癌症治疗
计算机科学
癌症
药物发现
癌症治疗
药品
药物开发
计算生物学
生物信息学
医学
生物
药理学
内科学
作者
Yung-Hao Wong,Chia-Chiun Chiu,Chih‐Lung Lin,Ting-Shou Chen,Bo-Ren Jheng,Yu‐Ching Lee,Jeremy J.W. Chen,Bor‐Sen Chen
出处
期刊:Current Pharmaceutical Biotechnology
[Bentham Science]
日期:2016-11-03
卷期号:17 (14): 1246-1267
被引量:8
标识
DOI:10.2174/1389201017666161019160606
摘要
In recent years, many systems biology approaches have been used with various cancers. The materials described here can be used to build bases to discover novel cancer therapy targets in connection with computer-aided drug design (CADD). A deeper understanding of the mechanisms of cancer will provide more choices and correct strategies in the development of multiple target drug therapies, which is quite different from the traditional cancer single target therapy. Targeted therapy is one of the most powerful strategies against cancer and can also be applied to other diseases. Due to the large amount of progress in computer hardware and the theories of computational chemistry and physics, CADD has been the main strategy for developing novel drugs for cancer therapy. In contrast to traditional single target therapies, in this review we will emphasize the future direction of the field, i.e., multiple target therapies. Structure-based and ligand-based drug designs are the two main topics of CADD. The former needs both 3D protein structures and ligand structures, while the latter only needs ligand structures. Ordinarily it is estimated to take more than 14 years and 800 million dollars to develop a new drug. Many new CADD software programs and techniques have been developed in recent decades. We conclude with an example where we combined and applied systems biology and CADD to the core networks of four cancers and successfully developed a novel cocktail for drug therapy that treats multiple targets. Keywords: Carcinogenesis, network markers, carcinogenesis relevance value, protein-protein interactions, computer-aided drug design, multiple target cocktail.
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