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高剂量药物热图分析在多球体脑正常细胞和 GBM 患者来源细胞中的药物安全性和疗效。

High-dose drug heat map analysis for drug safety and efficacy in multi-spheroid brain normal cells and GBM patient-derived cells.

机构信息

Department of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.

Central R & D Center, Medical & Bio Device (MBD) Co., Ltd, Suwon, Republic of Korea.

出版信息

PLoS One. 2021 Dec 2;16(12):e0251998. doi: 10.1371/journal.pone.0251998. eCollection 2021.

Abstract

To test the safety and efficacy of drugs via a high does drug heat map, a multi-spheroids array chip was developed by adopting a micropillar and microwell structure. In the chip, patient-derived cells were encapsulated in alginate and grown to maturity for more than 7 days to form cancer multi-spheroids. Multi-spheroids grown in conventional well plates require many cells and are easily damaged as a result of multiple pipetting during maintenance culture or experimental procedures. To address these issues, we applied a micropillar and microwell structure to the multi-spheroids array. Patient-derived cells from patients with Glioblastoma (GBM), the most common and lethal form of central nervous system cancer, were used to validate the array chip performance. After forming multi-spheroids with a diameter greater than 100μm in a 12×36 pillar array chip (25mm × 75mm), we tested 70 drug compounds (6 replicates) using a high-dose to determine safety and efficacy for drug candidates. Comparing the drug response of multi-spheroids derived from normal cells and cancer cells, we found that four compounds (Dacomitinib, Cediranib, LY2835219, BGJ398) did not show toxicity to astrocyte cell and were efficacious to patient-derived GBM cells.

摘要

为了通过高剂量药物热图测试药物的安全性和有效性,我们采用微柱和微孔结构开发了一种多球体阵列芯片。在该芯片中,患者来源的细胞被包裹在藻酸盐中,并生长成熟超过 7 天,以形成癌症多球体。在常规培养板中生长的多球体需要大量细胞,并且在维持培养或实验过程中多次移液操作容易受到损伤。为了解决这些问题,我们将微柱和微孔结构应用于多球体阵列。使用来自胶质母细胞瘤(GBM)患者的患者来源细胞,这是中枢神经系统癌症中最常见和最致命的形式,来验证该芯片的性能。在 12×36 柱阵列芯片(25mm×75mm)中形成直径大于 100μm 的多球体后,我们使用高剂量测试了 70 种药物化合物(6 个重复),以确定候选药物的安全性和有效性。将正常细胞和癌细胞来源的多球体的药物反应进行比较,我们发现四种化合物(达可替尼、西地尼布、LY2835219、BGJ398)对星形胶质细胞没有毒性,并且对患者来源的 GBM 细胞有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/539f/8638871/3680b31b4efb/pone.0251998.g001.jpg

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