Evidence map›Paper›PMID 26583064›Full record

ReviewOxidative medicine and cellular longevity2015

Key Roles of Glutamine Pathways in Reprogramming the Cancer Metabolism.

Krzysztof Piotr Michalak, Agnieszka Maćkowska-Kędziora, Bogusław Sobolewski, Piotr Woźniak

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

39 citing papers in PubMed, 87 citations in OpenAlex.

  1. Review
  2. Targeting the Glutaminolysis Pathway in Glaucoma-Associated Fibrosis.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

4 authors at 3 institutions in 1 country.

Krzysztof Piotr MichalakLaboratory of Vision Science and Optometry, Faculty of Physics, Adam Mickiewicz University of Poznań, Umultowska Street 85, 61-614 Poznań, Poland ; Nanobiomedical Center of Poznań, Umultowska Street 85, 61-614 Poznań, Poland.
Agnieszka Maćkowska-KędzioraDepartment of Clinical Pharmacology, Chair of Cardiology, Poznań University of Medical Sciences, Długa Street 1/2, 61-848 Poznań, Poland.
Bogusław SobolewskiPolish Mother's Memorial Hospital-Research Institute, Outpatient Clinic, Rzgowska Street 281/289, Łódź, Poland.
Piotr WoźniakPolish Mother's Memorial Hospital-Research Institute, Outpatient Clinic, Rzgowska Street 281/289, Łódź, Poland.
Polish Mother’s Memorial Hospital Research Institute · PLAdam Mickiewicz University in Poznań · PLPoznan University of Medical Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glutamine (GLN) is commonly known as an important metabolite used for the growth of cancer cells but the effects of its intake in cancer patients are still not clear. However, GLN is the main substrate for DNA and fatty acid synthesis. On the other hand, it reduces the oxidative stress by glutathione synthesis stimulation, stops the process of cancer cachexia, and nourishes the immunological system and the intestine epithelium, as well. The current paper deals with possible positive effects of GLN supplementation and conditions that should be fulfilled to obtain these effects. The analysis of GLN metabolism suggests that the separation of GLN and carbohydrates in the diet can minimize simultaneous supply of ATP (from glucose) and NADPH2 (from glutamine) to cancer cells. It should support to a larger extent the organism to fight against the cancer rather than the cancer cells. GLN cannot be considered the effective source of ATP for cancers with the impaired oxidative phosphorylation and pyruvate dehydrogenase inhibition. GLN intake restores decreased levels of glutathione in the case of chemotherapy and radiotherapy; thus, it facilitates regeneration processes of the intestine epithelium and immunological system.

Indexed as

GlioblastomaGluconeogenesisGlutamineGlutathioneHumansHypoxia-Inducible Factor 1, alpha SubunitKetone OxidoreductasesNeoplasmsReactive Oxygen SpeciesGlutamineGlutathioneHypoxia-Inducible Factor 1, alpha SubunitKetone Oxidoreductasespyruvate dehydrogenase (NADP+)Reactive Oxygen Species

Identifiers

PMID26583064
PMCPMC4637129
OpenAlexW2155319744

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.