Properties |
Information |
PhytoCAT-ID |
PhytoCAT-696 |
Phytochemical name or plant extracts |
Pterostilbene |
PMID |
31004704 |
Literature evidence |
In addition, TMS activated the AHR more potently (EC50 in a reporter gene assay 2.0 μM) and induced AHR-mediated induction of cytochrome P450 1A1 (CYP1A1) activity (EC50 value of 0.7 μM) more than resveratrol and the other analogues tested. |
IUPAC name |
4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]phenol |
Phytochemicals’ class or type of plant extracts |
Stilbenoid |
Source of phytochemicals or plant Extracts |
Vitis rupestris |
|
Geographical availability |
Arkansas, District of Columbia, Hungary, Indiana, Kentucky, Maryland, Missouri, Oklahoma, Pennsylvania, Tennessee, Texas, Virginia, West Virginia |
Plant parts |
NA |
Other cancers |
Breast cancer, Lung cancer |
Target gene or protein |
Beclin-1, LC3 II, hTERT, cMyc, Cyclin D1, Rac1, WAVE-2, Arp2/3 |
Gene or Protein evidence |
Pterostilbene also caused a simultaneous increase in the expression autophagic marker proteins Beclin 1 and LC3 II (microtubule-associated protein 1 light chain 3) by approximately 6-folds, which leads to an alternative pathway of autophagy.Pterostilbene down-regulates hTERT at physiological concentrations in breast cancer cells: Potentially through the inhibition of cMyc. PT treatment regulated the protein expression of Cyclin D1 in TNBC and ER þ breast cancer cells, and also in the xenograft mouse model. In addition, pterostilbene significantly impaired the activity of Rac1 and the expression of WASP-family verprolin-homologous protein-2 (WAVE-2) and actin-related protein 2/3 (Arp2/3). |
Target pathways |
NF-κB-mediated uPA expression and Rac1/WAVE/Arp2/3 pathway |
IC50 |
45.7 μM against MDA-MB-231
63.1 μM against T-47D
|
Potency |
PT could point to a promising use against the development and the progression of breast cancer as a natural therapeutic agent. |
Cell line/ mice model |
MCF-7,MDA-MB-231 , T-47D, NCI H-460 |
Additional information |
Pterostilbene also led to phosphatidylserine externalization, internucleosomal DNA fragmentation, caspase activation and disruption of mitochondrial membrane potential. |
PubChem ID |
5281727 |
Additional PMIDs |
24433502 22273805 24304568 29125889 32900227 24440300 |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:69028-1 |
Safety |
NA |