摘要:膀胱癌三维高通量药物筛选

Sang-Cheol Lee, Young Saing Kim, I. Hwang, Su Jin Lee, S. Park
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引用次数: 0

摘要

膀胱癌发生的分子机制的最新进展为特异性靶向信号通路提供了前景,以实现更有效和合理的治疗。在一种新型的三维高通量药物筛选(3D HTS)平台上,鉴定了影响膀胱癌细胞的新型药物,在7种人类膀胱癌细胞系(UCUM3、T24、SW780、RT4、J82、5637和253J-BV)中筛选了24种分子靶向药物。24种靶向药物对膀胱细胞系的作用效果因其基因组改变而有显著差异。BEZ235 (mTOR和PI3K抑制剂)在除UMUC3外的大多数细胞系中均表现出抗肿瘤作用。另一种mTOR抑制剂AZD2014 (mTORC1和mTORC2的抑制剂)也具有IC50。引文格式:李尚哲,金英生,黄仁圭,李秀珍,朴世勋。膀胱癌三维高通量药物筛选[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志,2019;79(13增刊):第997期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 997: Three-dimensional high-throughput drug screening for bladder cancer
Recent progress in understanding the molecular mechanisms that underlie bladder cancer carcinogenesis offers the prospect of specifically targeting signaling pathways to achieve more effective and rational treatment. In a novel, 3-dimensional high-throughput drug screening (3D HTS) platform to identify novel agents affecting bladder cancer cells, 24 molecularly-targeted agents were screened in seven human bladder cancer cell lines (UCUM3, T24, SW780, RT4, J82, 5637 and 253J-BV). The efficacy of 24 targeted agents on the bladder cell lines varied dramatically on their genomic alterations. BEZ235 (mTOR and PI3K inhibitor) showed antitumor effect in most of cell lines except UMUC3. Another mTOR inhibitor, AZD2014 (inhibitors of mTORC1 and mTORC2) also had IC50 Note: This abstract was not presented at the meeting. Citation Format: Sang-Cheol Lee, Young Saing Kim, In Gyu Hwang, Su Jin Lee, Se Hoon Park. Three-dimensional high-throughput drug screening for bladder cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 997.
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