1. Heat shock protein 90 inhibition and multi‐target approach to maximize cardioprotection in ischaemic injury
- Author
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H. Aceros, Nicolas Noiseux, M. Borie, Shant Der Sarkissian, Pierre-Marc Williams, and Catherine Scalabrini
- Subjects
0301 basic medicine ,Pharmacology ,Cardioprotection ,business.industry ,Optimal treatment ,Myocardial Ischemia ,Antineoplastic Agents ,Disease ,Hsp90 inhibitor ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Multi target ,Pharmacological interventions ,Heat shock protein ,Humans ,Medicine ,Ischaemic heart disease ,HSP90 Heat-Shock Proteins ,business ,Review Articles ,Neuroscience ,030217 neurology & neurosurgery - Abstract
Despite several advances in medicine, ischaemic heart disease remains a major cause of morbidity and mortality. The unravelling of molecular mechanisms underlying disease pathophysiology has revealed targets for pharmacological interventions. However, transfer of these pharmcological possibilities to clinical use has been disappointing. Considering the complexity of ischaemic disease at the cellular and molecular levels, an equally multifaceted treatment approach may be envisioned. The pharmacological principle of ‘one target, one key’ may fall short in such contexts, and optimal treatment may involve one or many agents directed against complementary targets. Here, we introduce a ‘multi‐target approach to cardioprotection’ and propose heat shock protein 90 (HSP90) as a target of interest. We report on a member of a distinct class of HSP90 inhibitor possessing pleiotropic activity, which we found to exhibit potent infarct‐sparing effects.
- Published
- 2020
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