In silico prediction and biological assessment of novel angiogenesis modulators from traditional Chinese medicine

被引:2
|
作者
Zhu, Yingli [1 ,2 ,3 ]
Yang, Hongbin [2 ]
Han, Liwen [4 ,5 ]
Mervin, Lewis H. [2 ]
Hosseini-Gerami, Layla [2 ]
Li, Peihai [4 ]
Wright, Peter [2 ]
Trapotsi, Maria-Anna [2 ]
Liu, Kechun [4 ]
Fan, Tai-Ping [3 ]
Bender, Andreas [2 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Mat Med, Dept Clin Chinese Pharm, Beijing, Peoples R China
[2] Univ Cambridge, Ctr Mol Sci Informat, Dept Chem, Cambridge, Cambs, England
[3] Univ Cambridge, Dept Pharmacol, Cambridge, Cambs, England
[4] Qilu Univ Technol, Biol Inst, Shandong Acad Sci, Engn Res Ctr Zebrafish Models Human Dis & Drug Scr, Jinan, Peoples R China
[5] Shandong First Med Univ, Shandong Acad Med Sci, Sch Pharm & Pharmaceut Sci, Jinan, Peoples R China
关键词
TCM; angiogenesis; mode of action; machine learning; biological assessment; MIGRATION INHIBITORY FACTOR; ENDOTHELIAL-CELLS; PROMOTING ANGIOGENESIS; INFLAMMATORY RESPONSE; TARGET PREDICTION; GENE-EXPRESSION; GROWTH; RECEPTOR; CANCER; MECHANISM;
D O I
10.3389/fphar.2023.1116081
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Uncontrolled angiogenesis is a common denominator underlying many deadly and debilitating diseases such as myocardial infarction, chronic wounds, cancer, and age-related macular degeneration. As the current range of FDA-approved angiogenesis-based medicines are far from meeting clinical demands, the vast reserve of natural products from traditional Chinese medicine (TCM) offers an alternative source for developing pro-angiogenic or anti-angiogenic modulators. Here, we investigated 100 traditional Chinese medicine-derived individual metabolites which had reported gene expression in MCF7 cell lines in the Gene Expression Omnibus (GSE85871). We extracted literature angiogenic activities for 51 individual metabolites, and subsequently analysed their predicted targets and differentially expressed genes to understand their mechanisms of action. The angiogenesis phenotype was used to generate decision trees for rationalising the poly-pharmacology of known angiogenesis modulators such as ferulic acid and curculigoside and validated by an in vitro endothelial tube formation assay and a zebrafish model of angiogenesis. Moreover, using an in silico model we prospectively examined the angiogenesis-modulating activities of the remaining 49 individual metabolites. In vitro, tetrahydropalmatine and 1 beta-hydroxyalantolactone stimulated, while cinobufotalin and isoalantolactone inhibited endothelial tube formation. In vivo, ginsenosides Rb3 and Rc, 1 beta-hydroxyalantolactone and surprisingly cinobufotalin, restored angiogenesis against PTK787-induced impairment in zebrafish. In the absence of PTK787, deoxycholic acid and ursodeoxycholic acid did not affect angiogenesis. Despite some limitations, these results suggest further refinements of in silico prediction combined with biological assessment will be a valuable platform for accelerating the research and development of natural products from traditional Chinese medicine and understanding their mechanisms of action, and also for other traditional medicines for the prevention and treatment of angiogenic diseases.
引用
收藏
页数:20
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