Anti-angiogenic and anti-inflammatory effects of statins:: Relevance to anti-cancer therapy

被引:191
作者
Dulak, J [1 ]
Józkowicz, A [1 ]
机构
[1] Jagiellonian Univ, Fac Biotechnol, Dept Med Biotechnol, PL-30387 Krakow, Poland
基金
英国惠康基金;
关键词
vascular endothelial growth factor; 3-hydroxy-3-methylglutaryl-coenzyme A reductase; nitric oxide; heme oxygenase; apoptosis; endothelium; atherosclerosis; hypercholesterolemia;
D O I
10.2174/156800905774932824
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis is indispensable for the growth of solid tumors and angiogenic factors are also involved in the progression of hematological malignancies. Targeting the formation of blood vessels is therefore regarded as a promising strategy in cancer therapy. Interestingly, besides demonstration of some beneficial effects of novel anti-angiogenic compounds, recent data on the activity of already available drugs point to their potential application in anti-angiogenic therapy. Among these are the statins, the inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase. Statins are very efficient in the treatment of hypercholesterolemia in cardiovascular disorders; however, their effects are pleiotropic and some are not directly related to the inhibition of cholesterol synthesis. Some reports particularly highlight the pro-angiogenic effects of statins, which are caused by low, nanomolar concentrations and are regarded as beneficial for the treatment of cardiovascular diseases. On the other hand, the anti-angiogenic activities, observed at micromolar concentrations of statins, may be of special significance for cancer therapy. Those effects are caused by the inhibition of both proliferation and migration and induction of apoptosis in endothelial cells. Moreover, the statin-mediated inhibition of vascular endothelial growth factor synthesis, the major angiogenic mediator, may contribute to the attenuation of angiogenesis. It has been suggested that the anti-cancer effect of statins can be potentially exploited for the cancer therapy. However, several clinical trials aimed at the inhibition of tumor growth by treatment with very high doses of statins did not provide conclusive data. Herein, the reasons for those outcomes are discussed and the rationale for further studies is presented.
引用
收藏
页码:579 / 594
页数:16
相关论文
共 170 条
[61]   Molecular regulation of vessel maturation [J].
Jain, RK .
NATURE MEDICINE, 2003, 9 (06) :685-693
[62]  
Jakobisiak M, 2003, INT J ONCOL, V23, P1055
[63]   CELL CYCLE-SPECIFIC EFFECTS OF LOVASTATIN [J].
JAKOBISIAK, M ;
BRUNO, S ;
SKIERSKI, JS ;
DARZYNKIEWICZ, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3628-3632
[64]   Inhibition of pancreatic stellate cell activation by the hydroxymethylglutaryl coenzyme A reductase inhibitor lovastatin [J].
Jaster, R ;
Brock, P ;
Sparmann, G ;
Emmrich, J ;
Liebe, S .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (08) :1295-1303
[65]   Rapid improvement of nitric oxide bioavailability after lipid-lowering therapy with cerivastatin within two weeks [J].
John, S ;
Delles, C ;
Jacobi, J ;
Schlaich, MP ;
Schneider, M ;
Schmitz, G ;
Schmieder, RE .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (05) :1351-1358
[66]   Randomized phase II trial comparing bevacizumab plus carboplatin and paclitaxel with carboplatin and paclitaxel alone in previously untreated locally advanced or metastatic non-small-cell lung cancer [J].
Johnson, DH ;
Fehrenbacher, L ;
Novotny, WF ;
Herbst, RS ;
Nemunaitis, JJ ;
Jablons, DM ;
Langer, CJ ;
DeVore, RF ;
Gaudreault, J ;
Damico, LA ;
Holmgren, E ;
Kabbinavar, F .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (11) :2184-2191
[67]   Activation of VEGF and Ras genes in gastric mucosa during angiogenic response to ethanol injury [J].
Jones, MK ;
Itani, RM ;
Wang, HT ;
Tomikawa, M ;
Sarfeh, IJ ;
Szabo, S ;
Tarnawski, AS .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 276 (06) :G1345-G1355
[68]   Heme oxygenase and angiogenic activity of endothelial cells:: Stimulation by carbon monoxide and inhibition by tin protoporphyrin-IX [J].
Józkowicz, A ;
Huk, H ;
Nigisch, A ;
Weigel, G ;
Dietrich, W ;
Motterlini, R ;
Dulak, J .
ANTIOXIDANTS & REDOX SIGNALING, 2003, 5 (02) :155-162
[69]   All hydrophobic HMG-CoA reductase inhibitors induce apoptotic death in rat pulmonary vein endothelial cells [J].
Kaneta, S ;
Satoh, K ;
Kano, S ;
Kanda, M ;
Ichihara, K .
ATHEROSCLEROSIS, 2003, 170 (02) :237-243
[70]   Potential anticancer effects of statins: Fact or fiction? [J].
Kaushal, V ;
Kohli, M ;
Mehta, P ;
Mehta, JL .
ENDOTHELIUM-JOURNAL OF ENDOTHELIAL CELL RESEARCH, 2003, 10 (01) :49-58