机制的抗癌药物。在灌注过程中,观察到传统细胞毒性药物5-氟尿嘧啶的细胞毒性较低,而微管干扰剂紫杉醇对球体完整性的破坏更大。对于缺氧依赖性药物替拉扎明,静态培养和灌注培养之间未观察到显著差异。
灌注培养在更可控的工作平台上为癌细胞生长提供了更好的稳态,用于长期药物测试。