Evidence map›Paper›PMID 25093285›Full record

ReviewBiochemical pharmacology2014

Heterogeneity of glycolysis in cancers and therapeutic opportunities.

Marc O Warmoes, Jason W Locasale

Abstract readReview
In one paragraph

Review in Biochemical pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Review
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  9. Review
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  11. Article
  12. Metabolic barriers to cancer immunotherapy.Nature reviews. Immunology · 2021
    Review
  13. Article
  14. Article
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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

2 authors.

Marc O WarmoesDivision of Nutritional Sciences, Cornell University, Ithaca, NY, United States.
Jason W LocasaleDivision of Nutritional Sciences, Cornell University, Ithaca, NY, United States. Electronic address: locasale@cornell.edu.

Funding

The developmental layers in the CD8+ T cell response to chronic infectionR01AI110613 · NIAID · CORNELL UNIVERSITY · PI GRIMSON, ANDREW W, RUDD, BRIAN DAVID · 2014 to 2022
$4.1M
Understanding metabolic flux and the control of mammalian cell growthR00CA168997 · NCI · DUKE UNIVERSITY · PI LOCASALE, JASON W. · 2013 to 2015
$695k
NCI NIH HHS R00 CA168997NCI NIH HHS R00CA168997NIAID NIH HHS 401 R01AI110613NIAID NIH HHS R01 AI110613
6 · The paper itself

Abstract

Upregulated glycolysis, both in normoxic and hypoxic environments, is a nearly universal trait of cancer cells. The enormous difference in glucose metabolism offers a target for therapeutic intervention with a potentially low toxicity profile. The past decade has seen a steep rise in the development and clinical assessment of small molecules that target glycolysis. The enzymes in glycolysis have a highly heterogeneous nature that allows for the different bioenergetic, biosynthetic, and signaling demands needed for various tissue functions. In cancers, these properties enable them to respond to the variable requirements of cell survival, proliferation and adaptation to nutrient availability. Heterogeneity in glycolysis occurs through the expression of different isoforms, posttranslational modifications that affect the kinetic and regulatory properties of the enzyme. In this review, we will explore this vast heterogeneity of glycolysis and discuss how this information might be exploited to better target glucose metabolism and offer possibilities for biomarker development.

Indexed as

BiomarkersEnergy MetabolismGlucoseGlycolysisHumansNeoplasmsOxygen ConsumptionPhosphotransferasesUp-RegulationBiomarkersGlucosePhosphotransferases2-deoxyglucose (PubChem CID: 9062)3-PO (PubChem CID: 5720233)Anti-glycolytic agentsBromopyruvate (PubChem CID: 70684)CancerGlycolysisIsoenzymesPGMI-004A (PubChem CID: 66521681)SpliceformsTEP-46 (Chem CID: 44246499)

Identifiers

PMID25093285
PMCPMC4254151

What OpenQuestion holds

Textmetadata
LicenceTDM
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.