The interaction among glucose transport, hexokinase, and glucose-6-phosphatase with respect to 3H-2-deoxyglucose retention in murine tumor models

Nucl Med Biol. 1996 May;23(4):533-41. doi: 10.1016/0969-8051(96)00037-6.

Abstract

The development of new diagnostic/therapeutic modalities for cancer requires a specific understanding of how tumors differ from normal tissues. Though the key components involved in the selective accumulation of 2-deoxy-D-glucose (2-DG) analogs in tumors are known, the relative importance of each is controversial. For this reason glucose transport protein (GLUT) density, hexokinase/glucose-6-phosphatase (GP) activity, and 2-DG biodistribution were measured together in four tumor models and normal murine tissues. Direct binding studies with 3H-cytochalasin B showed that GLUT density was elevated 20-fold in LX-1 tumors. Immunohistochemically in all tumors, the expression of GLUT-1 was highest in the necrotic/ perinecrotic foci and similar in cells not adjacent to necrotic foci. As the retention of 3H-2-DG was similar in all tumors, these data suggest that the GLUT-1 in perinecrotic tumor cells were not rate limiting for 3H-2-DG uptake. Kidney, liver, and lung had high GP activity and rapid clearance of 3H-2-DG. Sodium orthovanadate (5 mumol), a GP inhibitor, increased the concentration of 3H-2-DG in these tissues, suggesting that GP is a rate-limiting enzyme for 3H-2-DG clearance. All tumor homogenates had low GP activity, and hexokinase activity was not elevated compared to normal tissues. Thus, in the tumors studied, the selective accumulation of 3H-2-DG consistently occurred in the absence of significant GP activity without the marked overexpression of hexokinase or GLUT.

MeSH terms

  • Animals
  • Antimetabolites / pharmacokinetics*
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Deoxyglucose / pharmacokinetics*
  • Female
  • Glucose-6-Phosphatase / antagonists & inhibitors
  • Glucose-6-Phosphatase / metabolism*
  • Hexokinase / metabolism*
  • Humans
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / pathology
  • Mice
  • Mice, Nude
  • Monosaccharide Transport Proteins / metabolism*
  • Necrosis
  • Neoplasm Transplantation
  • Tissue Distribution
  • Transplantation, Heterologous
  • Tritium

Substances

  • Antimetabolites
  • Monosaccharide Transport Proteins
  • Tritium
  • Deoxyglucose
  • Hexokinase
  • Glucose-6-Phosphatase