Evidence map›Paper›PMID 27648352›Full record

ReviewAmerican journal of cancer research2016

Glucose transport: meeting the metabolic demands of cancer, and applications in glioblastoma treatment.

Collin M Labak, Paul Y Wang, Rishab Arora, Maheedhara R Guda, Swapna Asuthkar, Andrew J Tsung, Kiran K Velpula

Open access · greenAbstract readReview
In one paragraph

Review in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Single-ligand dual-targeting lipid nanoparticles for therapeutic mRNA delivery to glioblastoma across the blood-brain barrier.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. PIM1 kinase and its diverse substrate in solid tumors.Cell communication and signaling : CCS · 2024
    Review
  10. Article
  11. Article
  12. Glioblastoma Therapy: Past, Present and Future.International journal of molecular sciences · 2024
    Review
  13. Engineering metabolism to modulate immunity.Advanced drug delivery reviews · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Glioblastoma Metabolism: Insights and Therapeutic Strategies.International journal of molecular sciences · 2023
    Review
  18. Ion Channels in Gliomas-From Molecular Basis to Treatment.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Collin M LabakDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria Peoria, IL, USA.
Paul Y WangDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria Peoria, IL, USA.
Rishab AroraDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria Peoria, IL, USA.
Maheedhara R GudaDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria Peoria, IL, USA.
Swapna AsuthkarDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria Peoria, IL, USA.
Andrew J TsungDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at PeoriaPeoria, IL, USA; Department of Neurosurgery, University of Illinois College of Medicine at PeoriaPeoria, IL, USA; Department of Illinois Neurological InstitutePeoria, IL, USA.
Kiran K VelpulaDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at PeoriaPeoria, IL, USA; Department of Neurosurgery, University of Illinois College of Medicine at PeoriaPeoria, IL, USA; Department of Microbiology, Yogi Vemana UniversityKadapa, India.
Illinois College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GLUT1, and to a lesser extent, GLUT3, appear to be interesting targets in the treatment of glioblastoma multiforme. The current review aims to give a brief history of the scientific community's understanding of these glucose transporters and to relate their importance to the metabolic changes that occur as a result of cancer. One of the primary changes that occurs in cancer, the Warburg Effect, is characterized by an extreme shift toward glycolysis from the usual reliance on oxidative phosphorylation and is currently being investigated to target the upstream and downstream factors responsible for Warburg-induced changes. Further, it aims to explain the differential expression of GLUT1 and GLUT3 in glioblastoma tissue, and how these modulations in expression can serve as targets to restore a more normal metabolism. Additionally, hypoxia-induced factor-1α's (HIF1α) role in a number of transcriptional changes typical to GBM will be discussed, including its role in GLUT upregulation. Finally, the four known subtypes of GBM [proneural, neural, mesenchymal, and classical] will be characterized in order to discuss how metabolic changes differ in each subtype. These changes have the potential to be selectively targeted in order to provide specificity to the clinical treatment options in GBM.

Indexed as

glioblastomaGLUT1GLUT3hypoxiaWarburg effect

Identifiers

PMID27648352
PMCPMC5004066
OpenAlexW2538639834

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.