Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, 18 Baixincang, Dongzhimennei, Beijing 100700, China.
Expert Opin Drug Discov. 2012 Aug;7(8):667-77. doi: 10.1517/17460441.2012.692673. Epub 2012 Jun 10.
Effective regulation of abnormal targets of disease requires the alteration of either the topological structure or dynamic characteristics of modules in a given target network. In order to disturb the complex direct and indirect target hubs, new approaches in adaptive pharmacology should be developed to regulate target loops using module-based designs.
This review discusses the formation in disease-associated structural networks with multiple drug targets and the optimization of a multi-objective system of modules.
On the basis of these concepts, modular pharmacology (MP) has emerged as a method that can balance multiple outcomes by regulating the response of property modules on the basis of the benefits and risks of diversified modules and drugs, thereby allowing novel approaches for drug discovery. Further research of pharmacological mechanisms underlying diversity interactions between multiple modules is necessary for a better understanding of the basic therapeutic processes.
有效调节疾病的异常靶点需要改变给定靶点网络中模块的拓扑结构或动态特性。为了扰乱复杂的直接和间接靶点枢纽,应开发适应性药理学中的新方法,使用基于模块的设计来调节靶点环。
本文讨论了与多种药物靶点相关的疾病相关结构网络的形成,以及模块的多目标系统的优化。
基于这些概念,模块化药理学(MP)已经成为一种方法,它可以通过调节多样化模块和药物的属性模块的响应来平衡多种结果,从而为药物发现提供新的方法。进一步研究多个模块之间多样性相互作用的药理学机制,对于更好地理解基本治疗过程是必要的。