Histone Deacetylase (HDAC) Inhibition as a Novel Treatment for Diabetes Mellitus

Molecular medicine (Cambridge, Mass.)(2011)

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摘要
Both common forms of diabetes have an inflammatory pathogenesis in which immune and metabolic factors converge on interleukin-1β as a key mediator of insulin resistance and β-cell failure. In addition to improving insulin resistance and preventing β-cell inflammatory damage, there is evidence of genetic association between diabetes and histone deacetylases (HDACs); and HDAC inhibitors (HDACi) promote β-cell development, proliferation, differentiation and function and positively affect late diabetic microvascular complications. Here we review this evidence and propose that there is a strong rationale for preclinical studies and clinical trials with the aim of testing the utility of HDACi as a novel therapy for diabetes.
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关键词
HDAC Inhibitors (HDACi),Pancreatic And Duodenal Homeobox 1 (PDX1),C/EBP Homologous Protein (CHOP),HDACi Treatment,Suberoylanilide Hydroxamic Acid (SAHA)
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