Properties |
Information |
PhytoCAT-ID |
PhytoCAT-1002 |
Phytochemical name or plant extracts |
Evodiamine |
PMID |
25621054 |
Literature evidence |
Evodiamine is extracted from a variety of traditional Chinese medicines, which has been reported to induce apoptosis in certain tumors, including cervical, prostate and breast cancer, however, its effect on oestosarcoma cells remains unclear. |
IUPAC name |
(1S)-21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15,17,19-heptaen-14-one |
Phytochemicals’ class or type of plant extracts |
Alkaloid |
Source of phytochemicals or plant Extracts |
Evodia rutaecarpa |
|
Geographical availability |
E. Asia - China to the Himalayas. |
Plant parts |
Fruits |
Other cancers |
Breast cancer, Cervical cancer, Skin cancer, Leukemia |
Target gene or protein |
MMP9, uPA, uPAR, ERK, p38 MAPK, topo I, Bax, Bcl-2, Caspase 3, Survivin |
Gene or Protein evidence |
In vitro, evodiamine inhibited cell migration and invasion abilities through downregulation of MMP-9, urokinase-type plasminogen activator (uPA) and uPAR expression. Moreover, evodiamine regulated p-ERK and p-p38 MAPK expression. Herein, we report using a scaffold-hopping approach to identify a series of novel polycyclic heterocyclic derivatives based on Evo as the topoisomerase I (Top1) inhibitor for the treatment of triple-negative breast cancer (TNBC), which is an aggressive subtype of breast cancer with limited treatment options. evodiamine downregulated the expression of Bcl-2, caspase-3 and survivin, and upregulated the expression of Bax in human osteosarcoma cells. |
Target pathways |
ER-inhibitory pathway, aspase-dependent pathway, Ras/MEK/ERK pathway |
IC50 |
NA |
Potency |
These results demonstrate that evodiamine possesses antitumor activities via inhibition of cell migration and invasion, arrest of the cell cycle and induction of cell apoptosis in MDA-MB-231 cells. |
Cell line/ mice model |
MDA-MB-231, MCF-7, A375-S2, HeLa, THP-1, L929 |
Additional information |
The combination of berberine and evodiamine synergistically inhibited tumor growth in vivo in MCF-7 human breast cancer xenografts.
Evodiamine synergizes with doxorubicin in the treatment of chemoresistant human breast cancer without inhibiting P-glycoprotein. |
PubChem ID |
442088 |
Additional PMIDs |
24904975 23840656 25621054 23708383 14989376 24830744 29061795 19384267 34844412 30588834 24103429 |
Additional sources of information |
https://pfaf.org/User/Plant.aspx?LatinName=Euodia+ruticarpa |
Safety |
NA |