Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49739
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dc.contributor.authorKanokkarn Phromnoien_US
dc.contributor.authorSimone Reuteren_US
dc.contributor.authorBokyung Sungen_US
dc.contributor.authorSahdeo Prasaden_US
dc.contributor.authorRamaswamy Kannappanen_US
dc.contributor.authorVivek R. Yadaven_US
dc.contributor.authorWisinee Chanmahasathienen_US
dc.contributor.authorPornngarm Limtrakulen_US
dc.contributor.authorBharat B. Aggarwalen_US
dc.date.accessioned2018-09-04T04:17:27Z-
dc.date.available2018-09-04T04:17:27Z-
dc.date.issued2011-02-01en_US
dc.identifier.issn15210111en_US
dc.identifier.issn0026895Xen_US
dc.identifier.other2-s2.0-78751533767en_US
dc.identifier.other10.1124/mol.110.067512en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78751533767&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49739-
dc.description.abstractMost anticancer drugs have their origin in traditional medicinal plants. We describe here a flavone, 5,3′-dihydroxy-3,6,7,8,4′- pentamethoxyflavone (PMF), from the leaves of the Thai plant Gardenia obtusifolia, that has anti-inflammatory and anticancer potential. Because the nuclear factor-κB (NF-κB) pathway is linked to inflammation and tumorigenesis, we investigated the effect of PMF on this pathway. We found that PMF suppressed NF-κB activation induced by inflammatory agents, tumor promoters, and carcinogens. This suppression was not specific to the cell type. Although PMF did not directly modify the ability of NF-κB proteins to bind to DNA, it inhibited IκBα (inhibitory subunit of NF-κB) kinase, leading to suppression of phosphorylation and degradation of IκBα, and suppressed consequent p65 nuclear translocation, thus abrogating NF-κB-dependent reporter gene expression. Suppression of the NF-κB cell signaling pathway by the flavone led to the inhibition of expression of NF-κB-regulated gene products that mediate inflammation (cyclooxygenase-2), survival (XIAP, survivin, Bcl-xL, and cFLIP), proliferation (cyclin D1), invasion (matrix metalloproteinase-9), and angiogenesis (vascular endothelial growth factor). Suppression of antiapoptotic gene products by PMF correlated with the enhancement of apoptosis induced by tumor necrosis factor-α and the chemotherapeutic agents cisplatin, paclitaxel, and 5-flurouracil. Overall, our results indicate that PMF suppresses the activation of NF-κB and NF-κB-regulated gene expression, leading to the enhancement of apoptosis. This is the first report to demonstrate that this novel flavone has anti-inflammatory and anticancer effects by targeting the IKK complex. Copyright © 2011 The American Society for Pharmacology and Experimental Therapeutics.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA novel pentamethoxyflavone down-regulates tumor cell survival and proliferative and angiogenic gene products through inhibition of IκB kinase activation and sensitizes tumor cells to apoptosis by cytokines and chemotherapeutic agentsen_US
dc.typeJournalen_US
article.title.sourcetitleMolecular Pharmacologyen_US
article.volume79en_US
article.stream.affiliationsUniversity of Texas MD Anderson Cancer Centeren_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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