Impaired oxygen-sensitive regulation of mitochondrial biogenesis within the von Hippel–Lindau syndrome
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C. Larsson | A. von Kriegsheim | R. Zubarev | O. Bedoya-Reina | Yihai Cao | M. Henriksson | J. Ruas | Javier Rodríguez | J. Holmberg | P. Jannig | Shuijie Li | Juan Yuan | P. Bullova | S. Schlisio | Jieyu Wu | Wenyu Li | C. Suzuki | A. Smed-Sörensen | Paula Valente-Silva | M. Plescher | Xuepei Zhang | Yong Liu | Meng Yu | C. Christofer Juhlin
[1] Laura E. Herring,et al. Genome-wide Screening Identifies SFMBT1 as an Oncogenic Driver in Cancer with VHL Loss. , 2020, Molecular cell.
[2] Laura E. Herring,et al. TBK1 is a Synthetic Lethal Target in Cancer with VHL Loss. , 2019, Cancer discovery.
[3] C. Larsson,et al. EglN3 hydroxylase stabilizes BIM-EL linking VHL type 2C mutations to pheochromocytoma pathogenesis and chemotherapy resistance , 2019, Proceedings of the National Academy of Sciences.
[4] C. Fan,et al. VHL substrate transcription factor ZHX2 as an oncogenic driver in clear cell renal cell carcinoma , 2018, Science.
[5] P. Cramer,et al. Structural Basis of Mitochondrial Transcription Initiation , 2017, Cell.
[6] O. Surova,et al. Neuroblast differentiation during development and in neuroblastoma requires KIF1Bβ-mediated transport of TRKA , 2017, Genes & development.
[7] Matthew G. Vander Heiden,et al. Understanding the Intersections between Metabolism and Cancer Biology , 2017, Cell.
[8] W. Kaelin. The VHL Tumor Suppressor Gene: Insights into Oxygen Sensing and Cancer. , 2017, Transactions of the American Clinical and Climatological Association.
[9] K. Gardner,et al. Targeting renal cell carcinoma with a HIF-2 antagonist , 2016, Nature.
[10] J. Cheng,et al. pVHL suppresses kinase activity of Akt in a proline-hydroxylation–dependent manner , 2016, Science.
[11] F. Gage,et al. Metabolic reprogramming during neuronal differentiation from aerobic glycolysis to neuronal oxidative phosphorylation , 2016, eLife.
[12] A. von Kriegsheim,et al. Substrate-Trapped Interactors of PHD3 and FIH Cluster in Distinct Signaling Pathways , 2016, Cell reports.
[13] U. Hellman,et al. The 1p36 Tumor Suppressor KIF 1Bβ Is Required for Calcineurin Activation, Controlling Mitochondrial Fission and Apoptosis. , 2016, Developmental cell.
[14] D. Figarella-Branger,et al. Somatic gain-of-function HIF2A mutations in sporadic central nervous system hemangioblastomas , 2016, Journal of Neuro-Oncology.
[15] Y. Xiong,et al. WT1 recruits TET2 to regulate its target gene expression and suppress leukemia cell proliferation. , 2015, Molecular cell.
[16] D. Lindgren,et al. Primary clear cell renal carcinoma cells display minimal mitochondrial respiratory capacity resulting in pronounced sensitivity to glycolytic inhibition by 3-Bromopyruvate , 2015, Cell Death and Disease.
[17] S. Richard,et al. Genetic evidence of a precisely tuned dysregulation in the hypoxia signaling pathway during oncogenesis. , 2014, Cancer research.
[18] Jenny Welander,et al. Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma. , 2014, The Journal of clinical endocrinology and metabolism.
[19] S. Srikantan,et al. In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas. , 2013, Endocrine-related cancer.
[20] D. Temiakov,et al. Phosphorylation of human TFAM in mitochondria impairs DNA binding and promotes degradation by the AAA+ Lon protease. , 2013, Molecular cell.
[21] Electron Kebebew,et al. Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia. , 2012, The New England journal of medicine.
[22] W. Harris,et al. Metabolic differentiation in the embryonic retina , 2012, Nature Cell Biology.
[23] J. Hornick,et al. Succinate Dehydrogenase-deficient Tumors: Diagnostic Advances and Clinical Implications , 2012, Advances in anatomic pathology.
[24] D. Gale,et al. Dysregulation of the HIF pathway due to VHL mutation causing severe erythrocytosis and pulmonary arterial hypertension. , 2011, Blood.
[25] Martijn A. Huynen,et al. TEFM (c17orf42) is necessary for transcription of human mtDNA , 2011, Nucleic acids research.
[26] Yuichi Matsushima,et al. Mitochondrial Lon protease regulates mitochondrial DNA copy number and transcription by selective degradation of mitochondrial transcription factor A (TFAM) , 2010, Proceedings of the National Academy of Sciences.
[27] Omar Abdel-Wahab,et al. The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate. , 2010, Cancer cell.
[28] Robert S. Freeman,et al. Oxygen-Regulated β2-Adrenergic Receptor Hydroxylation by EGLN3 and Ubiquitylation by pVHL , 2009, Science Signaling.
[29] W. Kaelin. The von Hippel–Lindau tumour suppressor protein: O2 sensing and cancer , 2008, Nature Reviews Cancer.
[30] Christoph Handschin,et al. The role of exercise and PGC1α in inflammation and chronic disease , 2008, Nature.
[31] W. Kaelin,et al. Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway. , 2008, Molecular cell.
[32] M. Meyerson,et al. The kinesin KIF1Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor. , 2008, Genes & development.
[33] S. Signoretti,et al. VHL loss actuates a HIF-independent senescence programme mediated by Rb and p400 , 2008, Nature Cell Biology.
[34] A. Pause,et al. Collagen matrix assembly is driven by the interaction of von Hippel–Lindau tumor suppressor protein with hydroxylated collagen IV alpha 2 , 2008, Oncogene.
[35] M. McMullin,et al. A gain-of-function mutation in the HIF2A gene in familial erythrocytosis. , 2008, The New England journal of medicine.
[36] W. Rathmell,et al. von Hippel-Lindau mutation in mice recapitulates Chuvash polycythemia via hypoxia-inducible factor-2alpha signaling and splenic erythropoiesis. , 2007, The Journal of clinical investigation.
[37] G. Semenza,et al. HIF-1 inhibits mitochondrial biogenesis and cellular respiration in VHL-deficient renal cell carcinoma by repression of C-MYC activity. , 2007, Cancer cell.
[38] P. Ratcliffe,et al. Interaction of Hydroxylated Collagen IV with the von Hippel-Lindau Tumor Suppressor* , 2007, Journal of Biological Chemistry.
[39] Kentaro Takahashi,et al. Von Hippel-Lindau Disease , 2024 .
[40] Huiyun Liang,et al. PGC-1alpha: a key regulator of energy metabolism. , 2006, Advances in physiology education.
[41] W. Kaelin,et al. Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer. , 2005, Cancer cell.
[42] P. Choyke,et al. Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors. , 2004, Blood.
[43] P. Choyke,et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. , 2003, American journal of human genetics.
[44] William Kim,et al. The von Hippel-Lindau tumor suppressor protein: new insights into oxygen sensing and cancer. , 2003, Current opinion in genetics & development.
[45] David Mole,et al. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia , 2002, Nature Genetics.
[46] P. Ratcliffe,et al. Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease. , 2001, Human molecular genetics.
[47] M. Ivan,et al. von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF. , 2001, Human molecular genetics.
[48] K. Nagashima,et al. The von Hippel-Lindau tumor suppressor targets to mitochondria. , 2000, Cancer research.
[49] T. Shuin,et al. Direct interaction of the beta-domain of VHL tumor suppressor protein with the regulatory domain of atypical PKC isotypes. , 1999, Biochemical and biophysical research communications.
[50] C. Wykoff,et al. The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis , 1999, Nature.
[51] D. Louis,et al. The von Hippel-Lindau tumor suppressor protein is required for proper assembly of an extracellular fibronectin matrix. , 1998, Molecular cell.
[52] H. Brauch,et al. Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene. , 1997, The Journal of clinical endocrinology and metabolism.
[53] LA Greene,et al. Nerve growth factor prevents the death and stimulates the neuronal differentiation of clonal PC12 pheochromocytoma cells in serum-free medium , 1978, The Journal of cell biology.
[54] L. Greene,et al. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. , 1976, Proceedings of the National Academy of Sciences of the United States of America.