An inducible gene product for 6-phosphofructo-2-kinase with an AU-rich instability element: Role in tumor cell glycolysis and the Warburg effect
Open Access
- 16 March 1999
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 96 (6) , 3047-3052
- https://doi.org/10.1073/pnas.96.6.3047
Abstract
Cancer cells maintain a high glycolytic rate even in the presence of oxygen, a phenomenon first described over 70 years ago and known historically as the Warburg effect. Fructose 2,6-bisphosphate is a powerful allosteric regulator of glycolysis that acts to stimulate the activity of 6-phosphofructo-1-kinase (PFK-1), the most important control point in mammalian glycolysis. The steady state concentration of fructose 2,6-bisphosphate in turn depends on the activity of the enzyme 6-phosphofructo-2-kinase (PFK-2)/fructose-2,6-bisphosphatase, which is expressed in several tissue-specific isoforms. We report herein the identification of a gene product for this enzyme that is induced by proinflammatory stimuli and which is distinguished by the presence of multiple copies of the AUUUA mRNA instability motif in its 3′-untranslated end. This inducible gene for PFK-2 is expressed constitutively in several human cancer cell lines and was found to be required for tumor cell growth in vitro and in vivo. Inhibition of inducible PFK-2 protein expression decreased the intracellular level of 5-phosphoribosyl-1-pyrophosphate, a product of the pentose phosphate pathway and an important precursor for nucleic acid biosynthesis. These studies identify a regulatory isoenzyme that may be essential for tumor growth and provide an explanation for long-standing observations concerning the apparent coupling of enhanced glycolysis and cell proliferation.Keywords
This publication has 26 references indexed in Scilit:
- Fructose 2,6-bisphosphate metabolism in Ehrlich ascites tumour cellsZeitschrift für Krebsforschung und Klinische Onkologie, 1995
- Fructose 2,6-bisphosphate and the control of glycolysis by growth factors, tumor promoters and oncogenesAdvances in Enzyme Regulation, 1993
- Inhibition of 6-phosphofructo-2-kinase activity by mercaptopurinesBiochemical Pharmacology, 1992
- PRIMARY RESPONSE GENES INDUCED BY GROWTH FACTORS AND TUMOR PROMOTERSAnnual Review of Biochemistry, 1991
- The impairment of respiration by glycolysis in the Lewis lung carcinomaCancer Letters, 1990
- A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradationCell, 1986
- Posttranscriptional mechanisms are responsible for accumulation of truncated c-myc RNAs in murine plasma cell tumorsCell, 1985
- Glycolysis—one of the keys to cancer?Trends in Pharmacological Sciences, 1980
- Enzymology of Cancer CellsNew England Journal of Medicine, 1977
- On the Origin of Cancer CellsScience, 1956