Phytochemical Name : Kelussia odoratissima Mozaff. extract

Properties Information
PhytoCAT-ID PhytoCAT-637
Phytochemical name or plant extracts Kelussia odoratissima Mozaff. extract
PMID 28203057
Literature evidence It induced apoptosis, transduced the cell death signals, decreased the threshold of mitochondrial membrane potential (MMP), upregulated Bax and downregulated Bcl-2.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Methanolic extract
Source of phytochemicals or plant Extracts Kelussia odoratissima
Geographical availability Iran
Plant parts Whole plant
Other cancers Breast cancer
Target gene or protein Bax, Bcl-2, p21, p27
Gene or Protein evidence The upregulation of these proteins can stop the proliferation of the cells as indicated by our results, which show the upregulation of p21 and p27 after treatment with 8-hydroxy-ar-turmerone and KME in vitro and in vivo, respectively, while there was no significant expression in the cancer control group. Our data proposed that KME can initiate antiproliferative and apoptotic effects and destroy the tumor cells by disrupting the cell membrane and dysfunctioning the mitochondrial metabolic cascade, as well as disrupting the expression of Bax and Bcl-2 via the intrinsic pathway.
Target pathways NA
IC50 11.97±1.82 μg/mL against MCF-7
Potency This study demonstrated that K. odoratissima exhibits antitumor activity against breast cancer cells via cell death and cell cycle arrest.
Cell line/ mice model MCF-7, LA7, MCF-10A
Additional information  Our results demonstrated that K. odoratissima has an obvious effect on the arrest of proliferation of cancer cells.
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:60431916-2
Safety The results of the acute toxicity study show the nontoxic nature of KME, and the microscopic observation illustrates the glomeruli without signs of toxicity or fibrosis with normal hepatic lobules and renal ducts.