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PLoS One ; 10(8): e0133512, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26244761

RESUMO

Histone deacetylases (HDAC's) became increasingly important targets for therapy of various diseases, resulting in a pressing need to develop HDAC class- and isoform-selective inhibitors. Class IIa deacetylases possess only minimal deacetylase activity against acetylated histones, but have several other client proteins as substrates through which they participate in epigenetic regulation. Herein, we report the radiosyntheses of the second generation of HDAC class IIa-specific radiotracers: 6-(di-fluoroacetamido)-1-hexanoicanilide (DFAHA) and 6-(tri-fluoroacetamido)-1-hexanoicanilide ([18F]-TFAHA). The selectivity of these radiotracer substrates to HDAC class IIa enzymes was assessed in vitro, in a panel of recombinant HDACs, and in vivo using PET/CT imaging in rats. [18F]TFAHA showed significantly higher selectivity for HDAC class IIa enzymes, as compared to [18F]DFAHA and previously reported [18F]FAHA. PET imaging with [18F]TFAHA can be used to visualize and quantify spatial distribution and magnitude of HDAC class IIa expression-activity in different organs and tissues in vivo. Furthermore, PET imaging with [18F]TFAHA may advance the understanding of HDACs class IIa mediated epigenetic regulation of normal and pathophysiological processes, and facilitate the development of novel HDAC class IIa-specific inhibitors for therapy of different diseases.


Assuntos
Encéfalo/diagnóstico por imagem , Encéfalo/metabolismo , Diagnóstico por Imagem/métodos , Epigênese Genética , Histona Desacetilases/metabolismo , Traçadores Radioativos , Animais , Autorradiografia , Radioisótopos de Flúor/metabolismo , Tomografia por Emissão de Pósitrons/métodos , Ratos Sprague-Dawley , Reprodutibilidade dos Testes , Especificidade por Substrato , Tomografia Computadorizada por Raios X/métodos
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