Becattini Barbara, Kitada Shinichi, Leone Marilisa, Monosov Edward, Chandler Sharon, Zhai Dayong, Kipps Thomas J, Reed John C, Pellecchia Maurizio
The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Chem Biol. 2004 Mar;11(3):389-95. doi: 10.1016/j.chembiol.2004.02.020.
Antiapoptotic Bcl-2-family proteins Bcl-2 and Bcl-X(L) have been recently validated as drug discovery targets for cancer. Here, by using a combination of molecular modeling, NMR-based structural analysis, fluorescence polarization assays, and cell-based assays, we have designed and characterized a novel proapoptotic compound targeting these proteins. Our compound, Apogossypol, is capable of binding and inhibiting Bcl-2 and Bcl-X(L) with high affinity and induces apoptosis of tumor cell lines. Mechanistic studies on the action of our compound were also performed via confocal microscopy that provided real-time detection of the interaction with Bcl-X(L) in intact cells. Finally, preliminary data on cells freshly isolated from patients affected by chronic lymphocytic leukemia strongly suggest potential applications of Bcl-2 antagonists as chemosensitizers in cancer therapy.
抗凋亡Bcl-2家族蛋白Bcl-2和Bcl-X(L)最近已被确认为癌症药物研发的靶点。在此,我们通过分子建模、基于核磁共振的结构分析、荧光偏振分析和细胞分析相结合的方法,设计并表征了一种靶向这些蛋白的新型促凋亡化合物。我们的化合物脱镁叶绿酸能够以高亲和力结合并抑制Bcl-2和Bcl-X(L),并诱导肿瘤细胞系凋亡。还通过共聚焦显微镜对我们化合物的作用机制进行了研究,该显微镜可实时检测其在完整细胞中与Bcl-X(L)的相互作用。最后,从慢性淋巴细胞白血病患者新鲜分离的细胞的初步数据强烈表明,Bcl-2拮抗剂作为癌症治疗中的化学增敏剂具有潜在应用价值。