Properties |
Information |
PhytoCAT-ID |
PhytoCAT-2160 |
Phytochemical name or plant extracts |
Paris saponin VII |
PMID |
24818584 |
Literature evidence |
Saponins of several herbs are known to induce apoptosis in some cancer cells and are proposed to be promising modulators of drug resistance. |
IUPAC name |
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8S,9S,12S,13R,16S)-8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol |
Phytochemicals’ class or type of plant extracts |
Saponin |
Source of phytochemicals or plant Extracts |
Trillium tschonoskii |
|
Geographical availability |
China North-Central, China South-Central, China Southeast, East Himalaya, Japan, Korea, Kuril Is., Myanmar, Sakhalin, Taiwan, Tibet |
Plant parts |
NA |
Other cancers |
Breast cancer |
Target gene or protein |
NFR1, TRAIL R1/DR4, TRAIL R2/DR5, FADD, PARP, Caspase 8, Caspase 3, P-gp |
Gene or Protein evidence |
Further results showed that PS VII treatment in MCF-7/ADR cells led to increased TNFR1, TRAIL R1/DR4, TRAIL R2/DR5, and FADD expression, and activation of PARP, caspase-8, and 3. In parallel to the alterations, P-glycoprotein expression and activity were also reduced. |
Target pathways |
NA |
IC50 |
NA |
Potency |
These findings showed that PS VII might be an effective tumouristatic agent for the treatment of MDR breast cancer. |
Cell line/ mice model |
MCF-7/ADR |
Additional information |
PS VII dose dependently suppressed cell viability as well as triggered apoptosis and modulated drug resistance of MCF-7/ADR cells. |
PubChem ID |
176233 |
Additional PMIDs |
30552993 |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:542611-1 |
Safety |
NA |