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A Proteomics Approach to Investigate miR-153-3p and miR-205-5p Targets in Neuroblastoma Cells.
Patil, Ketan S; Basak, Indranil; Pal, Ramavati; Ho, Hsin-Pin; Alves, Guido; Chang, Emmanuel J; Larsen, Jan Petter; Møller, Simon Geir.
Afiliación
  • Patil KS; Department of Biological Sciences, St. John's University, New York, NY, 11439, United States of America.
  • Basak I; Department of Biological Sciences, St. John's University, New York, NY, 11439, United States of America.
  • Pal R; Department of Biological Sciences, St. John's University, New York, NY, 11439, United States of America.
  • Ho HP; Department of Chemistry, York College and the Graduate Center, The City University of New York, New York, NY, 11451, United States of America.
  • Alves G; Norwegian Center for Movement Disorders, Stavanger University Hospital, 4068, Stavanger, Norway.
  • Chang EJ; Department of Chemistry, York College and the Graduate Center, The City University of New York, New York, NY, 11451, United States of America.
  • Larsen JP; Norwegian Center for Movement Disorders, Stavanger University Hospital, 4068, Stavanger, Norway.
  • Møller SG; Department of Biological Sciences, St. John's University, New York, NY, 11439, United States of America.
PLoS One ; 10(12): e0143969, 2015.
Article en En | MEDLINE | ID: mdl-26633009
MicroRNAs are key regulators associated with numerous diseases. In HEK293 cells, miR-153-3p and miR-205-5p down-regulate alpha-synuclein (SNCA) and Leucine-rich repeat kinase 2 (LRRK2), two key proteins involved in Parkinson's disease (PD). We have used two-dimensional gel electrophoresis (2D-PAGE) coupled to mass spectrometry (MS) to identify a spectrum of miR-153-3p and miR-205-5p targets in neuronal SH-SY5Y cells. We overexpressed and inhibited both microRNAs in SH-SY5Y cells and through comparative proteomics profiling we quantified ~240 protein spots from each analysis. Combined, thirty-three protein spots were identified showing significant (p-value < 0.05) changes in abundance. Modulation of miR-153-3p resulted in seven up-regulated proteins and eight down-regulated proteins. miR-205 modulation resulted in twelve up-regulated proteins and six down-regulated proteins. Several of the proteins are associated with neuronal processes, including peroxiredoxin-2 and -4, cofilin-1, prefoldin 2, alpha-enolase, human nucleoside diphosphate kinase B (Nm23) and 14-3-3 protein epsilon. Many of the differentially expressed proteins are involved in diverse pathways including metabolism, neurotrophin signaling, actin cytoskeletal regulation, HIF-1 signaling and the proteasome indicating that miR-153-3p and miR-205-5p are involved in the regulation of a wide variety of biological processes in neuroblastoma cells.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: MicroARNs / Proteómica / Proteínas de Neoplasias / Neuroblastoma Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: MicroARNs / Proteómica / Proteínas de Neoplasias / Neuroblastoma Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos