Pinho Diana, Santos Denis, Vila Ana, Carvalho Sandra
International Iberian Nanotechnology Laboratory, Department of Nanoelectronics Engineering, 4715-330 Braga, Portugal.
International Iberian Nanotechnology Laboratory, IP Exploitation and Knowledge Transfer, 4715-330 Braga, Portugal.
Micromachines (Basel). 2021 Apr 28;12(5):497. doi: 10.3390/mi12050497.
Colorectal cancer is the second leading cause of cancer death worldwide. Significant advances in the molecular mechanisms underlying colorectal cancer have been made; however, the clinical approval of new drugs faces many challenges. Drug discovery is a lengthy process causing a rapid increase in global health care costs. Patient-derived tumour organoids are considered preclinical models with the potential for preclinical drug screening, prediction of patient outcomes, and guiding optimized therapy strategies at an individual level. Combining microfluidic technology with 3D tumour organoid models to recapitulate tumour organization and in vivo functions led to the development of an appropriate preclinical tumour model, organoid-on-a-chip, paving the way for personalized cancer medicine. Herein, a low-cost microfluidic device suitable for culturing and expanding organoids, OrganoidChip, was developed. Patient-derived colorectal cancer organoids were cultured within OrganoidChip, and their viability and proliferative activity increased significantly. No significant differences were verified in the organoids' response to 5-fluorouracil (5-FU) treatment on-chip and on-plate. However, the culture within the OrganoidChip led to a significant increase in colorectal cancer organoid-forming efficiency and overall size compared with conventional culture on a 24-well plate. Interestingly, early-stage and late-stage organoids were predominantly observed on-plate and within the OrganoidChip, respectively. The OrganoidChip thus has the potential to generate in vivo-like organotypic structures for disease modelling and drug screening applications.
结直肠癌是全球癌症死亡的第二大主要原因。在结直肠癌潜在的分子机制方面已取得重大进展;然而,新药的临床批准面临诸多挑战。药物研发是一个漫长的过程,导致全球医疗保健成本迅速增加。患者来源的肿瘤类器官被视为具有临床前药物筛选、预测患者预后以及在个体水平指导优化治疗策略潜力的临床前模型。将微流控技术与3D肿瘤类器官模型相结合以重现肿瘤组织和体内功能,促成了一种合适的临床前肿瘤模型——芯片上类器官的开发,为个性化癌症医学铺平了道路。在此,开发了一种适用于培养和扩增类器官的低成本微流控装置——类器官芯片。在类器官芯片内培养患者来源的结直肠癌类器官,其活力和增殖活性显著增加。芯片上和培养皿上的类器官对5-氟尿嘧啶(5-FU)治疗的反应未证实有显著差异。然而,与在24孔板上的传统培养相比,在类器官芯片内培养导致结直肠癌类器官形成效率和总体尺寸显著增加。有趣的是,在培养皿上和类器官芯片内分别主要观察到早期和晚期类器官。因此,类器官芯片有潜力生成用于疾病建模和药物筛选应用的体内样器官型结构。