Centre for Microsystems and Photonics, Electronic and Electrical Engineering, University of Strathclyde, Glasgow, G1 1XW, UK.
Institute of Cancer Science, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G61 1QH, UK.
Sci Rep. 2018 Oct 2;8(1):14672. doi: 10.1038/s41598-018-33055-0.
Performing drug screening of tissue derived from cancer patient biopsies using physiologically relevant 3D tumour models presents challenges due to the limited amount of available cell material. Here, we present a microfluidic platform that enables drug screening of cancer cell-enriched multicellular spheroids derived from tumour biopsies, allowing extensive anticancer compound screening prior to treatment. This technology was validated using cell lines and then used to screen primary human prostate cancer cells, grown in 3D as a heterogeneous culture from biopsy-derived tissue. The technology enabled the formation of repeatable drug concentration gradients across an array of spheroids without external fluid actuation, delivering simultaneously a range of drug concentrations to multiple sized spheroids, as well as replicates for each concentration. As proof-of-concept screening, spheroids were generated from two patient biopsies and a panel of standard-of-care compounds for prostate cancer were tested. Brightfield and fluorescence images were analysed to provide readouts of spheroid growth and health, as well as drug efficacy over time. Overall, this technology could prove a useful tool for personalised medicine and future drug development, with the potential to provide cost- and time-reduction in the healthcare delivery.
由于可用于实验的细胞材料有限,利用与生理相关的 3D 肿瘤模型对取自癌症患者活检的组织进行药物筛选存在挑战。在这里,我们提出了一种微流控平台,可用于筛选源自肿瘤活检的富含癌细胞的多细胞球体的药物,从而在治疗前进行广泛的抗癌化合物筛选。该技术首先在细胞系中进行了验证,然后用于筛选源自活检组织的 3D 异质培养的原代人前列腺癌细胞。该技术可在无外部流体驱动的情况下,在一系列球体上形成可重复的药物浓度梯度,同时将一系列药物浓度输送到多个不同大小的球体,并为每个浓度提供重复样本。作为概念验证筛选,我们从两个患者的活检样本中生成了球体,并测试了一组用于前列腺癌的标准治疗化合物。通过分析明场和荧光图像,提供了关于球体生长和健康以及随时间推移的药物疗效的结果。总的来说,这项技术可能成为个性化医疗和未来药物开发的有用工具,有望降低医疗成本和缩短治疗时间。