Redox regulation of metabolic and signaling pathways by thioredoxin and glutaredoxin in NOS-3 overexpressing hepatoblastoma cells》.pdf
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Redox regulation of metabolic and signaling pathways by thioredoxin and glutaredoxin in NOS-3 overexpressing hepatoblastoma cells》.pdf
Redox Biology 6 (2015) 122–134
Contents lists available at ScienceDirect
Redox Biology
journal homepage: /locate/redox
Research Paper
Redox regulation of metabolic and signaling pathways by thioredoxin
and glutaredoxin in NOS-3 overexpressing hepatoblastoma cells
Raúl González a,b,n, M. José López-Grueso a, Jordi Muntané c,d, J. Antonio Bárcena a,b,
C. Alicia Padilla a,b
a Departamento de Bioquímica y Biología Molecular, Universidad de Córdoba, Córdoba, Spain
b Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain
c Departamento de Cirugía General, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS)/CSIC/Universidad de Sevilla, Sevilla,
Spain
d Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Spain
a r t i c l e i n f o a b s t r a c t
Article history: Nitric oxide (NO) plays relevant roles in signal transduction in physiopathology and its effects are de-
Received 22 May 2015 pendent on several environmental factors. NO has both pro-apoptotic and anti-apoptotic functions but
Received in revised form the molecular mechanisms responsible for these opposite effects are not fully understood. The action of
9 July 2015 NO occurs mainly through redox changes in target proteins, particularly by S-nitrosylation of reactive
Accepted 14 July 2015
cysteine residues. Thioredoxin (Trx) and glutaredoxin (Grx) systems
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