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TIGAR, a p53-Inducible Regulator of Glycolysis and Apoptosis

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TLDR
expression of TIGAR may modulate the apoptotic response to p53, allowing survival in the face of mild or transient stress signals that may be reversed or repaired, and the decrease of intracellular ROS levels in response to TIGar may also play a role in the ability of p53 to protect from the accumulation of genomic damage.
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This article is published in Cell.The article was published on 2006-07-14 and is currently open access. It has received 1803 citations till now. The article focuses on the topics: TP53-inducible glycolysis and apoptosis regulator & Apoptosis Regulator.

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The Warburg effect in tumor progression: Mitochondrial oxidative metabolism as an anti-metastasis mechanism

TL;DR: The findings reveal mitochondrial oxidative metabolism as a critical suppressor of metastasis and justify metabolic therapies for potential prevention/intervention of tumor metastasis.
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Coping with stress: multiple ways to activate p53

Henning F. Horn, +1 more
- 26 Feb 2007 - 
TL;DR: This review will highlight some recently identified roles for p53 in tumour suppression, and discuss some of the numerous mechanisms through which p53 can be regulated and activated.
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Glucose-6-phosphate dehydrogenase, NADPH, and cell survival

TL;DR: It is now clear that G6PD is under complex regulatory control and of central importance to many cellular processes.
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Phosphofructokinase 1 Glycosylation Regulates Cell Growth and Metabolism

TL;DR: It is demonstrated that the dynamic posttranslational modification of proteins by O-linked β-N-acetylglucosamine (O-GlcNAcylation) is a key metabolic regulator of glucose metabolism and was induced at serine 529 of phosphofructokinase 1 (PFK1) in response to hypoxia.
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p53 post-translational modification: deregulated in tumorigenesis

TL;DR: The recent advances in understanding of the wide spectrum of post-translational modifications that act as epigenetic-like codes for modulating specific functions of p53 in vivo are reviewed and how deregulation of these modifications might contribute to tumorigenesis are reviewed.
References
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Journal ArticleDOI

On the origin of cancer cells.

Origin of cancer cells

Otto Warburg
Journal ArticleDOI

Surfing the p53 network

TL;DR: The p53 tumour-suppressor gene integrates numerous signals that control cell life and death, and the disruption of p53 has severe consequences when a highly connected node in the Internet breaks down.
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In vivo activation of the p53 pathway by small-molecule antagonists of MDM2.

TL;DR: In this article, the authors identify potent and selective small-molecule antagonists of MDM2 and confirm their mode of action through the crystal structures of complexes, leading to cell cycle arrest, apoptosis, and growth inhibition of human tumor xenografts.
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Live or let die: the cell's response to p53

TL;DR: Understanding the complex mechanisms that regulate whether or not a cell dies in response to p53 will ultimately contribute to the development of therapeutic strategies to repair the apoptotic p53 response in cancers.
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