Roberge M, Berlinck R G, Xu L, Anderson H J, Lim L Y, Curman D, Stringer C M, Friend S H, Davies P, Vincent I, Haggarty S J, Kelly M T, Britton R, Piers E, Andersen R J
Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada.
Cancer Res. 1998 Dec 15;58(24):5701-6.
Treatment of cancer cells lacking p53 function with G2 checkpoint inhibitors sensitizes them to the toxic effects of DNA damage and has been proposed as a strategy for cancer therapy. However, few inhibitors are known, and they have been found serendipitously. We report the development of a G2 checkpoint inhibition assay that is suitable for high-throughput screening and its application to a screen of 1300 natural extracts. We present the isolation of a new G2 checkpoint inhibitor, the structurally novel compound isogranulatimide. In combination with gamma-irradiation, isogranulatimide selectively kills MCF-7 cells lacking p53 function.
用G2检查点抑制剂治疗缺乏p53功能的癌细胞可使其对DNA损伤的毒性作用敏感,并已被提出作为一种癌症治疗策略。然而,已知的抑制剂很少,且都是偶然发现的。我们报告了一种适用于高通量筛选的G2检查点抑制测定法的开发及其在1300种天然提取物筛选中的应用。我们展示了一种新的G2检查点抑制剂——结构新颖的化合物异颗粒酰胺的分离。与γ射线照射联合使用时,异颗粒酰胺可选择性杀死缺乏p53功能的MCF-7细胞。