Phytochemical Name : Sesamol

Properties Information
PhytoCAT-ID PhytoCAT-1505
Phytochemical name or plant extracts Sesamol
PMID 34325508
Literature evidence Sesamol may be a safe and effective option for clinical adjuvant therapy in patients with ERα-negative breast cancer.
IUPAC name 1,3-benzodioxol-5-ol
Phytochemicals’ class or type of plant extracts Phenolic compound
Source of phytochemicals or plant Extracts Sesamum indicum
Geographical availability Assam, Bangladesh, India, West Himalaya
Plant parts Seeds
Other cancers Breast cancer
Target gene or protein pS2, GREB1, DNMT3A, DNMT3B, miR-370-3p
Gene or Protein evidence Sesamol induced ER? functional re-expression followed by upregulation of its downstream pS2 and GREB1 genes in ER?-negative breast carcinoma. Mechanistically, sesamol induced ESR1 gene promoter demethylation by downregulating the expression of the DNA methyltransferases DNMT3A and DNMT3B, without affecting DNMT1. Moreover, the non-coding RNA miR-370-3p directly targeted DNMT3A and DNMT3B mRNA, and its expression increased upon treatment with sesamol.
Target pathways NA
IC50 NA
Potency In summary, our study revealed that sesamol epigenetically induced ER? reactivation via miR-370-3p-mediated downregulation of DNMT3A and DNMT3B in ER-negative breast carcinoma models. These findings enhance the current knowledge on the biological properties of sesamol and show that this agent may be helpful for the clinical adjuvant treatment of patients with ER-negative breast cancer.
Cell line/ mice model MDA-MB-231, HUVEC and Hs-578T cells.
Additional information  In addition, miR-370-3p mimics downregulated DNMT3A and DNMT3B expression but not DNMT1, these effects were accompanied by reactivation of ER, pS2, and GREB1
PubChem ID 68289
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:675971-1
Safety NA