The forecast of anticancer targets of cryptotanshinone based on reverse pharmacophore-based screening technology

被引:22
作者
Yuan Dong-Ping [1 ]
Long Jun [1 ]
Lu Yin [2 ]
Lin Jie [3 ]
Tong Li [4 ]
机构
[1] Nanjing Univ Chinese Med, Coll Pharm, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Jiangsu Key Lab Pharmacol & Safety Evaluat Chines, Nanjing 210029, Jiangsu, Peoples R China
[3] Yunnan Univ, Sch Life Sci, Kunming 650091, Peoples R China
[4] Qinghai Univ, Tradit Chinese & Tibetan Med Res Ctr, Coll Med, Xining 810001, Peoples R China
基金
中国国家自然科学基金;
关键词
Cryptotanshinone; Pharmacophore; Reverse screening technology; Anticancer; Human hepatoma cells; Forecast of target; DISCOVERY;
D O I
10.1016/S1875-5364(14)60069-8
中图分类号
R [医药、卫生];
学科分类号
100218 [急诊医学];
摘要
Anticancer targets of cryptotanshinone were evaluated and rapidly forecasted with PharmMapper, a reverse pharmacophore-based screening platform, as well as chug target databases, including PDTD, DrugBank and TTD. The pathway analyses for the collection of anticancer targets screened were carried out based on the KEGG pathway database, followed by the forecast of potential pharmacological activities and pathways of the effects of cryptotanshinone, and verification of some of the targets screened using whole cell tests. The results showed that a total of eight targets with anticancer potential were screened, including MAP2K1, RAR alpha, RXR alpha, PDK1, CBK1, AR, Ang-1 R, and Kif11. These targets are mainly related to four aspects of the cancer growth: the cell cycle, angiogenesis, apoptosis, and androgen receptor. The cell tests showed that cryptotanshinone can inhibit the viability of human hepatoma cells SMMC-7721, which is related to the reduction of expression of MAP2K1 mRNA. This method provides a strong clue for the study of the anticancer effects and mechanisms of action of cryptotanshinone in the future.
引用
收藏
页码:443 / 448
页数:6
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