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dc.contributor.authorRudeewan Tungpraditen_US
dc.contributor.authorSupachok Sinchaikulen_US
dc.contributor.authorSuree Phutrakulen_US
dc.contributor.authorWeerah Wongkhamen_US
dc.contributor.authorShui Tein Chenen_US
dc.date.accessioned2018-09-04T04:17:48Z-
dc.date.available2018-09-04T04:17:48Z-
dc.date.issued2011-01-01en_US
dc.identifier.issn01252526en_US
dc.identifier.other2-s2.0-78649781090en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78649781090&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49765-
dc.description.abstractBerberine is the main cytotoxic compound in Coscinium fenestratum. Although, cytotoxic activity of berberine on many cancer cell lines have been studied but effect of berberine on NCI-H838 cell line is still not reported. In the present study, antiproliferative activity and mechanism of berberine isolated from C. fenestratum against NCI-H838 were investigated. NCI-H838 cells were treated with various concentrations of berberine and the cytotoxic activity was evaluated by MTT method. Berberine exhibited cytotoxicity by dose and time dependent manner with the IC50 values at 24, 48 and 72 h were 111.9±7.0 μM, 92.4±1.2 μM and 68.4±7.9 μM, respectively. Additionally, apoptotic in berberine treated cell was detected by DAPI staining. The associated proteins for apoptosis were examined by western blotting and it was found that berberine downregulated Bcl-2, procaspase 3, 6, 7 and 8 but upregulated caspase 7 by dose dependent manner. Moreover, berberine induced G2/M arrest was determined by the flow cytometric method. Taken together indicated that the potential of antiperiferal activity of berberine mediated through the Bcl-2/caspase-dependent pathway and G2/M cell cycle arrest.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.subjectMathematicsen_US
dc.subjectPhysics and Astronomyen_US
dc.titleAntiproliferative activity of berberine from Coscinium fenestratum on NCI-H838 cell lineen_US
dc.typeJournalen_US
article.title.sourcetitleChiang Mai Journal of Scienceen_US
article.volume38en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsAcademia Sinica Taiwanen_US
article.stream.affiliationsNational Taiwan Universityen_US
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