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Network pharmacology-based study of anti-hepatoma effects and mechanisms of matrine
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Ke-xin WANG1, 2, Li GAO1, Yu-zhi ZHOU1, *, Jian-qin ZHANG1, Xue-mei QIN1, Guan-hua DU3, *
Acta Pharmaceutica Sinica | 2017, 52(6) : 888 - 896
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Acta Pharmaceutica Sinica | 2017, 52(6): 888-896
ORIGINAL ARTICLES·Pharmacology
Network pharmacology-based study of anti-hepatoma effects and mechanisms of matrine
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Ke-xin WANG1, 2, Li GAO1, Yu-zhi ZHOU1, *, Jian-qin ZHANG1, Xue-mei QIN1, Guan-hua DU3, *
Affiliations
  • 1. Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China
  • 2. College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China
  • 3. Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Published: 2017-06-12 doi: 10.16438/j.0513-4870.2017-0075
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Although multiple studies have shown that matrine can inhibit the proliferation of hepatoma cells, its mechanism of action has not been systematically investigated. In this study, the effects of matrine on the proliferation and migration of human hepatoma SMMC-7721 cells were investigated. Based on this result, anti-hepatoma target-functionally related protein interaction network of matrine was constructed, and topological analysis and clustering analysis were performed to predict the crucial targets of matrine for the anti-hepatoma effects. Pathway enrichment analysis was performed on the validated targets to predict the crucial pathways of matrine. Parts of the crucial proteins were examined by Western blot. Cellular experiments showed that matrine at concentrations of 1, 2 and 4 mg·mL-1 significantly inhibited the proliferation of SMMC-7721 cells, and matrine at concentrations of 0.5, 1 and 2 mg·mL-1 significantly inhibited the migration of SMMC-7721 cells. The results of network pharmacology suggest that matrine exerts its anti-hepatoma effects through acting on the key validated targets of heparanase (HPSE), caspase 3 (CASP3), Myc proto-oncogene protein (MYC), matrix metalloproteinases 2 (MMP2) and predicted targets of carbonic anhydrase 1 (CA1), lithostathine 1 alpha precursor (REG1A), carboxylesterases 1 (CES1) and acetaldehyde dehydrogenase 2 (ALDH2), and invasion and migration associated pathways. Western blot results suggest that matrine can down-regulate the expression of MMP2 and up-regulate the expression of CASP3. In this paper, we applied network pharmacology to explain the targets and pathways of matrine against hepatoma. The results provide a scientific basis for elucidation of the mechanisms of matrine against hepatoma.

network pharmacology  /  matrine  /  hepatoma  /  mechanism
Ke-xin WANG, Li GAO, Yu-zhi ZHOU, Jian-qin ZHANG, Xue-mei QIN, Guan-hua DU. Network pharmacology-based study of anti-hepatoma effects and mechanisms of matrine[J]. Acta Pharmaceutica Sinica, 2017 , 52 (6) : 888 -896 . DOI: 10.16438/j.0513-4870.2017-0075
Year 2017 volume 52 Issue 6
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Article Info
doi: 10.16438/j.0513-4870.2017-0075
  • Receive Date:2017-01-17
  • Online Date:2026-01-14
  • Published:2017-06-12
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History
  • Received:2017-01-17
  • Revised:2017-03-03
Funding
Affiliations
    1. Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China
    2. College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China
    3. Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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