FASEB J. Pierce now sold as Thermo Scientific
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by ZIESCHE, R.
Right arrow Articles by BLOCK, L.-H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by ZIESCHE, R.
Right arrow Articles by BLOCK, L.-H.
(The FASEB Journal. 2004;18:1516-1523.)
© 2004 FASEB

The calcium channel blocker amlodipine exerts its anti-proliferative action via p21(Waf1/Cip1) gene activation

ROLF ZIESCHE*, VENTZISLAV PETKOV*, CHRISTOPHER LAMBERS*, PAUL ERNE{dagger} and LUTZ-HENNING BLOCK*,1

* Department of Internal Medicine IV, University of Vienna, Austria; and
{dagger} Department of Cardiology, Kantonsspital Luzern, Switzerland

1Correspondence: University Hospital Vienna, Department of Internal Medicine IV, Währinger Gürtel 18-20, A-1090 Vienna, Austria. E-mail: lutz-henning.block{at}akh-wien.ac.at

Proliferation of vascular smooth muscle cells (VSMC) contributes to the progression of atherosclerotic plaques. Calcium channel blockers have been shown to reduce VSMC proliferation, but the underlying molecular mechanism remains unclear. p21(Waf1/Cip1) is a potent inhibitor of cell cycle progression. Here, we demonstrate that amlodipine (10–6 to 10–8 M) activates de novo synthesis of p21(Waf1/Cip1) in vitro. We show that amlodipine-dependent activation of p21(Waf1/Cip1) involves the action of the glucocorticoid receptor (GR) and C/EBP-{alpha}. The underlying pathway apparently involves the action of mitogen-activated protein kinase or protein kinase C, but not of extracellular signal-related kinase or changes of intracellular calcium. Amlodipine-induced p21(Waf1/Cip1) promoter activity and expression were abrogated by C/EBP-{alpha} antisense oligonucleotide or by the GR antagonist RU486. Amlodipine-dependent inhibition of cell proliferation was partially reversed by RU486 at 10–8 M (58%±29%), antisense oligonucleotides targeting C/EBP-{alpha} (91%±26%), or antisense mRNAs targeting p21(Waf1/Cip1) (96%±32%, n=6); scrambled antisense oligonucleotides or those directed against C/EBP-ß were ineffective. The data suggest that the anti-proliferative action of amlodipine is achieved by induction of the p21 (Waf1/Cip1) gene, which may explain beneficial covert effects of this widely used cardiovascular therapeutic drug beyond a more limited role as a vascular relaxant.—Ziesche, R., Petkov, V., Lambers, C., Erne, P., Block, L.-H. The calcium channel blocker amlodipine exerts its anti-proliferative action via p21(Waf1/Cip1) gene activation.


Key Words: VSMC • glucocorticoid receptor • intracellular calcium • CCB







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by The Federation of American Societies for Experimental Biology.