Properties |
Information |
PhytoCAT-ID |
PhytoCAT-1735 |
Phytochemical name or plant extracts |
Deoxyelephantopin |
PMID |
20105176 |
Literature evidence |
Moreover, tumour necrosis factor alpha-induced matrix metalloproteinase-9 enzyme activity and expression and nuclear factor-kappa B activation were abolished by DET. |
IUPAC name |
[(3S,4R,8R,9E,12R)-10-methyl-5-methylidene-6,14-dioxo-7,13-dioxatricyclo[10.2.1.04,8]pentadeca-1(15),9-dien-3-yl] 2-methylprop-2-enoate |
Phytochemicals’ class or type of plant extracts |
Sesquiterpene lactone |
Source of phytochemicals or plant Extracts |
Elephantopus scaber |
|
Geographical availability |
Andaman Is., Angola, Assam, Bangladesh, Cambodia, Cameroon, China South-Central, China Southeast, Comoros, East Himalaya, Hainan, India, Jawa, Laos, Madagascar, Malaya, Mozambique, Myanmar, Nansei-shoto, Nepal, Nicobar Is., Sri Lanka, Taiwan, Tanzania, Thailand, Vietnam, Zambia, Zaïre, Zimbabwe |
Plant parts |
NA |
Other cancers |
Breast cancer |
Target gene or protein |
p21(Waf1/Cip1), MMP9, NF-kB |
Gene or Protein evidence |
c-Jun N-terminal kinase-mediated p21(Waf1/Cip1) expression and caspase activation cascades were up-regulated by DET, effects suppressed by N-acetyl-L-cysteine. Moreover, tumour necrosis factor alpha-induced matrix metalloproteinase-9 enzyme activity and expression and nuclear factor-kappa B activation were abolished by DET. Pretreatment with DET was more effective than paclitaxel, for profound suppression of orthotopic tumour growth (99% vs. 68% reduction in tumour size) and lung metastasis of TS/A cells (82% vs. 63% reduction in metastatic pulmonary foci) and prolonged median survival time (56 vs. 37 days, P < 0.01) in mice. |
Target pathways |
NA |
IC50 |
11.24 μM against MDA-MB-231 |
Potency |
Our data provide evidence for the suppression of mammary adenocarcinoma by DET with several mechanisms and suggest that DET has potential as a chemopreventive agent for breast cancer. |
Cell line/ mice model |
MDA-MB-231, MCF-7 |
Additional information |
1) Quantitative proteome analysis of TNBC cell-secreted exosomes showed that DET and DETD-35 attenuated the expression of proteins related to cell migration, cell adhesion, and angiogenesis.
2)DET and DETD-35 induced reactive oxygen species (ROS) which caused structural damage and dysfunction of mitochondria and increased cytosolic calcium level, subsequently evoking exosome release from the cancer cells. |
PubChem ID |
6325056 |
Additional PMIDs |
24963325 28706483 20105176 28915644 |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:202958-1 |
Safety |
NA |