Blumberg P M, Kedei N, Lewin N E, Yang D, Czifra G, Pu Y, Peach M L, Marquez V E
Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Center, Bethesda, MD 20892, USA.
Curr Drug Targets. 2008 Aug;9(8):641-52. doi: 10.2174/138945008785132376.
The diacylglycerol-responsive C1 domains of protein kinase C and of the related classes of signaling proteins represent highly attractive targets for drug development. The signaling functions that are regulated by C1 domains are central to cellular control, thereby impacting many pathological conditions. Our understanding of the diacylglycerol signaling pathways provides great confidence in the utility of intervention in these pathways for treatment of cancer and other conditions. Multiple compounds directed at these signaling proteins, including compounds directed at the C1 domains, are currently in clinical trials, providing strong validation for these targets. Extensive understanding of the structure and function of C1 domains, coupled with detailed insights into the molecular details of ligand - C1 domain interactions, provides a solid basis for rational and semi-rational drug design. Finally, the complexity of the factors contributing to ligand - C1 domain interactions affords abundant opportunities for manipulation of selectivity; indeed, substantially selective compounds have already been identified.
蛋白激酶C以及相关信号蛋白类别的二酰基甘油反应性C1结构域是药物开发极具吸引力的靶点。由C1结构域调节的信号功能是细胞控制的核心,从而影响许多病理状况。我们对二酰基甘油信号通路的理解为干预这些通路以治疗癌症和其他疾病的效用提供了极大的信心。目前,多种针对这些信号蛋白的化合物,包括针对C1结构域的化合物,正处于临床试验阶段,这为这些靶点提供了有力的验证。对C1结构域的结构和功能有广泛的了解,再加上对配体与C1结构域相互作用分子细节的深入洞察,为合理和半合理的药物设计提供了坚实的基础。最后,导致配体与C1结构域相互作用的因素的复杂性为选择性操纵提供了丰富的机会;事实上,已经鉴定出了具有显著选择性的化合物。