Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-1725 | |
Phytochemical name or plant extracts | Pleurotus ostreatus extracts | |
PMID | 19020765 | |
Literature evidence | Here, we identified as the most potent, P. ostreatus (oyster mushroom) which suppressed proliferation of breast cancer (MCF-7, MDA-MB-231) and colon cancer (HT-29, HCT-116) cells, without affecting proliferation of epithelial mammary MCF-10A and normal colon FHC cells. | |
IUPAC name | NA | |
Phytochemicals’ class or type of plant extracts | Extract | |
Source of phytochemicals or plant Extracts | Pleurotus ostreatus | |
Geographical availability | NA | |
Plant parts | NA | |
Other cancers | Breast cancer, Colon cancer | |
Target gene or protein | NA | |
Gene or Protein evidence | NA | |
Target pathways | These results indicate bioactive 6-linked glucans present in P. ostreatus extracts activate NK-cell cytotoxicity via regulation of activation and induction of IFNγ and NO..P. ostreatus suppresses the proliferation of breast and colon cancer cells via p53-dependent as well as p53-independent pathway. | |
IC50 | NA | |
Potency | In conclusion, our results indicated that the edible oyster mushroom has potential therapeutic/preventive effects on breast and colon cancer. | |
Cell line/ mice model | MCF-7, MDA-MB-231, HT-29, HCT-116 | |
Additional information | our data suggest that P. ostreatus significantly inhibits proliferation of human breast cancer cells MCF-7 and colon cancer cells HT-29 by G0/G1 cell cycle arrest. Therefore, P. ostreatus induces cell cycle arrest of MCF-7 by the up-regulation of the expression of p53 and p21, whereas cell cycle arrest of HT-29 is induced by the up-regulation of the expression of p21 | |
PubChem ID | NA | |
Additional PMIDs | NA | |
Additional sources of information | NA | |
Safety | NA |