Statins inhibit HMG-CoA reductase by competitively inhibiting the active site of the enzyme, thus preventing cholesterol synthesis and reducing the risk of developing cardiovascular disease. Many pleiotropic effects of statins have been demonstrated that can be either related or unrelated to their cholesterol-lowering ability. Among these effects are their proangiogenic and antiangiogenic properties that could offer new therapeutic applications. In this regard, pro- and anti-angiogenic properties of statins have been shown to be dose dependent. Statins also appear to have a variety of non-cardiovascular angiogenic effects in many diseases, some examples being ocular disease, brain disease, cancer, preeclampsia, diabetes and bone disease, which are discussed in this review using reports from in vitro and in vivo investigations.

Zahedipour, F., Butler, A.E., Rizzo, M., Sahebkar, A. (2022). Statins and angiogenesis in non-cardiovascular diseases [10.1016/j.drudis.2022.07.005].

Statins and angiogenesis in non-cardiovascular diseases

Rizzo, Manfredi;
2022-10-01

Abstract

Statins inhibit HMG-CoA reductase by competitively inhibiting the active site of the enzyme, thus preventing cholesterol synthesis and reducing the risk of developing cardiovascular disease. Many pleiotropic effects of statins have been demonstrated that can be either related or unrelated to their cholesterol-lowering ability. Among these effects are their proangiogenic and antiangiogenic properties that could offer new therapeutic applications. In this regard, pro- and anti-angiogenic properties of statins have been shown to be dose dependent. Statins also appear to have a variety of non-cardiovascular angiogenic effects in many diseases, some examples being ocular disease, brain disease, cancer, preeclampsia, diabetes and bone disease, which are discussed in this review using reports from in vitro and in vivo investigations.
ott-2022
Zahedipour, F., Butler, A.E., Rizzo, M., Sahebkar, A. (2022). Statins and angiogenesis in non-cardiovascular diseases [10.1016/j.drudis.2022.07.005].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/584549
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