Simvastatin impairs murine melanoma growth

• Published in: Lipids in health and disease Vol. 9; no. 1; p. 142
• Main Authors: Favero, Giovani M, F Otuki, Michel, Oliveira, Karen A, Bohatch, Jr, Milton S, Borelli, Primavera, Barros, Francisco E, Maria, Durvanei A, Fernandes, Daniel, Bydlowski, Sergio P
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 16-12-2010; BioMed Central; BMC
• Subjects: Animals; Antineoplastic Agents - therapeutic use; Apoptosis; Cell adhesion & migration; Cell Cycle - drug effects; Cell Line, Tumor; Cholesterol; Colleges & universities; Dosage and administration; Drug therapy; Enzymes; Experiments; Flow Cytometry; Liver - drug effects; Male; Melanoma; Melanoma - drug therapy; Melanoma - pathology; Mice; Mice, Inbred C57BL; Simvastatin; Simvastatin - therapeutic use; Spleen; Spleen - drug effects; Statins; Tumors; Brazil
• ISSN: 1476-511X; 1476-511X
• DOI: 10.1186/1476-511X-9-142

Statins induces cell cycle arrest, apoptosis, reduction of angiogenic factors, inhibition of the endothelial growth factor, impairing tissue adhesion and attenuation of the resistance mechanisms. The aim of this study was evaluate the anti-tumoral activity of simvastatin in a B16F10 melanoma-mouse model.
Melanoma cells were treated with different concentrations of simvastatin and assessed by viability methods. Melanoma cells (5 × 10(4)) were implanted in two month old C57Bl6/J mice. Around 7 days after cells injection, the oral treatments were started with simvastatin (5 mg/kg/day, p.o.). Tumor size, hematological and biochemical analyses were evaluated.
Simvastatin at a concentration of 0.8 μM, 1.2 μM and 1.6 μM had toxic effect. Concentration of 1.6 μM induced a massive death in the first 24 h of incubation. Simvastatin at 0.8 μM induces early cell cycle arrest in G0/G1, followed by increase of hypodiploidy. Tumor size were evaluated and the difference of treated group and control, after ten days, demonstrates that simvastatin inhibited the tumor expansion in 68%.
Simvastatin at 1.6 μM, presented cytototoxicity after 72 h of treatment, with an intense death. In vivo, simvastatin being potentially useful as an antiproliferative drug, with an impairment of growth after ten days.