Department of Chemistry and Biochemistry and ‡Harper Cancer Research Institute, University of Notre Dame , Notre Dame, Indiana 46556, United States.
Anal Chem. 2018 Jan 16;90(2):1423-1430. doi: 10.1021/acs.analchem.7b04969. Epub 2017 Dec 21.
For a patient with metastatic colorectal cancer there are limited clinical options aside from chemotherapy. Unfortunately, the development of new chemotherapeutics is a long and costly process. New methods are needed to identify promising drug candidates earlier in the drug development process. Most chemotherapies are administered to patients in combinations. Here, an in vitro platform is used to assess the penetration and metabolism of combination chemotherapies in three-dimensional colon cancer cell cultures, or spheroids. Colon carcinoma HCT 116 cells were cultured and grown into three-dimensional cell culture spheroids. These spheroids were then dosed with a common combination chemotherapy, FOLFIRI (folinic acid, 5-fluorouracil, and irinotecan) in a 3D printed fluidic device. This fluidic device allows for the dynamic treatment of spheroids across a semipermeable membrane. Following dosing, the spheroids were harvested for quantitative proteomic profiling to examine the effects of the combination chemotherapy on the colon cancer cells. Spheroids were also imaged to assess the spatial distribution of administered chemotherapeutics and metabolites with MALDI-imaging mass spectrometry. Following treatment, we observed penetration of folinic acid to the core of spheroids and metabolism of the drug in the outer proliferating region of the spheroid. Proteomic changes identified included an enrichment of several cancer-associated pathways. This innovative dosing device, along with the proteomic evaluation with iTRAQ-MS/MS, provides a robust platform that could have a transformative impact on the preclinical evaluation of drug candidates. This system is a high-throughput and cost-effective approach to examine novel drugs and drug combinations prior to animal testing.
对于转移性结直肠癌患者,除化疗外,临床选择有限。不幸的是,新的化疗药物的开发是一个漫长而昂贵的过程。需要新的方法来更早地在药物开发过程中识别有前途的药物候选物。大多数化疗药物都是联合给药给患者。在这里,使用体外平台来评估组合化疗药物在三维结肠癌细胞培养物(或球体)中的渗透和代谢。结肠癌细胞系 HCT 116 细胞被培养并生长成三维细胞培养球体。然后,这些球体用常见的组合化疗药物 FOLFIRI(亚叶酸、5-氟尿嘧啶和伊立替康)在 3D 打印的流体设备中进行给药。这种流体设备允许在半渗透膜上对球体进行动态治疗。给药后,从球体中收获进行定量蛋白质组学分析,以检查组合化疗对结肠癌细胞的影响。还对球体进行成像,以使用 MALDI-成像质谱法评估给药的化疗药物和代谢物的空间分布。治疗后,我们观察到亚叶酸渗透到球体的核心,以及药物在球体的外增殖区域的代谢。鉴定的蛋白质组学变化包括几种癌症相关途径的富集。这种创新的给药装置以及 iTRAQ-MS/MS 的蛋白质组学评估,提供了一个强大的平台,可能对候选药物的临床前评估产生变革性影响。该系统是一种高通量且具有成本效益的方法,可在动物试验之前检查新药物和药物组合。