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一种用于高通量筛选抑制 survivin 的癌症药物的荧光 3D 细胞培养测定法。

A fluorescent 3D cell culture assay for high throughput screening of cancer drugs down-regulating survivin.

机构信息

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, 151 West Woodruff Ave., Columbus, Ohio, 43210, USA.

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, 151 West Woodruff Ave., Columbus, Ohio, 43210, USA.

出版信息

J Biotechnol. 2019 Jan 10;289:80-87. doi: 10.1016/j.jbiotec.2018.11.018. Epub 2018 Nov 22.

Abstract

Survivin, a member of inhibitor of apoptosis family, is currently undergoing intensive investigations as a promising cancer marker due to its overexpression in multiple tumor tissues and close relationship with chemotherapy resistance. In this study, a novel 3D survivin promoter assay was developed, using enhanced green fluorescent protein (EGFP) as the reporter to assess survivin promoter activity for cancer drug screening. Breast cancer MCF-7 cells were engineered to express EGFP controlled by a human survivin promoter and a CMV promoter, respectively. These cells were cultured in three-dimensional (3D) polymer-based scaffolds on a 40-microbioreactor platform (40-MBR) with real-time monitoring of EGFP signals. The EGFP production driven by the survivin promoter was strongly correlated with survivin transcriptional level in MCF-7 cells treated with YM155, a small-molecule survivin promoter suppressant. Moreover, the potential inhibition effects of doxorubicin and cisplatin on survivin and their cytotoxicity were also evaluated in this system. This study demonstrated the potential application of the novel 3D survivin promoter-EGFP reporter assay for high-throughput screening of chemicals down-regulating survivin as a molecular target for cancer therapy.

摘要

Survivin,凋亡抑制因子家族的一员,由于其在多种肿瘤组织中的过度表达及其与化疗耐药性的密切关系,目前正作为一种很有前途的癌症标志物进行深入研究。在这项研究中,开发了一种新型的 3D survivin 启动子测定法,使用增强型绿色荧光蛋白(EGFP)作为报告基因,评估 survivin 启动子活性,用于癌症药物筛选。将乳腺癌 MCF-7 细胞工程改造为表达 EGFP,分别受人类 survivin 启动子和 CMV 启动子的控制。这些细胞在 40 微生物反应器平台(40-MBR)上的三维聚合物基质中培养,实时监测 EGFP 信号。在 YM155(一种小分子 survivin 启动子抑制剂)处理的 MCF-7 细胞中,由 survivin 启动子驱动的 EGFP 产生与 survivin 的转录水平密切相关。此外,还在该系统中评估了多柔比星和顺铂对 survivin 的潜在抑制作用及其细胞毒性。本研究表明,新型 3D survivin 启动子-EGFP 报告基因测定法可用于高通量筛选下调 survivin 的化学物质,作为癌症治疗的分子靶标。

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