Phytochemical Name : Gomisin J

Properties Information
PhytoCAT-ID PhytoCAT-652
Phytochemical name or plant extracts Gomisin J
PMID 30542721
Literature evidence In attempting to identify effective anticancer drugs from natural products that are harmless to humans, we found that the gomisin J from Schisandra chinensis fruit has anticancer activity.
IUPAC name (9R,10S)-3,4,15,16-tetramethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-5,14-diol
Phytochemicals’ class or type of plant extracts Lignan
Source of phytochemicals or plant Extracts Schisandra chinensis
Geographical availability Amur, China North-Central, Inner Mongolia, Japan, Khabarovsk, Korea, Manchuria, Primorye, Sakhalin
Plant parts Fruit
Other cancers Breast cancer, Colon cancer, Cervical cancer
Target gene or protein p62, SQSTM1, LC3-I
Gene or Protein evidence Gomisin J treatment started to only slightly induce the decrease of p62/SQSTM1 expression level and the conversion from LC3-I to LC3-II after 24 h, but significantly after longer exposure of 72 h
Target pathways PI3K/AKT/mTOR pathway
IC50 NA
Potency In an extended study, gomisin J exhibited a strong cytotoxic effect on all tested various types of 13 cancer cell lines, indicating its potential to be used against a wide range of different types of cancer cells.
Cell line/ mice model MCF-7, MDA-MB-231, BT-20, BT-549, T47D, SKBR-3, MDA-MB-453, HS578T, MDA-MB-468, HCT116, HT-29, HeLa, SiHa
Additional information  Our data also revealed that gomisin J induced necroptosis, a programmed form of necrosis, as well as apoptosis. Notably, gomisin J predominantly induced necroptosis in MCF7 cells that are known to have high resistance to many pro-apoptotic anticancer drugs, while MDA-MB-231 exhibited a much lower level of necroptosis but instead a higher level of apoptosis.
PubChem ID 3001686
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:60456331-2
Safety Our data revealed that gomisin J exerted a much stronger cytotoxic effect on MCF7 and MDA-MB-231 cancer cells than on MCF10A normal cells.