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结直肠癌细胞球体的高通量筛选。

High-throughput screening in colorectal cancer tissue-originated spheroids.

机构信息

Department of Clinical Bio-resource Research and Development, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Biochemistry, Osaka International Cancer Institute, Osaka, Japan.

出版信息

Cancer Sci. 2019 Jan;110(1):345-355. doi: 10.1111/cas.13843. Epub 2018 Nov 20.

Abstract

Patient-derived cancer organoid culture is an important live material that reflects clinical heterogeneity. However, the limited amount of organoids available for each case as well as the considerable amount of time and cost to expand in vitro makes it impractical to perform high-throughput drug screening using organoid cultures from multiple patients. Here, we report an advanced system for the high-throughput screening of 2427 drugs using the cancer tissue-originated spheroid (CTOS) method. In this system, we apply the CTOS method in an ex vivo platform from xenograft tumors, using machines to handle CTOS and reagents, and testing a CTOS reference panel of multiple CTOS lines for the hit drugs. CTOS passages in xenograft tumors resulted in minimal changes of morphological and genomic status, and xenograft tumor generation efficiently expanded the number of CTOS to evaluate multiple drugs. Our panel of colorectal cancer CTOS lines exhibited diverse sensitivities to the hit compounds, demonstrating the usefulness of this system for investigating highly heterogeneous disease.

摘要

患者来源的肿瘤类器官培养物是一种重要的活体材料,反映了临床异质性。然而,每个病例可获得的类器官数量有限,并且体外扩增需要大量的时间和成本,这使得使用来自多个患者的类器官培养物进行高通量药物筛选变得不切实际。在这里,我们报告了一种使用肿瘤组织来源的球体(CTOS)方法进行 2427 种药物高通量筛选的先进系统。在该系统中,我们将 CTOS 方法应用于异种移植瘤的体外平台,使用机器处理 CTOS 和试剂,并测试多种 CTOS 系的 CTOS 参考面板以确定候选药物。在异种移植瘤中进行 CTOS 传代会导致形态和基因组状态的微小变化,并且异种移植瘤的生成有效地扩大了 CTOS 的数量以评估多种药物。我们的结直肠癌 CTOS 系面板对候选化合物表现出不同的敏感性,证明了该系统在研究高度异质性疾病方面的有用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c664/6317944/e4ceedc7d08d/CAS-110-345-g001.jpg

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