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      Impact of microRNAs on ischemic stroke: From pre- to post-disease.

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          Abstract

          Stroke is the number one cause of neurological dysfunction in adults and has a heavy socioeconomic burden worldwide. The etiological origins of ischemic stroke and resulting pathological processes are mediated by a multifaceted cascade of molecular mechanisms that are in part modulated by posttranscriptional activity. Accumulating evidence has revealed a role for microRNAs (miRNAs) as essential mediators of posttranscriptional gene silencing in both the physiology of brain development and pathology of ischemic stroke. In this review, we compile miRNAs that have been reported to regulate various stroke risk factors and pre-disease mechanisms, including hypertension, atherosclerosis, and diabetes, followed by an in-depth analysis of miRNAs in ischemic stroke pathogenesis, such as excitotoxicity, oxidative stress, inflammation, apoptosis, angiogenesis and neurogenesis. Since promoting or suppressing expression of miRNAs by specific pharmaceutical and non-pharmaceutical therapies may be beneficial to post-stroke recovery, we also highlight the potential therapeutic value of miRNAs in clinical settings.

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          Author and article information

          Journal
          Prog. Neurobiol.
          Progress in neurobiology
          Elsevier BV
          1873-5118
          0301-0082
          Aug 24 2017
          Affiliations
          [1 ] Cerebrovascular Diseases Research Institute and Department of Neurology, Xuanwu Hospital of Capital Medical University, Beijing 10053, China.
          [2 ] Department of Neurological Surgery, University of Wisconsin, Madison, WI, USA.
          [3 ] Department of Neurological Surgery, University of Wisconsin, Madison, WI, USA; Cellular and Molecular Pathology Graduate Program, University of Wisconsin, Madison, WI, USA.
          [4 ] Department of Neurology, University of Pittsburgh School of Medicine, PA, USA.
          [5 ] Department of Neurological Surgery, University of Wisconsin, Madison, WI, USA; Cellular and Molecular Pathology Graduate Program, University of Wisconsin, Madison, WI, USA; William S. Middleton VA Hospital, Madison, WI, USA. Electronic address: vemuganti@neurosurgery.wisc.edu.
          [6 ] Cerebrovascular Diseases Research Institute and Department of Neurology, Xuanwu Hospital of Capital Medical University, Beijing 10053, China; Beijing Institute for Brain Disorders and Beijing Key Laboratory of Translational Medicine for Cerebrovascular Diseases, Beijing 10053, China. Electronic address: yumin111@ccmu.edu.cn.
          Article
          S0301-0082(17)30033-3
          10.1016/j.pneurobio.2017.08.002
          28842356
          b2a86a3d-81c5-491a-8e9d-401c08cd5ef4
          History

          Atherosclerosis,Diabetes,Hypertension,Stroke,microRNAs
          Atherosclerosis, Diabetes, Hypertension, Stroke, microRNAs

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