A Potential Target of Tanshinone IIA for Acute Promyelocytic Leukemia Revealed by Inverse Docking and Drug Repurposing

被引:29
作者
Chen, Shao-Jun [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Basic Med Sci, Div Neurobiol & Physiol, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Pharmaceut Coll, Dept Tradit Chinese Med, Ningbo, Zhejiang, Peoples R China
关键词
Acute promyelocytic leukemia; chemical-protein interactome; drug repurposing; inverse docking; IN-VIVO; CELLS; IDENTIFICATION; DISCOVERY; APOPTOSIS; RAR;
D O I
10.7314/APJCP.2014.15.10.4301
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Tanshinone IIA is a pharmacologically active ingredient extracted from Danshen, a Chinese traditional medicine. Its molecular mechanisms are still unclear. The present study utilized computational approaches to uncover the potential targets of this compound. In this research, PharmMapper server was used as the inverse docking tool andnd the results were verified by Autodock vina in PyRx 0.8, and by DRAR-CPI, a server for drug repositioning via the chemical-protein interactome. Results showed that the retinoic acid receptor alpha (RAR alpha), a target protein in acute promyelocytic leukemia (APL), was in the top rank, with a pharmacophore model matching well the molecular features of Tanshinone IIA. Moreover, molecular docking and drug repurposing results showed that the complex was also matched in terms of structure and chemical-protein interactions. These results indicated that RARa may be a potential target of Tanshinone IIA for APL. The study can provide useful information for further biological and biochemical research on natural compounds.
引用
收藏
页码:4301 / 4305
页数:5
相关论文
共 33 条
[1]
Achenbach J, 2011, FUTURE MED CHEM, V3, P961, DOI [10.4155/FMC.11.62, 10.4155/fmc.11.62]
[2]
Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations [J].
Akagi, Tadayuki ;
Shih, Lee-Yung ;
Kato, Motohiro ;
Kawamata, Norihiko ;
Yamamoto, Go ;
Sanada, Masashi ;
Okamoto, Ryoko ;
Miller, Carl W. ;
Liang, Der-Cherng ;
Ogawa, Seishi ;
Koeffler, H. Phillip .
BLOOD, 2009, 113 (08) :1741-1748
[3]
[Anonymous], P NATL ACAD SCI US, V105, P4826
[4]
Identification of Proapoptopic, Anti-Inflammatory, Anti-Proliferative, Anti-Invasive and Anti-Angiogenic Targets of Essential Oils in Cardamom by Dual Reverse Virtual Screening and Binding Pose Analysis [J].
Bhattacharjee, Biplab ;
Chatterjee, Jhinuk .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2013, 14 (06) :3735-3742
[5]
Comparative Reverse Screening Approach to Identify Potential Anti-neoplastic Targets of Saffron Functional Components and Binding Mode [J].
Bhattacharjee, Biplab ;
Vijayasarathy, Sandhya ;
Karunakar, Prashantha ;
Chatterjee, Jhinuk .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (11) :5605-5611
[6]
Crystal structure of a heterodimeric complex of RAR and RXR ligand-binding domains [J].
Bourguet, W ;
Vivat, V ;
Wurtz, JM ;
Chambon, P ;
Gronemeyer, H ;
Moras, D .
MOLECULAR CELL, 2000, 5 (02) :289-298
[7]
Identification of a Potential Anticancer Target of Danshensu by Inverse Docking [J].
Chen, Shao-Jun ;
Ren, Ji-Long .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2014, 15 (01) :111-116
[8]
Chen YZ, 2001, PROTEINS, V43, P217, DOI 10.1002/1097-0134(20010501)43:2<217::AID-PROT1032>3.0.CO
[9]
2-G
[10]
Acute promyelocytic leukaemia: novel insights into the mechanisms of cure [J].
de The, Hugues ;
Chen, Zhu .
NATURE REVIEWS CANCER, 2010, 10 (11) :775-783