Pair Name | Lupeol, Enzalutamide | ||
Phytochemical Name | Lupeol (PubChem CID: 259846 ) | ||
Anticancer drug Name | Enzalutamide (PubChem CID: 15951529 ) | ||
Structure of Phytochemical |
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Structure of Anticancer Drug |
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2D
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MOL
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Pair Name | Lupeol, Enzalutamide | |||
Disease Info | [ICD-11: 2C82] | Prostate cancer | Investigative | |
Gene Regulation | Down-regulation | Expression | CFLAR | hsa8837 |
Down-regulation | Expression | HNF4A | hsa3172 | |
Down-regulation | Expression | MYC | hsa4609 | |
Down-regulation | Expression | PTEN | hsa5728 | |
In Vitro Model | PNT2 | Healthy | Homo sapiens (Human) | CVCL_2164 |
PC-3 | Prostate carcinoma | Homo sapiens (Human) | CVCL_0035 | |
PTEN-CaP8 | Carcinoma of the mouse prostate gland | Mus musculus (Mouse) | CVCL_0F37 | |
In Vivo Model | 1×10⁶ PTEN-CaP8 cells were introduced subcutaneously in the right flanks of mice. | |||
Result | Lupeol enhances the pharmacological efficacy of Enzalutamide and reduces the adverse effects. Thus, Lupeol could be a promising adjuvant for improving Enzalutamide-based treatment outcomes and warrant further research. |
No. | Title | Href |
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1 | Lupeol, an androgen receptor inhibitor, enhances the chemosensitivity of prostate cancer stem cells to antiandrogen enzalutamide-based therapy. Toxicol Appl Pharmacol. 2023 Nov 1;478:116699. doi: 10.1016/j.taap.2023.116699. | Click |