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DOI: 10.1055/s-2003-37501
J. A. Barth Verlag in Georg Thieme Verlag Stuttgart · New York
Statins Can Inhibit Proliferation of Human Breast Cancer Cells in Vitro
Publication History
Received: May 6, 2002
First decision: June 7, 2002
Accepted: July 17, 2002
Publication Date:
26 February 2003 (online)

Abstract
The effect of five statins, i.e. atorvastatin, fluvastatin, lovastatin, pravastatin and simvastatin was investigated on the proliferation of the human breast cancer cell line MCF-7. All statins except of pravastatin were able to inhibit cell proliferation up to 90 % at a concentration of 50 µM. Between the effective statins no significant difference was observed indicating a class-specific effect. These data suggest that statins may have clinical significance in the primary prevention of human breast cancer beyond their cholesterol-lowering effect. However, clinical proof must be awaited before drawing any further conclusions.
Key words
Statins - Cell proliferation - Human breast cancer cells
References
-
1 Andreotti P E, Thornthwaite J T, Morse I S.
ATP tumor chemosensitivity assay. Stanley PE, Kricka LJ Bioluminescence and Chemiluminescence: Current Status. Chichester; J. Wiley & Son 1991: 417-420 - 2 Denoyelle C, Vasse M, Korner M, Mishal Z, Ganne F, Vannier J P, Soria J, Soria C. Cerivastatin, an inhibitor of HMG-CoA reductase, inhibits the signaling pathway involved in the invasiveness and metastatic properties of highly invasive breast cancer cell lines: in vitro study. Carcinogenesis. 2001; 22 1139-48
- 3 Edwards P A, Ericsson J. Sterols and isoprenoids: signaling molecules derived from the cholesterol biosynthetic pathway. Annu Rev Biochem. 1999; 68 157-185
- 4 Gaw A, Packard C J, Shepherd J. Statins: The HMG CoA Reductase Inhibitors in Perspectives. London; Martin Dunitz 2000
- 5 Hamelin B A, Turgeon J. Hydophilicity/lipophilicity: relevance for the pharmacology and clinical effects of HMG-CoA reductase inhibitors. TiPS. 1998; 19 26-37
- 6 Hatanaka T. Clinical pharmacokinetics of pravastatin: mechanisms of pharmacokinetic events. Clin Pharmacokinet. 2000; 39 397-412
- 7 Lennernäs H, Fager G. Pharmacodynamics and pharmacokinetics of the HMG-CoA reductase inhibitors. Clin Pharmacokinet. 1997; 32 403-425
- 8 Mundy G, Garrett R, Harris S, Chan J, Chen D, Rossini G, Boyce B, Zhao M, Gutierrez G. Stimulation of bone formation in vitro and in rodents by statins. Science. 1999; 286 1946-1949
- 9 Simons M, Keller P. Cholesterol depletion inhibits the generation of beta-amyloid in hippocampal neurons. Proc Natl Acad Sci USA. 1998; 95 6460-6464
- 10 Takemoto M, Liao J K. Pleiotropic effects of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors. Arterioscler Thromb Vasc Biol. 2001; 21 1712-1719
MD, PhD, PH, Head of Section of Gynecological Endocrinology and Menopause A. O. Mueck
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