Glucose catabolism in cancer cells: amplification of the gene encoding type II hexokinase.

Hexokinase type II is highly overexpressed in many cancer cells, where it plays a pivotal role in the high glycolytic phenotype. Here we demonstrate by Southern blot analysis and fluorescence in situ hybridization (FISH) that in the rapidly growing rat AS-30D hepatoma cell line, enhanced hexokinase activity is associated with at least a 5-fold amplification of the type II gene relative to normal hepatocytes. This amplification is located chromosomally, extends to the whole gene, and most likely occurs at the site of the resident gene. No rearrangement of the gene could be detected. Therefore, overexpression of hexokinase type II in AS-30D hepatoma cells may be based, at least in part, on a stable gene amplification. This is the first report describing the amplification of a hexokinase gene in a tumor cell line expressing the high glycolytic phenotype.

[1]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[2]  P. Pedersen,et al.  Purification and characterization of a bindable form of mitochondrial bound hexokinase from the highly glycolytic AS-30D rat hepatoma cell line. , 1988, Cancer research.

[3]  Hermona Soreq,et al.  Amplification, enhanced expression and possible rearrangement of EGF receptor gene in primary human brain tumours of glial origin , 1985, Nature.

[4]  T. Sugimura,et al.  Hexokinase isozyme patterns of human uterine tumors , 1972, Cancer.

[5]  A. Razin,et al.  DNA methylation and gene expression , 1991, Microbiological reviews.

[6]  D. Mayer,et al.  Differences in expression and intracellular distribution of hexokinase isoenzymes in rat liver cells of different transformation stages. , 1994, Biochimica et biophysica acta.

[7]  References , 1971 .

[8]  D. Frank Culture of Animal Cells: A Manual of Basic Technique , 1984, The Yale Journal of Biology and Medicine.

[9]  J. Wilson,et al.  Complete amino acid sequence of the type II isozyme of rat hexokinase, deduced from the cloned cDNA: comparison with a hexokinase from novikoff ascites tumor. , 1991, Archives of biochemistry and biophysics.

[10]  Saroj P. Mathupala,et al.  Glucose Catabolism in Cancer Cells. , 1995, The Journal of Biological Chemistry.

[11]  B. Nelson,et al.  Evidence that transcription of the hexokinase gene is increased in a rapidly growing rat hepatoma. , 1985, Biochemical and biophysical research communications.

[12]  P. Pedersen,et al.  Intracellular localization and properties of particulate hexokinase in the Novikoff ascites tumor. Evidence for an outer mitochondrial membrane location. , 1983, The Journal of biological chemistry.

[13]  H. Sather,et al.  Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. , 1985, The New England journal of medicine.

[14]  G Hermanson,et al.  High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. , 1990, Science.

[15]  J. Orenstein,et al.  Growth and structural properties of epithelial cell cultures established from normal rat liver and chemically induced hepatomas. , 1975, Cancer research.

[16]  P. Pedersen,et al.  Functional significance of mitochondrial bound hexokinase in tumor cell metabolism. Evidence for preferential phosphorylation of glucose by intramitochondrially generated ATP. , 1988, The Journal of biological chemistry.

[17]  F. Alt,et al.  Amplification and rearrangement of DNA sequences from the chromosomal region 2p24 in human neuroblastomas. , 1986, Cancer research.