Phytochemical Name : Selenium (Se)-containing polysaccharides

Properties Information
PhytoCAT-ID PhytoCAT-762
Phytochemical name or plant extracts Selenium (Se)-containing polysaccharides
PMID 27865619
Literature evidence It is concluded that Se-containing polysaccharides from P. fortuneana potently inhibit the growth and induce apoptosis of TNBC cells and can be potential anticancer agent for TNBC.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Polysaccharide
Source of phytochemicals or plant Extracts Pyracantha fortuneana
Geographical availability Assam, China North-Central, China South-Central, China Southeast, East Himalaya, India, Myanmar, Nepal, Pakistan, Tibet, Vietnam, West Himalaya
Plant parts NA
Other cancers Breast cancer
Target gene or protein p53, Bax, PUMA, Noxa, Bcl-2, Bax, Caspase 3, Caspase 9, p53
Gene or Protein evidence In vitro studies showed that treatment of triple negative breast cancer (TNBC) MDA-MB-231 cells with Se-PFPs (1) inhibited cell growth dose-dependently by arresting cells at G2 phase via inhibiting CDC25C-CyclinB1/CDC2 pathway, (2) caused apoptosis associated with increased p53, Bax, Puma and Noxa, decreased Bcl2, increased Bax/Bcl2 ratio and increased activities of caspases 3/9, suggesting its effect on p53-mediated cytochrome c-caspase pathway
Target pathways p53-mediated cytochrome c-caspase pathway CDC25C-CyclinB1/CDC2 pathway
IC50 NA
Potency It is concluded that Se-containing polysaccharides from P. fortuneana potently inhibit the growth and induce apoptosis of TNBC cells and can be potential anticancer agent for TNBC.
Cell line/ mice model MDA-MB-231
Additional information  This extract contained 93.7% (w/w) of carbohydrate, 2.1% (w/w) of uronic acid and 3.7μg/g of Se, and was considered as Se-conjugated polysaccharides (Se-PFPs).
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:730613-1
Safety Treatment of nude mice bearing MDA-MB-231-derived xenograft tumors with Se-PFPs significantly reduced tumor growth without altering body weight, confirming its antitumor activity without toxic side effects.