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dc.contributor.authorJie Zhangen_US
dc.contributor.authorWan fang Zhuen_US
dc.contributor.authorJian Xuen_US
dc.contributor.authorWorapong Kitdamrongthamen_US
dc.contributor.authorAranya Manosroien_US
dc.contributor.authorJiradej Manosroien_US
dc.contributor.authorHarukuni Tokudaen_US
dc.contributor.authorMasahiko Abeen_US
dc.contributor.authorToshihiro Akihisaen_US
dc.contributor.authorFeng Fengen_US
dc.date.accessioned2018-09-05T04:38:11Z-
dc.date.available2018-09-05T04:38:11Z-
dc.date.issued2018-03-25en_US
dc.identifier.issn18727573en_US
dc.identifier.issn03788741en_US
dc.identifier.other2-s2.0-85038012595en_US
dc.identifier.other10.1016/j.jep.2017.11.016en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85038012595&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59101-
dc.description.abstract© 2017 Elsevier B.V. Ethnopharmacological relevance Ficus hispida L.f. (Moraceae) has been used as alternative for traditional medicine in the treatment of various ailments including cancer-cure. The aim of this study was to evaluate the cancer chemopreventive and anticancer activities of crude extracts of F. hispida, with the objective to screen the inhibition of Epstein–Barr virus early antigen, and cytotoxic active components, and provide foundation for potential applications of this promising medical plant. Materials and methods Compounds were isolated from the MeOH extract of F. hispida fruits, and their structure elucidation was performed on the basis of extensive spectroscopic analysis. The isolated compounds were evaluated for their inhibitory activities against the Epstein–Barr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol 13-acetate (TPA) in Raji cells, and cytotoxic activities against human cancer cell lines (HL60, A549, SKBR3, KB, Hela, HT29, and HepG2) and a normal cell (LO2) using MTT method. For the compound with potent cytotoxic activity, its apoptosis inducing activity was evaluated by the observation of ROS generation level expression, and membrane phospholipid exposure and DNA fragmentation in flow cytometry. The mechanisms of the apoptosis induction were analyzed by Western blotting. Results Nineteen compounds, 1–19, including two new isoflavones, 3′-formyl-5,7-dihydroxy-4′-methoxyisoflavone (2) and 5,7-dihydroxy-4′-methoxy-3′- (3-methyl-2-hydroxybuten-3-yl)isoflavone (3), were isolated from the MeOH extract of F. hispida fruits. Five compounds, isowigtheone hydrate (1), 2, 3, 9, and 19, showed potent inhibitory effects on EBV-EA induction with IC50values in the range of 271–340 molar ratio 32 pmol−1TPA. In addition, five phenolic compounds, 1–3, 10, and 13, exhibited cytotoxic activity against two or more cell lines (IC502.5–95.8 μM), as well as compounds 1 and 3 were also displayed high selectivity for LO2/HepG2 (SI 23.5 and 11.8, respectively), while the compound 1-induced ROS generation leads to activated caspases-3, −8, and −9 apoptotic process in HL60 cells. Conclusion This study has established that the MeOH extract of F. hispida fruits contains isoflavones, coumarins, caffeoylquinic acids, along with other compounds including phenolics and steroid glucoside as active principles, and has demonstrated that the chemical constituents of F. hispida may be valuable as potential chemopreventive and anticancer agents.en_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titlePotential cancer chemopreventive and anticancer constituents from the fruits of Ficus hispida L.f. (Moraceae)en_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Ethnopharmacologyen_US
article.volume214en_US
article.stream.affiliationsChina Pharmaceutical Universityen_US
article.stream.affiliationsJiangsu Food and Pharmaceutical Science Collegeen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsKyoto Universityen_US
article.stream.affiliationsTokyo University of Scienceen_US
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