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Spotlight on the relevance of mtDNA in cancer
Cruz-Bermúdez, A; Vicente-Blanco, RJ; Gonzalez-Vioque, E; Provencio, M; Fernández-Moreno, MA; Garesse, R.
Afiliação
  • Cruz-Bermúdez, A; University Autonomus Madrid. Facultad de Medicina. Departamento de Bioquímica. Madrid. Spain
  • Vicente-Blanco, RJ; University Autonomus Madrid. Facultad de Medicina. Departamento de Bioquímica. Majadahonda. Spain
  • Gonzalez-Vioque, E; Hospital Universitario Puerta de Hierro-Majadahonda. Servicio de Bioquímica. Madrid. Spain
  • Provencio, M; Hospital Universitario Puerta de Hierro-Majadahonda. Servicio de Oncología Médica. Madrid. Spain
  • Fernández-Moreno, MA; University Autonomus Madrid. Facultad de Medicina. Departamento de Bioquímica. Madrid. Spain
  • Garesse, R; University Autonomus Madrid. Facultad de Medicina. Departamento de Bioquímic. Madrid. Spain
Clin. transl. oncol. (Print) ; 19(4): 409-418, abr. 2017. tab, ilus
Article em En | IBECS | ID: ibc-160889
Biblioteca responsável: ES1.1
Localização: BNCS
ABSTRACT
The potential role of the mitochondrial genome has recently attracted interest because of its high mutation frequency in tumors. Different aspects of mtDNA make it relevant for cancer‘s biology, such as it encodes a limited but essential number of genes for OXPHOS biogenesis, it is particularly susceptible to mutations, and its copy number can vary. Moreover, most ROS in mitochondria are produced by the electron transport chain. These characteristics place the mtDNA in the center of multiple signaling pathways, known as mitochondrial retrograde signaling, which modifies numerous key processes in cancer. Cybrid studies support that mtDNA mutations are relevant and exert their effect through a modification of OXPHOS function and ROS production. However, there is still much controversy regarding the clinical relevance of mtDNA mutations. New studies should focus more on OXPHOS dysfunction associated with a specific mutational signature rather than the presence of mutations in the mtDNA (AU)
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Coleções: 06-national / ES Base de dados: IBECS Assunto principal: Fosforilação Oxidativa / DNA Mitocondrial / Espécies Reativas de Oxigênio / Neoplasias Limite: Female / Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Article
Buscar no Google
Coleções: 06-national / ES Base de dados: IBECS Assunto principal: Fosforilação Oxidativa / DNA Mitocondrial / Espécies Reativas de Oxigênio / Neoplasias Limite: Female / Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Article