Properties |
Information |
PhytoCAT-ID |
PhytoCAT-1923 |
Phytochemical name or plant extracts |
Gomisin G |
PMID |
29587339 |
Literature evidence |
To investigate the molecular mechanism of this activity, we examined the signal transduction pathways after treatment with Gomisin G in MDA-MB-231 cells. |
IUPAC name |
[(9S,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate |
Phytochemicals’ class or type of plant extracts |
Lignan |
Source of phytochemicals or plant Extracts |
Schisandra chinesis |
|
Geographical availability |
Amur, China North-Central, Inner Mongolia, Japan, Khabarovsk, Korea, Manchuria, Primorye, Sakhalin |
Plant parts |
Fruits |
Other cancers |
Breast cancer |
Target gene or protein |
AKT phosphorylation, retinoblastoma tumor suppressor (Rb), phosphorylated Rb, Cyclin D1 |
Gene or Protein evidence |
Gomisin G did not induce apoptosis but drastically inhibited AKT phosphorylation and reduced the amount of retinoblastoma tumor suppressor protein (Rb) and phosphorylated Rb. Gomisin G induced in a proteasome-dependent manner a decrease in Cyclin D1. |
Target pathways |
NA |
IC50 |
NA |
Potency |
Treatment with Gomisin G suppressed the viability of two TNBC cell lines, MDA-MB-231 and MDA-MB-468 but not non-TNBC cell lines such as MCF-7, T47D, and ZR75-1. |
Cell line/ mice model |
MDA-MB-231 and MDA-MB-468 |
Additional information |
These results show that Gomisin G has an anti-cancer activity by suppressing proliferation rather than inducing apoptosis in TNBC cells.
Our study suggests that Gomisin G could be used as a therapeutic agent in the treatment of TNBC patients |
PubChem ID |
14992067 |
Additional PMIDs |
NA |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:60456331-2 |
Safety |
NA |