β-Hydroxyisovalerylshikonin induces apoptosis in human leukemia cells by inhibiting the activity of a polo-like kinase 1 (PLK1)

β -Hydroxyisovalerylshikonin ( β -HIVS), which was isolated from the plant, Lithospermum radix , induces apoptosis in various lines of human tumor cells. To identify genes involved in β -HIVS-induced apoptotic process, we performed cDNA array analysis and found that β -HIVS suppresses the expression...

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Veröffentlicht in:Oncogene 2003-02, Vol.22 (7), p.1012-1023
Hauptverfasser: Masuda, Yutaka, Nishida, Ayano, Hori, Kouichi, Hirabayashi, Takahiro, Kajimoto, Sachiko, Nakajo, Shigeo, Kondo, Takeshi, Asaka, Masahiro, Nakaya, Kazuyasu
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Sprache:eng
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Zusammenfassung:β -Hydroxyisovalerylshikonin ( β -HIVS), which was isolated from the plant, Lithospermum radix , induces apoptosis in various lines of human tumor cells. To identify genes involved in β -HIVS-induced apoptotic process, we performed cDNA array analysis and found that β -HIVS suppresses the expression of the gene for a polo-like kinase 1 (PLK1) that is involved in control of the cell cycle. When U937 and HL60 cells were treated with 10 −6   M β -HIVS for 0.5 h, both the amount of PLK1 itself and the kinase activity of this enzyme were decreased. By contrast, Bcr–Abl-positive K562 cells were resistant to the induction of apoptosis by β -HIVS and this compound did not suppress the kinase activity of PLK1 in these cells. However, simultaneous treatment of K562 cells with both β -HIVS and STI571, which selectively inhibits the protein tyrosine kinase (PTK) activity of Bcr–Abl, strongly induced apoptosis. Moreover, β -HIVS increased the inhibitory effect of STI571 on PTK activity. Treatment of K562 cells with antisense oligodeoxynucleotides (ODNs) specific for PLK1 sensitized these cells to the β -HIVS-induced fragmentation of DNA. These results suggest that suppression of the activity of PLK1 via inhibition of tyrosine kinase activity by β -HIVS might play a critical role in the induction of apoptosis.
ISSN:0950-9232
1476-5594
DOI:10.1038/sj.onc.1206200