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February 12, 2002Circulation684 citationsOpen Access

Statins Have Biphasic Effects on Angiogenesis

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MWMichael WeisCHChristopher HeeschenAGAlec Glassford

Key Result

Statins enhanced angiogenesis at low concentrations (0.005-0.01 micromol/L) but inhibited it at high concentrations (0.05-1 micromol/L) in vitro and in murine models.

Key Points

  • This research aims to investigate the dual effects of statins on angiogenesis under varying concentrations.
  • In vitro and in vivo experiments assessing endothelial cell behavior at different statin concentrations.
  • Murine models used to evaluate the impact of cerivastatin and atorvastatin on inflammation-induced angiogenesis.
  • Analyzed effects on vascular endothelial growth factor release and endothelial apoptosis.
  • Low-dose statins (0.005-0.01 micromol/L) enhanced endothelial cell proliferation and migration.
  • High-dose statins (0.05-1 micromol/L) significantly inhibited angiogenesis, reducing vascular endothelial growth factor release and increasing endothelial apoptosis.
  • In murine models, low-dose statins promoted angiogenesis, while high doses reduced tumor growth and vascularization.

Structured PICO

Do statins have a dose-dependent effect on angiogenesis in preclinical models?

P
Population
In vitro endothelial cells and in vivo murine models (inflammation-induced angiogenesis model, hyperlipidemic apolipoprotein E-deficient mice, and murine Lewis lung cancer model)
I
Intervention
Cerivastatin and atorvastatin at low concentrations (0.005 to 0.01 micromol/L in vitro; 0.5 mg/kg/d in vivo) and high concentrations (0.05 to 1 micromol/L in vitro; 2.5 mg/kg/d in vivo)
C
Comparator
Control/baseline and comparison between low and high doses
O
Outcome
Angiogenesis (endothelial cell proliferation, migration, and differentiation in vitro; vascularization in vivo)surrogate

Statins exhibit a biphasic, dose-dependent effect on angiogenesis, promoting it at low doses and inhibiting it at high doses via lipid-independent mechanisms.

Abstract

BACKGROUND: Statins inhibit HMG-CoA reductase to reduce the synthesis of cholesterol and isoprenoids that modulate diverse cell functions. We investigated the effect of the statins cerivastatin and atorvastatin on angiogenesis in vitro and in vivo. METHODS AND RESULTS: Endothelial cell proliferation, migration, and differentiation were enhanced at low concentrations (0.005 to 0.01 micromol/L) but significantly inhibited at high statin concentrations (0.05 to 1 micromol/L). Antiangiogenic effects at high concentrations were associated with decreased endothelial release of vascular endothelial growth factor and increased endothelial apoptosis and were reversed by geranylgeranyl pyrophosphate. In murine models, inflammation-induced angiogenesis was enhanced with low-dose statin therapy (0.5 mg x kg(-1) x d(-1)) but significantly inhibited with high concentrations of cerivastatin or atorvastatin (2.5 mg x kg(-1) x d(-1)). Despite the fact that high-dose statin treatment was effective at reducing lipid levels in hyperlipidemic apolipoprotein E-deficient mice, it impaired rather than enhanced angiogenesis. Finally, high-dose cerivastatin decreased tumor growth and tumor vascularization in a murine Lewis lung cancer model. CONCLUSIONS: HMG-CoA reductase inhibition has a biphasic dose-dependent effect on angiogenesis that is lipid independent and associated with alterations in endothelial apoptosis and vascular endothelial growth factor signaling. Statins have proangiogenic effects at low therapeutic concentrations but angiostatic effects at high concentrations that are reversed by geranylgeranyl pyrophosphate. At clinically relevant doses, statins may modulate angiogenesis in humans via effects on geranylated proteins.

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Cite This Study

Weis et al. (2002) studied this question. Statins (cerivastatin and atorvastatin) was evaluated on Angiogenesis (endothelial cell proliferation, migration, and differentiation). Statins enhanced angiogenesis at low concentrations (0.005-0.01 micromol/L) but inhibited it at high concentrations (0.05-1 micromol/L) in vitro and in murine models.

synapsesocial.com/papers/6a4c43a61ca1d7ad2a60e84ahttps://doi.org/10.1161/hc0602.103393
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