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Drug Design of Cyclin-Dependent Kinase 2 Inhibitor for Melanoma from Traditional Chinese Medicine
被引:11
作者:
Tang, Hsin-Chieh
[1
]
Chen, Calvin Yu-Chian
[1
,2
,3
,4
]
机构:
[1] Asia Univ, Dept Biomed Informat, Taichung 41354, Taiwan
[2] China Med Univ, Dept Med, Taichung 40402, Taiwan
[3] China Med Univ, Res Ctr Chinese Med & Acupuncture, Taichung 40402, Taiwan
[4] China Med Univ Hosp, Dept Med Res, Human Genet Ctr, Taichung 40447, Taiwan
关键词:
CELL-CYCLE;
PROTEIN;
CANCER;
RESISTANCE;
EXPRESSION;
POTENT;
CDK2;
GENE;
P21;
SIMULATION;
D O I:
10.1155/2014/798742
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
One has found an important cell cycle controller. This guard can decide the cell cycle toward proliferation or quiescence. Cyclin-dependent kinase 2 (CDK2) is a unique target among the CDK family in melanoma therapy. We attempted to find out TCM compounds from TCM Database@Taiwan that have the ability to inhibit the activity of CDK2 by systems biology. We selected Tetrahydropalmatine, Reserpiline, and (+)-Corydaline as the candidates by docking and screening results for further survey. We utilized support vectormachine (SVM), multiple linear regression (MLR) models and Bayesian network for validation of predicted activity. By overall analysis of docking results, predicted activity, and molecular dynamics (MD) simulation, we could conclude that Tetrahydropalmatine, Reserpiline, and (+)-Corydaline had better binding affinity than the control. All of them had the ability to inhibit the activity of CDK2 and might have the opportunity to be applied in melanoma therapy.
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页数:17
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