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The effects of metformin and simvastatin on the growth of LNCaP and RWPE-1 prostate epithelial cell lines.
Pennanen, Pasi; Syvälä, Heimo; Bläuer, Merja; Savinainen, Kimmo; Ylikomi, Timo; Tammela, Teuvo L J; Murtola, Teemu J.
Afiliação
  • Pennanen P; University of Tampere, School of Medicine, Tampere, Finland. Electronic address: llpape@uta.fi.
  • Syvälä H; University of Tampere, School of Medicine, Department of Anatomy, Tampere, Finland.
  • Bläuer M; Tampere University Hospital, Department of Gastroenterology and Alimentary Tract Surgery and Tampere Pancreas Laboratory, Tampere, Finland.
  • Savinainen K; Pirkanmaa Hospital District/Science Center, Tampere, Finland.
  • Ylikomi T; University of Tampere School of Medicine, Department of Cell Biology, Tampere, Finland.
  • Tammela TLJ; University of Tampere, School of Medicine, Tampere, Finland; Tampere University Hospital, Department of Urology, Tampere, Finland.
  • Murtola TJ; University of Tampere, School of Medicine, Tampere, Finland; Tampere University Hospital, Department of Urology, Tampere, Finland.
Eur J Pharmacol ; 788: 160-167, 2016 Oct 05.
Article em En | MEDLINE | ID: mdl-27341997
ABSTRACT
The anti-diabetic drug metformin and cholesterol-lowering statins inhibit prostate cancer cell growth in vitro and have been linked with lowered risk of prostate cancer in epidemiological studies. We evaluated the effects of these drugs on cancerous and non-cancerous prostate epithelial cell lines. Cancer (LNCaP) and normal (RWPE-1) prostate epithelial cell lines were treated with pharmacologic concentrations of metformin and simvastatin alone and in combinations. Relative changes in cell number were measured with crystal violet staining method. Drug effects on apoptosis and cell cycle were measured with flow cytometry. We also measured changes in the activation and expression of a set of reported target proteins of metformin and statins with Western blotting. Metformin decreased the relative cell number of LNCaP cells by inducing G1 cell cycle block, autophagy and apoptosis, and slightly increased cytosolic ATP levels, whereas RWPE-1 cells were resistant to metformin. However, RWPE-1 cells were sensitive to simvastatin, which induced G2 cell cycle block, autophagy and apoptosis, and increased cytosolic ATP levels in these cells. Combination of metformin and simvastatin synergistically decreased cytosolic ATP levels, increased autophagy and instead of apoptosis, induced necrosis in LNCaP cells. Synergistic effects were not observed in RWPE-1 cells. These results suggest, that prostate cancer cells may be more vulnerable to combined growth-inhibiting effects of metformin and simvastatin compared to normal cells. The data presented here provide evidence for the potency of combined metformin and statin, also at pharmacologic concentrations, as a chemotherapeutic option for prostate cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Próstata / Sinvastatina / Células Epiteliais / Metformina Limite: Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Próstata / Sinvastatina / Células Epiteliais / Metformina Limite: Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article