Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, Pennsylvania 19102, USA.
J Med Chem. 2012 Apr 12;55(7):3011-20. doi: 10.1021/jm201173g. Epub 2012 Mar 19.
The homologous recombination (HR) pathway plays a crucial role in the repair of DNA double-strand breaks (DSBs) and interstrand cross-links (ICLs). RAD51, a key protein of HR, possesses a unique activity: DNA strand exchange between homologous DNA sequences. Recently, using a high-throughput screening (HTS), we identified compound 1 (B02), which specifically inhibits the DNA strand exchange activity of human RAD51. Here, we analyzed the mechanism of inhibition and found that 1 disrupts RAD51 binding to DNA. We then examined the effect of 1 on HR and DNA repair in the cell. The results show that 1 inhibits HR and increases cell sensitivity to DNA damage. We propose to use 1 for analysis of cellular functions of RAD51. Because DSB- and ICL-inducing agents are commonly used in anticancer therapy, specific inhibitors of RAD51 may also help to increase killing of cancer cells.
同源重组 (HR) 途径在修复 DNA 双链断裂 (DSB) 和链间交联 (ICL) 中起着至关重要的作用。RAD51 是 HR 的关键蛋白,具有独特的活性:同源 DNA 序列之间的 DNA 链交换。最近,我们使用高通量筛选 (HTS) 发现了化合物 1 (B02),它特异性抑制人 RAD51 的 DNA 链交换活性。在这里,我们分析了抑制机制,发现 1 破坏 RAD51 与 DNA 的结合。然后,我们研究了 1 对细胞中 HR 和 DNA 修复的影响。结果表明,1 抑制 HR 并增加细胞对 DNA 损伤的敏感性。我们建议使用 1 来分析 RAD51 的细胞功能。因为 DSB 和 ICL 诱导剂常用于癌症治疗,RAD51 的特异性抑制剂也可能有助于增加癌细胞的杀伤。