Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-1319 | |
Phytochemical name or plant extracts | Alisma canaliculatum extract | |
PMID | 30177620 | |
Literature evidence | Our results suggest that ACE has potential as a herbal supplement for the inhibition of breast cancer metastasis. | |
IUPAC name | NA | |
Phytochemicals’ class or type of plant extracts | Ethanolic extract | |
Source of phytochemicals or plant Extracts | Alisma canaliculatum | |
Geographical availability | China North-Central, China South-Central, China Southeast, Japan, Korea, Kuril Is., Nansei-shoto, Taiwan | |
Plant parts | Root | |
Other cancers | Breast cancer | |
Target gene or protein | CXCR3, CXCL10, IKK-NF-kappaB | |
Gene or Protein evidence | These results suggest that ACE abrogates TNFα-induced migration of MDA-MB-231 breast cancer cells through down-regulation of IKK-NF-kappaB-dependent CXCR3 and CXCL10 expression. | |
Target pathways | ACE prevents TNFα-induced Migration of MDA-MB-231 metastatic breast cancer cells and inhibits TNFα-induced CXCR3 and CXCL10 expression through inhibition of the I?B kinase (IKK)-mediated NF-kappaB pathway. | |
IC50 | NA | |
Potency | NA | |
Cell line/ mice model | MDA-MB-231 | |
Additional information | ACE inhibits TNFα-induced phosphorylation of inhibitor of ?B (I?B) kinase (IKK), I?B and p65/RelA, leading to the suppression of nuclear translocation of p65/RelA nuclear factor kappa-B (NF-kappaB). Also, ACE inhibited NF-kappaB-dependent CXCR3 and CXCL10 promoter activities. | |
PubChem ID | NA | |
Additional PMIDs | NA | |
Additional sources of information | https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:327944-2 | |
Safety | NA |