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Connecting Neuronal Cell Protective Pathways and Drug Combinations in a Huntington's Disease Model through the Application of Quantitative Systems Pharmacology.
Pei, Fen; Li, Hongchun; Henderson, Mark J; Titus, Steven A; Jadhav, Ajit; Simeonov, Anton; Cobanoglu, Murat Can; Mousavi, Seyed H; Shun, Tongying; McDermott, Lee; Iyer, Prema; Fioravanti, Michael; Carlisle, Diane; Friedlander, Robert M; Bahar, Ivet; Taylor, D Lansing; Lezon, Timothy R; Stern, Andrew M; Schurdak, Mark E.
Afiliación
  • Pei F; Department of Computational and Systems Biology, University of Pittsburgh, 3501 Fifth Ave, Suite 3064, Biomedical Science Tower 3, Pittsburgh, PA, 15260, USA.
  • Li H; Department of Computational and Systems Biology, University of Pittsburgh, 3501 Fifth Ave, Suite 3064, Biomedical Science Tower 3, Pittsburgh, PA, 15260, USA.
  • Henderson MJ; National Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, MD, 20850, USA.
  • Titus SA; National Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, MD, 20850, USA.
  • Jadhav A; National Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, MD, 20850, USA.
  • Simeonov A; National Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, MD, 20850, USA.
  • Cobanoglu MC; Department of Computational and Systems Biology, University of Pittsburgh, 3501 Fifth Ave, Suite 3064, Biomedical Science Tower 3, Pittsburgh, PA, 15260, USA.
  • Mousavi SH; Department of Neurological Surgery, University of Pittsburgh, 200 Lothrop St., UPMC Presbyterian, Suite B-400, Pittsburgh, PA, 15261, USA.
  • Shun T; University of Pittsburgh Drug Discovery Institute, 200 Lothrop St., W950 Biomedical Science Tower Pittsburgh, PA, 15261, USA.
  • McDermott L; Department of Pharmaceutical Sciences, University of Pittsburgh, 3501 Terrace St., Pittsburgh, PA, 15261, USA.
  • Iyer P; Department of Pharmaceutical Sciences, University of Pittsburgh, 3501 Terrace St., Pittsburgh, PA, 15261, USA.
  • Fioravanti M; Department of Pharmaceutical Sciences, University of Pittsburgh, 3501 Terrace St., Pittsburgh, PA, 15261, USA.
  • Carlisle D; Department of Neurological Surgery, University of Pittsburgh, 200 Lothrop St., UPMC Presbyterian, Suite B-400, Pittsburgh, PA, 15261, USA.
  • Friedlander RM; Department of Neurological Surgery, University of Pittsburgh, 200 Lothrop St., UPMC Presbyterian, Suite B-400, Pittsburgh, PA, 15261, USA.
  • Bahar I; University of Pittsburgh Brain Institute, 3501 Fifth Ave., 4074 Biomedical Science Tower 3, Pittsburgh, PA, 15261, USA.
  • Taylor DL; Department of Computational and Systems Biology, University of Pittsburgh, 3501 Fifth Ave, Suite 3064, Biomedical Science Tower 3, Pittsburgh, PA, 15260, USA.
  • Lezon TR; University of Pittsburgh Drug Discovery Institute, 200 Lothrop St., W950 Biomedical Science Tower Pittsburgh, PA, 15261, USA.
  • Stern AM; Department of Computational and Systems Biology, University of Pittsburgh, 3501 Fifth Ave, Suite 3064, Biomedical Science Tower 3, Pittsburgh, PA, 15260, USA.
  • Schurdak ME; University of Pittsburgh Drug Discovery Institute, 200 Lothrop St., W950 Biomedical Science Tower Pittsburgh, PA, 15261, USA.
Sci Rep ; 7(1): 17803, 2017 12 19.
Article en En | MEDLINE | ID: mdl-29259176
ABSTRACT
Quantitative Systems Pharmacology (QSP) is a drug discovery approach that integrates computational and experimental methods in an iterative way to gain a comprehensive, unbiased understanding of disease processes to inform effective therapeutic strategies. We report the implementation of QSP to Huntington's Disease, with the application of a chemogenomics platform to identify strategies to protect neuronal cells from mutant huntingtin induced death. Using the STHdh Q111 cell model, we investigated the protective effects of small molecule probes having diverse canonical modes-of-action to infer pathways of neuronal cell protection connected to drug mechanism. Several mechanistically diverse protective probes were identified, most of which showed less than 50% efficacy. Specific combinations of these probes were synergistic in enhancing efficacy. Computational analysis of these probes revealed a convergence of pathways indicating activation of PKA. Analysis of phospho-PKA levels showed lower cytoplasmic levels in STHdh Q111 cells compared to wild type STHdh Q7 cells, and these levels were increased by several of the protective compounds. Pharmacological inhibition of PKA activity reduced protection supporting the hypothesis that protection may be working, in part, through activation of the PKA network. The systems-level studies described here can be broadly applied to any discovery strategy involving small molecule modulation of disease phenotype.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Huntington / Sustancias Protectoras / Neuronas Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Huntington / Sustancias Protectoras / Neuronas Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos
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