Phytochemical Name : 7α-hydroxy-β-sitosterol

Properties Information
PhytoCAT-ID PhytoCAT-585
Phytochemical name or plant extracts 7α-hydroxy-β-sitosterol
PMID 22997533
Literature evidence In continuation of our interest towards the elucidation of apoptotic pathways of cytotoxic phytocompounds, we have embarked upon a study on the anticancer effects of 7α-hydroxy-β-sitosterol (CT1), a rare natural phytosterol oxide isolated from Chisocheton tomentosus.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Phytosterols
Source of phytochemicals or plant Extracts Chisocheton tomentosus
Geographical availability Malaya, Thailand
Plant parts Bark
Other cancers Breast cancer, Cervical cancer, Oral cancer, Liver cancer
Target gene or protein Bax, Bcl-2, procaspase 9, procaspase 3, ERK1/2, FasL, Bim
Gene or Protein evidence CT1 was also found to increase proapoptotic Bax protein levels, while decreasing anti-apoptotic Bcl-2 protein levels, suggesting the involvement of the intrinsic pathway. Reduced levels of initiator procaspase-9 and executioner procaspase-3 were also observed following CT1 exposure, confirming the involvement of cytochrome c-mediated apoptosis via the mitochondrial pathway. CT1 Reduces ERK1/2, FasL, Bcl-2, and Bim Protein Levels
Target pathways ERK1/2 signaling pathway
IC50 38.2 ± 3.2 μM for 12h against MCF-7 28.6 ± 4.1 μM for 18h against MCF-7 16.0 ± 3.6 μM for 24h against MCF-7
Potency These results demonstrated the cytotoxic and apoptotic ability of 7α-hydroxy-β-sitosterol and suggest its potential anti-cancer use particularly on breast adenocarcinoma cells.
Cell line/ mice model MCF-7, HMEC, HSC-4, HepG2
Additional information  Our results showed that cell death in MCF-7 breast tumor cells was achieved through the induction of apoptosis via downregulation of the ERK1/2 signaling pathway.
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:577954-1
Safety NA