Abstract Title:

Shikonin causes apoptosis by up-regulating p73 and down-regulating ICBP90 in human cancer cells.

Abstract Source:

Biochem Biophys Res Commun. 2015 Jul 30. Epub 2015 Jul 30. PMID: 26235879

Abstract Author(s):

Soon Young Jang, Darong Hong, Seo Young Jeong, Jong-Ho Kim

Article Affiliation:

Soon Young Jang


Shikonin, a natural naphthoquinone isolated from the Chinese traditional medicine Zi Cao (purple gromwell), is known to suppress the growth of several cancer cell types. In this study, we evaluated the pro-apoptotic effects of shikonin on MCF-7 and HeLa cells, and investigated the underlying mechanism. Shikonin-induced apoptosis was associated with activation of caspase-3, poly(ADP-ribose) polymerase (PARP) cleavage, up-regulation of p73, and down-regulation of BCL-2. Shikonin also induced up-regulation of the tumor suppressor gene, p16(INK4A). Increasing transcriptional activity of p16(INK4A) by shikonin treatment, we observed in luciferase promoter assay, reflects reduced promoter binding by down-regulation of ICBP90 (inverted CCAAT box binding protein, 90 kDa), which are involved in down-regulation of its partner, DNMT1 (DNA methyltransferase 1). On the basis of these results, we conclude that shikonin causes apoptosis via a p73-related, caspase-3-dependent pathway.

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