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pubmed-article:14577694pubmed:dateCreated2003-10-27lld:pubmed
pubmed-article:14577694pubmed:abstractText7,8-Dihydroxyflavanone, isolated from the seeds of Alpinia Katsumadai Hayata, showed an inhibitory effect on Jun-Fos dimer action. 7,8-Dihydroxyflavanone blocked the action of the dimer on a DNA consensus sequence, the AP-1 binding site. We have concluded that the Jun-Fos heterodimer, bound with 7,8-dihydroxyflavanone, cannot bind to the AP-1 site and therefore results in signal interruption. The 7,8-dihydroxyflavanone was also found to have an in vitro cytotoxic effect against A549 (a human lung cancer cell line) and K562 (a human leukemia cell line).lld:pubmed
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pubmed-article:14577694pubmed:authorpubmed-author:YangChul-HakC...lld:pubmed
pubmed-article:14577694pubmed:authorpubmed-author:HahmEun-Ryeon...lld:pubmed
pubmed-article:14577694pubmed:authorpubmed-author:ParkSeyeonSlld:pubmed
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pubmed-article:14577694pubmed:pagination431-6lld:pubmed
pubmed-article:14577694pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:14577694pubmed:year2003lld:pubmed
pubmed-article:14577694pubmed:articleTitle7, 8-dihydroxyflavanone as an inhibitor for Jun-Fos-DNA complex formation and its cytotoxic effect on cultured human cancer cells.lld:pubmed
pubmed-article:14577694pubmed:affiliationSchool of Chemistry and Molecular Engineering, College of Natural Sciences, Seoul National University, San 56-1, Shillim-dong, Kwanak-gu, Seoul, 151-742, Korea.lld:pubmed
pubmed-article:14577694pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:14577694pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed