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DC Field | Value | Language |
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dc.contributor.author | Kanokkarn Phromnoi | en_US |
dc.contributor.author | Simone Reuter | en_US |
dc.contributor.author | Bokyung Sung | en_US |
dc.contributor.author | Pornngarm Limtrakul | en_US |
dc.contributor.author | Bharat B. Aggarwal | en_US |
dc.date.accessioned | 2018-09-04T04:42:07Z | - |
dc.date.available | 2018-09-04T04:42:07Z | - |
dc.date.issued | 2010-09-01 | en_US |
dc.identifier.issn | 02507005 | en_US |
dc.identifier.other | 2-s2.0-77958572996 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77958572996&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/50542 | - |
dc.description.abstract | We sought to determine the molecular basis for the anticancer activities of 5,3′-dihydroxy-3,6,7,8,4′-penta-methoxyflavone (DH-PMF), isolated from Gardenia obtusifolia traditionally used in Thailand for a variety of ailments. As little as 1 μM DH-PMF inhibited the proliferation of prostate, colon, kidney, lung, head and neck, pancreas, breast, leukemia, and myeloma cancer cell lines. DH-PMF also suppressed the colony-forming ability of tumor cells, with 50% inhibition occurring at a dose less than 10 nM. DH-PMF induced G2/M and subG1 cell cycle arrest, increased the levels of p21WAF1/CIP1 and p27KIP1, and reduced the expression of cyclin D1, CDC2, and c-MYC. Furthermore, DH-PMF inhibited AKT and glycogen synthase kinase 3 beta (GSK3β) activation, reduced cell survival proteins, and induced apoptosis, as indicated by annexin V staining, TUNEL assay, and activation of caspase-8, -9 and -3. Overall, our results demonstrate that DH-PMF induces suppression of cell proliferation through modulation of AKT-GSK3β pathways and induction of cyclin-dependent kinase (CDK) inhibitors. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Medicine | en_US |
dc.title | A dihydroxy-pentamethoxyflavone from Gardenia obtusifolia suppresses proliferation and promotes apoptosis of tumor cells through modulation of multiple cell signaling pathways | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Anticancer Research | en_US |
article.volume | 30 | en_US |
article.stream.affiliations | University of Texas MD Anderson Cancer Center | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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