Drug Details
General Information of the Drug (ID: DR6904) | ||||
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Name |
Canstatin
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Disease | Hepatocellular carcinoma [ICD-11: 2C12] | Investigative | [1] |
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally | ||||||
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α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug | ||||||
Arsenic trioxide | Realgar and orpiment | Click to Show/Hide the Molecular Data of This NP | ||||
Achieving Therapeutic Synergy | Click to Show/Hide | |||||
Representative Experiment Reporting the Effect of This Combination | [1] | |||||
Detail(s) |
Combination Info
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Molecule(s)
Regulation |
Up-regulation | Expression | CASP3 | Molecule Info |
Pathway MAP
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Down-regulation | Expression | MMP-2 | Molecule Info |
Pathway MAP
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Down-regulation | Expression | PCNA | Molecule Info |
Pathway MAP
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In-vitro Model | Hep-G2 | CVCL_0027 | Hepatocellular carcinoma | Homo sapiens | ||
In-vivo Model | To establish nude mouse transplantation tumor model, 0.2 ml of HepG2 cells (1 * 107/ml) were injected subcutaneously in the right axilla of mice. | |||||
Experimental
Result(s) |
Combined canstatin and ATO significantly inhibited cell proliferation, migration and adhesion abilities, and promoted cell apoptosis, and inhibited tumor growth, thus suppressed the progression of HCC. |
Target and Pathway | ||||
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Target(s) | HIV Protease (HIV PR) | Molecule Info | [2] |


