Hypoxia, HIF1 and glucose metabolism in the solid tumour
By N. Denko. Nature Reviews. Cancer, 2008
1,650 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/084cab7ee20efc335d903465b85ca42f6f863d39
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In Cancer Research
In Molecular Biology
Citations in the corpus
- Metabolic Modulation of Glioblastoma with Dichloroacetate (2010, background): “Although we studied mROS (mitochondrial superoxide), controversy exists whether HIF-1a activation in cancer is associated with an overall increase or decrease in ROS [reviewed in (28)].”
- The LKB1-AMPK pathway: metabolism and growth control in tumor suppression (2009, background): “Well-established HIF1 transcriptional targets that contain hypoxia-responsive elements in their promoters include angiogenic factors, such as vascular endothelial growth factor A ( VEGFA ) and angiopoetin 2 ( ANG2 ), several glycolytic enzymes and multiple members of the glucose transporter (GLUT) f”
- Hooked on fat: the role of lipid synthesis in cancer metabolism and tumour development (2013, background): “…of HIF induces a number of metabolic Disease Models & Mechanisms 1359 The role of lipid synthesis in cancer REVIEW D ise as e M od el s & M ec ha ni sm s D M M alterations, most notably the induction of glycolysis and the inhibition of mitochondrial oxidative phosphorylation (Denko, 2008).”
- Probiotics modulated gut microbiota suppresses hepatocellular carcinoma growth in mice (2016, background): “Because HIF-1 could induce high level of GLUT-1 under hypoxia conditions (17), the aforementioned higher level of GLUT-1 (Fig.”
- Regulation of pyruvate metabolism and human disease (2013, background): “In regards to pyruvate metabolism, HIF1 regulates factors involved in glycolysis as well as PDK1, MCT4, and LDHA [150, 151].”
- Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity (2010, methodology): “de Coo, University Medical Center, Rotterdam, Netherlands) were previously described and were cultured in DMEM supplemented with 100 μg/ml uridine and 1 mM pyruvate (4).”
- The Lin28/let-7 axis regulates glucose metabolism (2011, background): “Reprogramming toward glyco- lytic metabolism can increase a cancer cell’s ability to generate biomass, a phenomenon termed the ‘‘Warburg Effect’’ (Denko, 2008; Engelman et al., 2006; Gao et al., 2009; Guertin and Sabatini, 2007; Laplante and Sabatini, 2009; Vander Heiden et al., 2009; Yun et al., 20”