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dc.contributor.authorPiyawan Bunpoen_US
dc.contributor.authorKeiko Kataokaen_US
dc.contributor.authorHideki Arimochien_US
dc.contributor.authorHaruyuki Nakayamaen_US
dc.contributor.authorTomomi Kuwaharaen_US
dc.contributor.authorUsanee Vinitketkumnuenen_US
dc.contributor.authorYoshinari Ohnishien_US
dc.date.accessioned2018-09-11T09:22:05Z-
dc.date.available2018-09-11T09:22:05Z-
dc.date.issued2005-02-01en_US
dc.identifier.issn13431420en_US
dc.identifier.other2-s2.0-15544366910en_US
dc.identifier.other10.2152/jmi.52.65en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=15544366910&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62116-
dc.description.abstractAsiatic acid is a pentacyclic triterpene contained in medicinal plants. The cytotoxic effect of this compound and its augmentative effect on the anticancer drug irinotecan hydrochloride (CPT-11) were investigated in the human colon adenocarcinoma cell line HT-29. Asiatic acid dose-dependently showed cytotoxicity in HT-29 cells. DNA fragmentation, annexin-positive apoptotic cells, and caspase-3 activation were observed in a dose-dependent manner. A caspase-3 inhibitor suppressed the DNA ladder formation in a concentration-dependent manner. Bcl-2 and Bcl-XL proteins were decreased by asiatic acid treatment. These results indicate that asiatic acid induced apoptosis in HT-29 cells via caspase-3 activation. Cytotoxic effects of combined treatment with CPT-11 and asiatic acid on HT-29 cells were further examined. Simultaneous treatment or sequential exposure first to asiatic acid and then to CPT-11 showed an additive effect. Synergism was observed when cells were first exposed to CPT-11 and then to asiatic acid. These results suggest that asiatic acid can be used as an agent for increasing sensitivity of colon cancer cells to treatment with CPT-11 or as an agent for reducing adverse effects of CPT-11.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleInhibitory effects of asiatic acid and CPT-11 on growth of HT-29 cellsen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Medical Investigationen_US
article.volume52en_US
article.stream.affiliationsTokushima Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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