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. |