Journal Article

Inorganic Polyphosphate Stimulates Mammalian TOR, a Kinase Involved in the Proliferation of Mammary Cancer Cells

Roth, Richard A., Fraley, Cresson D., Kornberg, Arthur, Wang, Lihong, Faridi, Jesika

2003

Overview

Inorganic polyphosphate (poly P), chains of hundreds of phosphate residues linked by \"high-energy\" bonds as in ATP, has been conserved from prebiotic times in all cells. Poly P is essential for a wide variety of functions in bacteria, including virulence in pathogens. In this study, we observe the unique and many-fold stimulation by poly P in vitro of the protein kinase mTOR (mammalian target of rapamycin). To explore the role of poly P in mammalian cells, a yeast polyphosphatase, PPX1, was inserted into the chromosomes of MCF-7 mammary cancer cells. The transfected cells are markedly deficient in their response to mitogens, such as insulin and amino acids, as seen in their failure to activate mTOR to phosphorylate one of its substrates, PHAS-I (the initiation factor 4E-binding protein). In addition, the transfected cells are severely reduced in their growth in a serum-free medium. On the basis of these findings, we suggest that poly P (and/or PPX1) serves as a regulatory factor in the activation of mTOR in the proliferative signaling pathways of animal cells.

• Publisher: National Academy of Sciences,National Acad Sciences
• Subject: Amino acids / Animal cells / Base Sequence / Biochemistry / Biological Sciences / Breast Neoplasms - enzymology / Breast Neoplasms - pathology / Cancer / Cell Division - physiology / Cell growth / Cell lines / Cells / Chromosomes / DNA Primers / Enzyme Activation / Enzymes / Humans / Insulin / Mammals / Phosphates / Phosphates - pharmacology / Phosphorylation / Plasmids / Polyphosphates / Protein Kinase Inhibitors / Protein Kinases - metabolism / Protein Kinases - physiology / Proteins / TOR Serine-Threonine Kinases / Tumor Cells, Cultured / Yeasts