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      Omics-based approaches to understand mechanosensitive endothelial biology and atherosclerosis : Omics-based approaches in atherosclerosis

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          Abstract

          <p class="first" id="P1">Atherosclerosis is a multifactorial disease that preferentially occurs in arterial regions exposed to disturbed blood flow (d-flow). The mechanisms by which d-flow induces atherosclerosis involve changes in the transcriptome, methylome, proteome, and metabolome of multiple vascular cells, especially endothelial cells. Initially, we begin with the pathogenesis of atherosclerosis and the changes that occur at multiple levels owing to d-flow, especially in the endothelium. Also, there are a variety of strategies used for the global profiling of the genome, transcriptome, miRNA-nome, DNA methylome, and metabolome that are important to define the biological and pathophysiological mechanisms of endothelial dysfunction and atherosclerosis. Finally, systems biology can be used to integrate these ‘omics’ datasets, especially those that derive data based on a single animal model, in order to better understand the pathophysiology of atherosclerosis development in a holistic manner and how this integrative approach could be used to identify novel molecular diagnostics and therapeutic targets to prevent or treat atherosclerosis. </p>

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          Author and article information

          Journal
          Wiley Interdisciplinary Reviews: Systems Biology and Medicine
          WIREs Syst Biol Med
          Wiley
          19395094
          September 2016
          September 2016
          June 24 2016
          : 8
          : 5
          : 378-401
          Affiliations
          [1 ]The Wallace H. Coulter Department of Biomedical Engineering; Georgia Institute of Technology; Atlanta GA USA
          Article
          10.1002/wsbm.1344
          4983228
          27341633
          3d15c3a8-a3b5-40f1-806f-824997e21f1e
          © 2016

          http://doi.wiley.com/10.1002/tdm_license_1.1

          http://onlinelibrary.wiley.com/termsAndConditions#vor

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