Central R&D Institute, Samsung Electro-Mechanics Co (SEMCO), Suwon, Republic of Korea.
Arch Toxicol. 2014 Feb;88(2):283-90. doi: 10.1007/s00204-013-1102-9. Epub 2013 Jul 28.
The DataChip is a universal platform for three-dimensional (3D) cell cultures on a micropillar chip, which can be applicable to a variety of human cells to simulate organ-specific toxicity. In addition, the MetaChip is developed for various combinations of drug metabolizing enzymes that can be spotted into the microwell chip and incubated with 3D human cells to simulate systematic compound metabolism in the human liver on a microscale format. Ajoenes have been known for various therapeutics activities, including anticancer effects, but there was limited information available in regard to their metabolism and cytotoxicity. In the present work, the metabolism-mediated toxicity of ajoenes was evaluated on a DataChip/MetaChip platform. In detail, we tested cytotoxicity of E- and Z-ajoene on 3D cultured Hep3B human hepatoma cells coupled with mixtures of drug metabolizing enzymes. Metabolic profiles of ajoenes were assessed with 23 representative drug metabolizing enzymes on the MetaChip. As a result, cytotoxicity of E-ajoene was significantly augmented in the presence of cytochrome P450 (CYP) isoforms, such as CYP2E1 and CYP3A5. Both E- and Z-ajoene were drastically detoxified in the presence of Phase II enzymes, including major UGTs, SULTs, NATs, and GSTs. Interestingly, All Mix, an artificial human liver microsome containing representative P450 mixture and phase II enzyme mixture, attenuated P450-induced cytotoxicity of ajoenes. Conclusively, we were able to confirm the metabolism-medicated toxicity of ajoenes on the chip.
DataChip 是一种用于微柱芯片上三维(3D)细胞培养的通用平台,可适用于各种人类细胞,以模拟器官特异性毒性。此外,MetaChip 是为各种药物代谢酶的组合开发的,可以点入微孔芯片中,并与 3D 人类细胞孵育,以在微尺度格式模拟人类肝脏中的系统化合物代谢。阿霍烯具有各种治疗活性,包括抗癌作用,但关于其代谢和细胞毒性的信息有限。在本工作中,在 DataChip/MetaChip 平台上评估了阿霍烯的代谢介导的毒性。具体而言,我们测试了 E-和 Z-阿霍烯对 3D 培养的 Hep3B 人肝癌细胞的细胞毒性,同时与药物代谢酶的混合物一起测试。用 MetaChip 上的 23 种代表性药物代谢酶评估了阿霍烯的代谢谱。结果表明,在细胞色素 P450(CYP)同工酶(如 CYP2E1 和 CYP3A5)存在的情况下,E-阿霍烯的细胞毒性显著增强。E-和 Z-阿霍烯在 II 相酶(包括主要的 UGTs、SULTs、NATs 和 GSTs)存在的情况下被大大解毒。有趣的是,All Mix,一种含有代表性 P450 混合物和 II 相酶混合物的人工人肝微粒体,减弱了 P450 诱导的阿霍烯细胞毒性。总之,我们能够在芯片上确认阿霍烯的代谢介导的毒性。