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PMID: 8700847 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expression of the fructose transporter GLUT5 in human breast cancer.

Zamora-León SP, Golde DW, Concha II, Rivas CI, Delgado-López F, Baselga J, Nualart F, Vera JC

Abstract

The primary metabolic characteristic of malignant cells is an increased uptake of glucose and its anaerobic metabolism. We studied the expression and function of the glucose transporters in human breast cancer cell lines and analyzed their expression in normal and neoplastic primary human breast tissue. Hexose uptake assays and immunoblotting experiments revealed that the breast carcinoma cell lines MCF-7 and MDA-468 express the glucose transporters GLUT1 and GLUT2, isoforms expressed in both normal and neoplastic breast tissue. We also found that the breast cancer cell lines transport fructose and express the fructose transporter GLUT5. Immunolocalization studies revealed that GLUT5 is highly expressed in vivo in human breast cancer but is absent in normal human breast tissue. These findings indicate that human breast cancer cells have a specialized capacity to transport fructose, a metabolic substrate believed to be used by few human tissues. Identification of a high-affinity fructose transporter on human breast cancer cells opens opportunities to develop novel strategies for early diagnosis and treatment of breast cancer.

MeSH Terms
Breast/metabolism Breast Neoplasms/metabolism Deoxyglucose/metabolism Epithelium/metabolism Fructose/metabolism Glucose Transporter Type 1 Glucose Transporter Type 2 Glucose Transporter Type 5 Humans Immunologic Techniques Monosaccharide Transport Proteins/immunology,metabolism Tumor Cells, Cultured
Chemicals
Glucose Transporter Type 1 Glucose Transporter Type 2 Glucose Transporter Type 5 Monosaccharide Transport Proteins SLC2A1 protein, human Fructose Deoxyglucose
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Zamora-León S P
Program in Molecular Pharmacology and Therapeutics, Memorial Sloan-Kettering Cancer Center, NY 10021, USA.
Golde D W
Concha I I
Rivas C I
Delgado-López F
Baselga J
Nualart F
Vera J C
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1996-03-05
Pages
1847-52
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC39870
Subset
IM
Grants
NCI NIH HHS · CA30388 · United States
NCI NIH HHS · P30 CA08748 · United States
NHLBI NIH HHS · R01 HL42107 · United States
Corrections
ErratumIn
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