Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-133 | |
Phytochemical name or plant extracts | Chicory's extract | |
PMID | 22812448 | |
Literature evidence | Introducing Cichorium Pumilum as a potential therapeutical agent against drug-induced benign breast tumor in rats. | |
IUPAC name | NA | |
Phytochemicals’ class or type of plant extracts | Extract | |
Source of phytochemicals or plant Extracts | Cichorium Pumilum | |
Geographical availability | Afghanistan, Albania, Algeria, Azores, Baleares, Belgium, Bulgaria, Canary Is., Corse, Cyprus, East Aegean Is., Egypt, France, Greece, Gulf States, Iran, Iraq, Italy, Kriti, Lebanon-Syria, Libya, Madeira, Morocco, Palestine, Portugal, Romania, Sardegna, Saudi Arabia, Sicilia, Sinai, Spain, Switzerland, Transcaucasus, Tunisia, Turkey, Turkey-in-Europe, Western Sahara, Xinjiang, Yugoslavia | |
Plant parts | Aerial parts | |
Other cancers | Breast cancer | |
Target gene or protein | NA | |
Gene or Protein evidence | NA | |
Target pathways | NA | |
IC50 | NA | |
Potency | These results suggest that chicory extracts could be used as herbal photosensitizing agent in treating benign breast tumor in rats. | |
Cell line/ mice model | Female Sprague-Dawley rats | |
Additional information | Chicory's extract has significantly increase P.carbonyl (PC) and malondialdehyde (MDA) and decreases the hepatic levels of total antioxidant capacity (TAC) and superoxide dismutase (SOD) in benign breast tumors-induced group compared to control. It also significantly decrease the number of estrogen receptors ER-positive cells in tumor masses. | |
PubChem ID | NA | |
Additional PMIDs | NA | |
Additional sources of information | https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:194540-1 | |
Safety | NA |