Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Takeuchi, N.
Right arrow Articles by Yamamura, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Takeuchi, N.
Right arrow Articles by Yamamura, H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

J. Biochem, 1992, Vol. 112, No. 6 762-767
© 1992 Japanese Biochemical Society


research-article

Inhibitory Effect of Mitoxantrone on Activity of Protein Kinase C and Growth of HL60 Cells1

Noriko Takeuchi*, Toru Nakamura*, Fumito Takeuchi**, Eikichi Hashimoto** and Hirohei Yamamura**

*Department of Internal Medicine, Fukui Medical School Matsuoka, Fukui 910-11
**Department of Biochemistry, Fukui Medical School Matsuoka, Fukui 910-11

Mitoxantrone, a new anthraquinone, showed inhibitory an effect on protein kinase C (PKC) activity. Its IC50, value was 4.4 µg/ml (8.5 µM), which is much lower than those of the well-known anthracyclines daunorubicin and doxorubicin, the IC50, values of which are more. than 100 µg/ml (> 170 µM). Kinetic studies demonstrated that mitoxantrone inhibited PKC in a competitive manner with respect to histone H1, and its K1 value was 6.3 µM (K1 values of daunorubicin and doxorubicin were 0.89 and 0.15 mM, respectively), and in a non-competitive manner with respect to phosphatidylserine and ATP. Inhibition of phosphorylation by mitoxantrone was observed with various substrates including S6 peptide, myelin basic protein and its peptide substrate derived from the amino-terminal region. Their IC50 values were 0.49 µg/ml (0.95 µM), 1.8 µg/ml (3.5 µM), and 0.82 µg/ml (1.8 µM), respectively. Mitoxantrone did not markedly inhibit the activity of cyclic AMP-dependent protein kinase, casein kinase I or casein kinase II, at concentrations of less than 10 µg/ml. On the other hand, brief exposure (5 min) of HL60 cells to mitoxantrone caused the inhibition of cell growth with an IC50 value of 52 ng/ml (0.1 µM). In HL60 cells, most of the PKC activity (about 90%) was deteded in the cytosolic fraction. When HL60 cells exposed to 10 µg/ml mitoxantrone for 5 min were observed with fluorescence microscopy, the fluorescence elicited from mitoxantrone was detected in the extranuclear area. These results indicated that mitoxantrone is a potent inhibitor of PKC, and this inhibition may be one of the mechanisms of antitumor activity of mitoxantrone.

1This work was supported in part by Grants-in-Aid for General Scientific Research from the Ministry of Education. Science and Culture and for Cancer Research from the Ministry of Health and Welfare of Japan.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.