拓扑替康
小RNA
癌症研究
化学
克隆形成试验
Oncomir公司
细胞培养
小分子
细胞毒性
细胞凋亡
细胞
生物
生物化学
化疗
体外
基因
遗传学
作者
Yuta Naro,Nicholas Ankenbruck,Méryl Thomas,Yaniv Tivon,Colleen M. Connelly,Laura Gardner,Alexander Deiters
标识
DOI:10.1021/acs.jmedchem.7b01891
摘要
Chemical probes of microRNA (miRNA) function are potential tools for understanding miRNA biology that also provide new approaches for discovering therapeutics for miRNA-associated diseases. MicroRNA-21 (miR-21) is an oncogenic miRNA that is overexpressed in most cancers and has been strongly associated with driving chemoresistance in cancers such as renal cell carcinoma (RCC). Using a cell-based luciferase reporter assay to screen small molecules, we identified a novel inhibitor of miR-21 function. Following structure-activity relationship studies, an optimized lead compound demonstrated cytotoxicity in several cancer cell lines. In a chemoresistant-RCC cell line, inhibition of miR-21 via small molecule treatment rescued the expression of tumor-suppressor proteins and sensitized cells to topotecan-induced apoptosis. This resulted in a >10-fold improvement in topotecan activity in cell viability and clonogenic assays. Overall, this work reports a novel small molecule inhibitor for perturbing miR-21 function and demonstrates an approach to enhancing the potency of chemotherapeutics specifically for cancers derived from oncomir addiction.
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