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Salicylates and vascular smooth muscle cell proliferation: Molecular mechanisms for cell cycle arrest

Journal

TRENDS IN CARDIOVASCULAR MEDICINE
Volume 11, Issue 8, Pages 339-344

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/S1050-1738(01)00133-5

Keywords

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Funding

  1. NHLBI NIH HHS [HL-48743, HL-34836, HL-52233] Funding Source: Medline
  2. NINDS NIH HHS [NS-10828] Funding Source: Medline

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Salicylates are effective prophylactic treatment strategies for myocardial infarction and ischemic strokes. Recent evidence suggests that high doses of salicylates may exert direct, platelet-independent effects on the vascular wall. Salicylate and aspirin, in concentrations between 1 and 5 mM, effectively inhibit vascular smooth muscle cell proliferation and DNA synthesis without inducing cellular toxicity or apoptosis. This inhibition is associated with effects on specific cell-cycle regulatory molecules, and may proceed via downregulation of the transcription factor; nuclear factor (NF)-kappaB. High-dose salicylates and selective NF-kappaB inhibitors may, therefore, play an important role in the management of vascular proliferative disorders. (C) 2001, Elsevier Science Inc.

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