| Literature DB >> 32927022 |
Mazaher Ahmadi1, Shayan Amiri2, Stevan Pecic3, Filip Machaj4, Jakub Rosik4, Marek J Łos5, Javad Alizadeh6, Reza Mahdian7, Simone C da Silva Rosa8, Dedmer Schaafsma9, Shahla Shojaei10, Tayyebeh Madrakian1, Amir A Zeki11, Saeid Ghavami12.
Abstract
The statin drugs ('statins') potently inhibit hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase by competitively blocking the active site of the enzyme. Statins decrease de novo cholesterol biosynthesis and thereby reduce plasma cholesterol levels. Statins exhibit "pleiotropic" properties that are independent of their lipid-lowering effects. For example, preclinical evidence suggests that statins inhibit tumor growth and induce apoptosis in specific cancer cell types. Furthermore, statins show chemo-sensitizing effects by impairing Ras family GTPase signaling. However, whether statins have clinically meaningful anti-cancer effects remains an area of active investigation. Both preclinical and clinical studies on the potential mechanisms of action of statins in several cancers have been reviewed in the literature. Considering the contradictory data on their efficacy, we present an up-to-date summary of the pleiotropic effects of statins in cancer therapy and review their impact on different malignancies. We also discuss the synergistic anti-cancer effects of statins when combined with other more conventional anti-cancer drugs to highlight areas of potential therapeutic development.Entities:
Keywords: Apoptosis; Autophagy; Cancer therapy; Chemotherapy; Mevalonate cascade; Prenylation
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Year: 2020 PMID: 32927022 DOI: 10.1016/j.bbadis.2020.165968
Source DB: PubMed Journal: Biochim Biophys Acta Mol Basis Dis ISSN: 0925-4439 Impact factor: 5.187