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A comprehensive p75 neurotrophin receptor gene network and pathway analyses identifying new target genes.
Sajanti, Antti; Lyne, Seán B; Girard, Romuald; Frantzén, Janek; Rantamäki, Tomi; Heino, Iiro; Cao, Ying; Diniz, Cassiano; Umemori, Juzoh; Li, Yan; Takala, Riikka; Posti, Jussi P; Roine, Susanna; Koskimäki, Fredrika; Rahi, Melissa; Rinne, Jaakko; Castrén, Eero; Koskimäki, Janne.
Afiliação
  • Sajanti A; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Lyne SB; Neurovascular Surgery Program, Section of Neurosurgery, The University of Chicago Medicine and Biological Sciences, 5841 S. Maryland, Chicago, IL, 60637, USA.
  • Girard R; Neurovascular Surgery Program, Section of Neurosurgery, The University of Chicago Medicine and Biological Sciences, 5841 S. Maryland, Chicago, IL, 60637, USA.
  • Frantzén J; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Rantamäki T; Laboratory of Neurotherapeutics, Molecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences and Drug Research Program, Division of Pharmacology and Pharmacotherapy, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.
  • Heino I; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Cao Y; Neurovascular Surgery Program, Section of Neurosurgery, The University of Chicago Medicine and Biological Sciences, 5841 S. Maryland, Chicago, IL, 60637, USA.
  • Diniz C; Neuroscience Center, HiLIFE, University of Helsinki, Box 63, 00014, Helsinki, Finland.
  • Umemori J; Neuroscience Center, HiLIFE, University of Helsinki, Box 63, 00014, Helsinki, Finland.
  • Li Y; Neurovascular Surgery Program, Section of Neurosurgery, The University of Chicago Medicine and Biological Sciences, 5841 S. Maryland, Chicago, IL, 60637, USA.
  • Takala R; Center for Research Informatics, The University of Chicago, Chicago, IL, USA.
  • Posti JP; Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital, POB 52, 20521, Turku, Finland.
  • Roine S; Department of Anaesthesiology and Intensive Care, University of Turku, Turku, Finland.
  • Koskimäki F; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Rahi M; Division of Clinical Neurosciences, Department of Cerebrovascular Diseases, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Rinne J; Division of Clinical Neurosciences, Department of Cerebrovascular Diseases, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Castrén E; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
  • Koskimäki J; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Hämeentie 11, P.O. Box 52, 20521, Turku, Finland.
Sci Rep ; 10(1): 14984, 2020 09 11.
Article em En | MEDLINE | ID: mdl-32917932
ABSTRACT
P75 neurotrophic receptor (p75NTR) is an important receptor for the role of neurotrophins in modulating brain plasticity and apoptosis. The current understanding of the role of p75NTR in cellular adaptation following pathological insults remains blurred, which makes p75NTR's related signaling networks an interesting and challenging initial point of investigation. We identified p75NTR and related genes through extensive data mining of a PubMed literature search including published works related to p75NTR from the past 20 years. Bioinformatic network and pathway analyses of identified genes (n = 235) were performed using ReactomeFIViz in Cytoscape based on the highly reliable Reactome functional interaction network algorithm. This approach merges interactions extracted from human curated pathways with predicted interactions from machine learning. Genome-wide pathway analysis showed total of 16 enriched hierarchical clusters. A total of 278 enriched single pathways were also identified (p < 0.05, false discovery rate corrected). Gene network analyses showed multiple known and new targets in the p75NTR gene network. This study provides a comprehensive analysis and investigation into the current knowledge of p75NTR signaling networks and pathways. These results also identify several genes and their respective protein products as involved in the p75NTR network, which have not previously been clearly studied in this pathway. These results can be used to generate novel hypotheses to gain a greater understanding of p75NTR in acute brain injuries, neurodegenerative diseases and general response to cellular damage.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Lesões Encefálicas / Transdução de Sinais / Receptores de Fator de Crescimento Neural / Doenças Neurodegenerativas / Redes e Vias Metabólicas / Redes Reguladoras de Genes / Mineração de Dados / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Lesões Encefálicas / Transdução de Sinais / Receptores de Fator de Crescimento Neural / Doenças Neurodegenerativas / Redes e Vias Metabólicas / Redes Reguladoras de Genes / Mineração de Dados / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2020 Tipo de documento: Article