Pair Name | Phenethyl isothiocyanate, Dibenzoylmethane | ||
Phytochemical Name | Phenethyl isothiocyanate (PubChem CID: 16741 ) | ||
Anticancer drug Name | Dibenzoylmethane (PubChem CID: 8433 ) | ||
Structure of Phytochemical |
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2D
MOL
3D
MOL
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Structure of Anticancer Drug |
Download
2D
MOL
3D
MOL
|
Pair Name | Phenethyl isothiocyanate, Dibenzoylmethane | |||
Disease Info | [ICD-11: 2C82] | Prostate cancer | Investigative | |
Biological Phenomena | Induction-->Apoptosis | |||
Gene Regulation | Down-regulation | Phosphorylation | AKT1 | hsa207 |
Down-regulation | Expression | BIRC5 | hsa332 | |
Down-regulation | Activity | CDH13 | hsa1012 | |
In Vitro Model | PC-3 | Prostate carcinoma | Homo sapiens (Human) | CVCL_0035 |
DU145 | Prostate carcinoma | Homo sapiens (Human) | CVCL_0105 | |
VCaP | Prostate carcinoma | Homo sapiens (Human) | CVCL_2235 | |
In Vivo Model | For a xenograft model, 2×10⁶ VCaP cells per 0.1 ml suspended in a mixture of Matrigel and RPMI 1640 medium (1 : 1) were injected subcutaneously into the back of the mice. | |||
Result | Our results indicate that administration of DBM and PEITC in combination may be an effective strategy for inhibiting/delaying the progression of prostate cancer to androgen independence. |
No. | Title | Href |
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1 | Phenethyl isothiocyanate in combination with dibenzoylmethane inhibits the androgen-independent growth of prostate cancer cells. Food Funct. 2018 Apr 25;9(4):2398-2408. doi: 10.1039/c7fo01983a. | Click |