Overexpression of glut‐1 glucose transporter in human breast cancer an immunohistochemical study

Raya S. Brown, Richard L. Wahl

Research output: Contribution to journalArticlepeer-review

485 Scopus citations


Background. Breast cancers have higher than normal glucose metabolism, but the mechanism of glucose entry into these tumors is not well understood. Methods. The expression of five facilitative glucose transporters, Glut‐1 (erythrocyte type), Glut‐2 (liver type), Glut‐3 (brain type), Glut‐4 (muscle/fat type), and Glut‐5 (small intestine type), was studied by immunohistochemistry of paraffin sections from 12 primary human breast cancers and 8 lymph node metastases from 2 patients. Rat tissues known to express these glucose transporters were used as controls. Results. All the primary breast cancers and the lymph node metastases were positive for Glut‐1. This transporter was expressed on the cell membrane and in the cytoplasm of the tumor cells, but exhibited marked intratumoral and intertumoral variability in the proportions of positive cells and the intensity of staining. Staining of the normal mammary epithelium, if present, was much lower than observed in tumor cells from the same patient. Glut‐2 was expressed in all of the tumors, but the intensity of staining was not consistently stronger than that seen in healthy breast. Clusters of Glut‐4‐positive granule were observed in cells in six of the tumors. None of the tumors or the healthy breast in the tissues studied expressed Glut‐3 or Glut‐5. Conclusions. Higher expression of the glucose transporter Glut‐1 by breast cancer cells compared with the healthy breast tissue is common. Increased glucose transporter protein expression may contribute to the increased uptake of 2‐[18F]‐fluoro‐2‐deoxy‐D‐glucose (FDG) by these tumors observed by positron emission tomography (PET) imaging.

Original languageEnglish (US)
Pages (from-to)2979-2985
Number of pages7
Issue number10
StatePublished - Nov 15 1993
Externally publishedYes


  • breast cancer
  • glucose transporters
  • immunohistochemistry
  • tumor marker

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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