Anti-proliferative effect of honokiol in oral squamous cancer through the regulation of specificity protein 1

Honokiol (HK), a novel plant-derived natural product, is a physiologically activated compound with polyphenolic structure, and has been identified to function as an anticancer agent. It has been widely used in several diseases as a traditional medicine for a long time. We investigated whether HK cou...

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Veröffentlicht in:International journal of oncology 2013-10, Vol.43 (4), p.1103-1110
Hauptverfasser: KIM, DONG-WOOK, KO, SEON MI, JEON, YOUNG-JOO, NOH, YOUNG-WOOCK, CHOI, NAG-JIN, CHO, SUNG-DAE, MOON, HONG SEOP, CHO, YOUNG SIK, SHIN, JAE-CHEN, PARK, SEON-MIN, SEO, KANG SEOK, CHOI, JI-YOUNG, CHAE, JUNG-IL, SHIM, JUNG-HYUN
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Sprache:eng
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Zusammenfassung:Honokiol (HK), a novel plant-derived natural product, is a physiologically activated compound with polyphenolic structure, and has been identified to function as an anticancer agent. It has been widely used in several diseases as a traditional medicine for a long time. We investigated whether HK could show anticancer effects on two oral squamous cell lines (OSCCs), HN-22 and HSC-4. We demonstrated that HK-treated cells showed dramatic reduction in cell growth and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly inhibited by HK in a dose-dependent manner. Furthermore, we checked changes in cell cycle regulatory proteins and anti-apoptotic proteins at the molecular level, which are known as Sp1 target genes. The important key regulators in the cell cycle such as p27 and p21 were up-regulated by HK-mediated down-regulation of Sp1, whereas anti-apoptotic proteins including Mcl-1 and survivin were decreased, resulting in caspase-dependent apoptosis. Taken together, results from this study suggest that HK could modulate Sp1 transactivation and induce apoptotic cell death through the regulation of cell cycle and suppression of anti-apoptotic proteins. In addition, HK may be used in cancer prevention and therapies to improve the clinical outcome as an anticancer drug.
ISSN:1019-6439
1791-2423
DOI:10.3892/ijo.2013.2028