Oxidation of alpha-ketoglutarate is required for reductive carboxylation in cancer cells with mitochondrial defects.
暂无分享,去创建一个
R. Deberardinis | W. Linehan | D. Rakheja | Lucas B. Sullivan | N. Chandel | W. Linehan | Xiaolei Shi | A. Mullen | Zeping Hu | Lei Jiang | Lindsey K. Boroughs | Z. Kovács | R. Boriack
[1] C. Moraes,et al. An out‐of‐frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production , 2000, Annals of neurology.
[2] J. Weinberg,et al. Mitochondrial dysfunction during hypoxia/reoxygenation and its correction by anaerobic metabolism of citric acid cycle intermediates. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[3] P. W. Hochachka,et al. Multiple end products of anaerobiosis in diving vertebrates. , 1975, Comparative biochemistry and physiology. B, Comparative biochemistry.
[4] R. Deberardinis,et al. Analysis of tumor metabolism reveals mitochondrial glucose oxidation in genetically diverse human glioblastomas in the mouse brain in vivo. , 2012, Cell metabolism.
[5] Thomas M. Wasylenko,et al. Reductive glutamine metabolism is a function of the α-ketoglutarate to citrate ratio in cells , 2013, Nature Communications.
[6] B. Devlin,et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. , 2000, Science.
[7] P. W. Hochachka,et al. Metabolic consequences of diving in animals and man. , 1975, Science.
[8] P. Meltzer,et al. Succinate dehydrogenase mutation underlies global epigenomic divergence in gastrointestinal stromal tumor. , 2013, Cancer discovery.
[9] F. H. van der Westhuizen,et al. Metabolomics of urinary organic acids in respiratory chain deficiencies in children , 2011, Metabolomics.
[10] E S Husebye,et al. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. , 2001, American journal of human genetics.
[11] Ralph J Deberardinis,et al. Brick by brick: metabolism and tumor cell growth. , 2008, Current opinion in genetics & development.
[12] G. Stephanopoulos,et al. Cofactor Balance by Nicotinamide Nucleotide Transhydrogenase (NNT) Coordinates Reductive Carboxylation and Glucose Catabolism in the Tricarboxylic Acid (TCA) Cycle*♦ , 2013, The Journal of Biological Chemistry.
[13] L. Cantley,et al. Breathless cancer cells get fat on glutamine , 2012, Cell Research.
[14] Laurent Poulain,et al. Understanding the central role of citrate in the metabolism of cancer cells. , 2012, Biochimica et biophysica acta.
[15] C. Ludwig,et al. A Role for Cytosolic Fumarate Hydratase in Urea Cycle Metabolism and Renal Neoplasia , 2013, Cell reports.
[16] E. Schaftingen,et al. l-2-Hydroxyglutaric aciduria, a defect of metabolite repair , 2007, Journal of Inherited Metabolic Disease.
[17] C. Rock,et al. Cancer-associated Isocitrate Dehydrogenase Mutations Inactivate NADPH-dependent Reductive Carboxylation* , 2012, The Journal of Biological Chemistry.
[18] R. Deberardinis,et al. Isocitrate dehydrogenase 1/2 mutational analyses and 2‐hydroxyglutarate measurements in Wilms tumors , 2011, Pediatric blood & cancer.
[19] D. Rakheja,et al. Papillary thyroid carcinoma shows elevated levels of 2-hydroxyglutarate , 2011, Tumor Biology.
[20] Karsten Hiller,et al. Profiling metabolic networks to study cancer metabolism. , 2013, Current opinion in biotechnology.
[21] Christian M. Metallo,et al. Reductive glutamine metabolism by IDH1 mediates lipogenesis under hypoxia , 2011, Nature.
[22] H. Esumi,et al. The NADH‐fumarate reductase system, a novel mitochondrial energy metabolism, is a new target for anticancer therapy in tumor microenvironments , 2010, Annals of the New York Academy of Sciences.
[23] W. Marston Linehan,et al. Reductive carboxylation supports growth in tumor cells with defective mitochondria , 2011, Nature.
[24] L. Sazanov,et al. Proton‐translocating transhydrogenase and NAD‐ and NADP‐linked isocitrate dehydrogenases operate in a substrate cycle which contributes to fine regulation of the tricarboxylic acid cycle activity in mitochondria , 1994, FEBS letters.
[25] W. Wheaton,et al. Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity , 2010, Proceedings of the National Academy of Sciences.
[26] T. Shlomi,et al. Fatty Acid Labeling from Glutamine in Hypoxia Can Be Explained by Isotope Exchange without Net Reductive Isocitrate Dehydrogenase (IDH) Flux , 2013, The Journal of Biological Chemistry.
[27] Gabriela Kalna,et al. Haem oxygenase is synthetically lethal with the tumour suppressor fumarate hydratase , 2011, Nature.
[28] G. Stephanopoulos,et al. In vivo HIF-mediated reductive carboxylation is regulated by citrate levels and sensitizes VHL-deficient cells to glutamine deprivation. , 2013, Cell metabolism.
[29] A. Paetau,et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer , 2002, Nature Genetics.
[30] W. Kaelin,et al. Influence of Metabolism on Epigenetics and Disease , 2013, Cell.
[31] R. Deberardinis,et al. Pyruvate carboxylase is required for glutamine-independent growth of tumor cells , 2011, Proceedings of the National Academy of Sciences.
[32] L. Liau,et al. Cancer-associated IDH1 mutations produce 2-hydroxyglutarate , 2009, Nature.
[33] T. Fan,et al. Altered regulation of metabolic pathways in human lung cancer discerned by 13C stable isotope-resolved metabolomics (SIRM) , 2009, Molecular Cancer.
[34] T. Yagi,et al. Mitochondrial complex I activity and NAD+/NADH balance regulate breast cancer progression. , 2013, The Journal of clinical investigation.
[35] Ulrich Müller,et al. Mutations in SDHC cause autosomal dominant paraganglioma, type 3 , 2000, Nature Genetics.
[36] T. Soga,et al. Inhibition of Mitochondrial Aconitase by Succination in Fumarate Hydratase Deficiency , 2013, Cell reports.
[37] K. Clarke,et al. Dysregulation of hypoxia pathways in fumarate hydratase-deficient cells is independent of defective mitochondrial metabolism. , 2010, Human molecular genetics.
[38] Jesse M. Platt,et al. Hypoxia promotes isocitrate dehydrogenase-dependent carboxylation of α-ketoglutarate to citrate to support cell growth and viability , 2011, Proceedings of the National Academy of Sciences.