Evidence map›Paper›PMID 8700847›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

Expression of the fructose transporter GLUT5 in human breast cancer.

S P Zamora-León, D W Golde, I I Concha, C I Rivas, F Delgado-López, J Baselga, F Nualart, J C Vera

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

78 citing papers in PubMed, 210 citations in OpenAlex.

  1. Review
  2. Conformational changes in ketohexokinase are conserved across isozymes and species.Acta crystallographica. Section F, Structural biology communications · 2025
    Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. GLUT5-overexpression-related tumorigenic implications.Molecular medicine (Cambridge, Mass.) · 2024
    Review
  9. Review
  10. Review
  11. Fructose metabolism is unregulated in cancers and placentae.Experimental biology and medicine (Maywood, N.J.) · 2024
    Review
  12. Review
  13. Article
  14. GLUT5: structure, functions, diseases and potential applications.Acta biochimica et biophysica Sinica · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

S P Zamora-LeónProgram in Molecular Pharmacology and Therapeutics, Memorial Sloan-Kettering Cancer Center, NY 10021, USA.
D W Golde
I I Concha
C I Rivas
F Delgado-López
J Baselga
F Nualart
J C Vera
University of Concepción · CLMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
HUMORAL REGULATION OF NORMAL AND MALIGNANT HEMOPOIESISR01CA030388 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KELLY, THOMAS J · 1985 to 2004
$1.9M
HEMATOPOIETIC CELL FUNCTION IN AIDSR01HL042107 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOLDE, DAVID W · 1988 to 1999
–
HUMORAL REGULATION OF NORMAL AND MALIGNANT HEMPOIESISR37CA030388 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOLDE, DAVID W · 1986 to 1993
–
NCI NIH HHS CA30388NCI NIH HHS P30 CA08748NHLBI NIH HHS R01 HL42107
6 · The paper itself

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.

Indexed as

BreastBreast NeoplasmsDeoxyglucoseEpitheliumFructoseGlucose Transporter Type 1Glucose Transporter Type 2Glucose Transporter Type 5HumansImmunologic TechniquesMonosaccharide Transport ProteinsTumor Cells, CulturedDeoxyglucoseFructoseGlucose Transporter Type 1Glucose Transporter Type 2Glucose Transporter Type 5Monosaccharide Transport ProteinsSLC2A1 protein, human

Identifiers

PMID8700847
PMCPMC39870
OpenAlexW2097687227

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.