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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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Spatial reorganization of Saccharomyces cerevisiae enolase to alter carbon metabolism under hypoxia.

TL;DR: The results suggest that under hypoxia, S. cerevisiae cells sense mitochondrial ROS and, by the involvement of SNF1/AMPK, spatially reorganize metabolic enzymes in the cytosol via de novo protein synthesis, which subsequently increases carbon metabolism.
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Uncoupling the Warburg effect from cancer

TL;DR: Recent work by Salvador Moncada's group published in PNAS and other recent work from the same group provides exciting evidence supporting the idea that the Warburg effect is also required for the proliferation of noncancer cells.
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Is p53 Involved in Tissue-Specific Insulin Resistance Formation?

TL;DR: A profound insight is provided into p53-dependent metabolic actions directed towards promotion of insulin resistance as well as presenting experimental data regarding obesity-induced p 53-mediated metabolic abnormalities.
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p53 downregulates the gene expression of mitochondrial aconitase in human prostate carcinoma cells

TL;DR: Investigation of whether p53 regulates mACON expression and the potential mechanisms responsible for its effect on prostate cancer cells investigate the role of p53 in suppressing prostatic tumorigenesis.
References
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Journal ArticleDOI

On the origin of cancer cells.

Origin of cancer cells

Otto Warburg
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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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