Difference between revisions of "Samper 2009 Free Radic Biol Med"
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|authors=Samper E, Morgado L, Estrada JC, Bernad A, Hubbard A, Cadenas S, Melov S | |authors=Samper E, Morgado L, Estrada JC, Bernad A, Hubbard A, Cadenas S, Melov S | ||
|year=2009 | |year=2009 | ||
|journal=Free | |journal=Free Radic Biol Med | ||
|abstract=Lymphomas adapt to their environment by undergoing a complex series of biochemical changes that are | |abstract=Lymphomas adapt to their environment by undergoing a complex series of biochemical changes that are | ||
currently not well understood. To better define these changes, we examined the gene expression and gene | currently not well understood. To better define these changes, we examined the gene expression and gene | ||
| Line 22: | Line 22: | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|injuries=RONS; Oxidative Stress, Genetic Defect; Knockdown; Overexpression | |injuries=RONS; Oxidative Stress, Genetic Defect; Knockdown; Overexpression | ||
| | |couplingstates=OXPHOS, ETS | ||
|topics=Mitochondrial Biogenesis; Mitochondrial Density | |||
|discipline=Biomedicine | |discipline=Biomedicine | ||
}} | }} | ||
Revision as of 12:06, 17 August 2012
| Samper E, Morgado L, Estrada JC, Bernad A, Hubbard A, Cadenas S, Melov S (2009) Increase in mitochondrial biogenesis, oxidative stress, and glycolysis in murine lymphomas. Free Radic Biol Med 46: 387-396. |
Samper E, Morgado L, Estrada JC, Bernad A, Hubbard A, Cadenas S, Melov S (2009) Free Radic Biol Med
Abstract: Lymphomas adapt to their environment by undergoing a complex series of biochemical changes that are currently not well understood. To better define these changes, we examined the gene expression and gene ontology profiles of thymic lymphomas from a commonly used model of carcinogenesis, the p53−/− mouse. These tumors show a highly significant upregulation of mitochondrial biogenesis, mitochondrial protein translation, mtDNA copy number, reactive oxygen species, antioxidant defenses, proton transport, ATP synthesis, hypoxia response, and glycolysis, indicating a fundamental change in the bioenergetic profile of the transformed T cell. Our results suggest that T cell tumorigenesis involves a simultaneous upregulation of mitochondrial biogenesis, mitochondrial respiration, and glycolytic activity. These processes would allow cells to adapt to the stressful tumor environment by facilitating energy production and thereby promote tumor growth. Understanding these adaptations is likely to result in improved therapeutic strategies for this tumor type. • Keywords: Mitochondria, Reactive oxygen species, Glycolysis, Lymphoma, p53, c-myc, Free radicals
Labels:
Stress:RONS; Oxidative Stress"RONS; Oxidative Stress" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property., Genetic Defect; Knockdown; Overexpression"Genetic Defect; Knockdown; Overexpression" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property.
Regulation: Mitochondrial Biogenesis; Mitochondrial Density"Mitochondrial Biogenesis; Mitochondrial Density" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property.
Coupling state: OXPHOS, ETS"ETS" is not in the list (LEAK, ROUTINE, OXPHOS, ET) of allowed values for the "Coupling states" property.
HRR: Oxygraph-2k
