Evidence map›Paper›PMID 32812866›Full record

ArticleeLife2020

Metabolic but not transcriptional regulation by PKM2 is important for natural killer cell responses.

Jessica F Walls, Jeff J Subleski, Erika M Palmieri, Marieli Gonzalez-Cotto, Clair M Gardiner, Daniel W McVicar, David K Finlay

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

30 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Effect of PKM2 onFrontiers in cellular and infection microbiology · 2026
    Article
  6. Article
  7. Review
  8. Article
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  12. Article
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  14. Article
  15. Article
  16. Review
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  18. Role of Pyruvate Kinase M2 (PKM2) in Cardiovascular Diseases.Journal of cardiovascular translational research · 2023
    Review
  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

7 authors at 2 institutions in 2 countries.

Jessica F WallsSchool of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.ORCID 0000-0003-2901-3318
Jeff J SubleskiLaboratory of Cancer Immunometabolism, National Cancer Institute, Frederick, United States.
Erika M PalmieriLaboratory of Cancer Immunometabolism, National Cancer Institute, Frederick, United States.ORCID 0000-0002-4237-5324
Marieli Gonzalez-CottoLaboratory of Cancer Immunometabolism, National Cancer Institute, Frederick, United States.ORCID 0000-0003-3359-8814
Clair M Gardiner *School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Daniel W McVicar *Laboratory of Cancer Immunometabolism, National Cancer Institute, Frederick, United States.
David K Finlay *School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.ORCID 0000-0003-2716-6679
National Cancer Institute · USTrinity College Dublin · IE

Funding

Science Foundation Ireland 18/ERCS/6005Wellcome 106811/Z/15/ZWellcome Trust
6 · The paper itself

Abstract

Natural Killer (NK) cells have an important role in immune responses to viruses and tumours. Integrating changes in signal transduction pathways and cellular metabolism is essential for effective NK cells responses. The glycolytic enzyme Pyruvate Kinase Muscle 2 (PKM2) has described roles in regulating glycolytic flux and signal transduction, particularly gene transcription. While PKM2 expression is robustly induced in activated NK cells, mice lacking PKM2 in NK cells showed no defect in NK cell metabolism, transcription or antiviral responses to MCMV infection. NK cell metabolism was maintained due to compensatory PKM1 expression in PKM2-null NK cells. To further investigate the role of PKM2, we used TEPP-46, which increases PKM2 catalytic activity while inhibiting any PKM2 signalling functions. NK cells activated with TEPP-46 had reduced effector function due to TEPP-46-induced increases in oxidative stress. Overall, PKM2-regulated glycolytic metabolism and redox status, not transcriptional control, facilitate optimal NK cells responses.

Indexed as

Gene Expression RegulationGlycolysisPyruvate KinaseAnimalsCells, CulturedKiller Cells, NaturalMiceOxidative StressPyridazinesPyrrolesSignal TransductionML-265Pkm protein, mousePyridazinesPyrrolesPyruvate Kinasecell biologyimmunologyinflammationmetabolismmousenk cells

Identifiers

PMID32812866
PMCPMC7467725
OpenAlexW3052055975

What OpenQuestion holds

Textmetadata
LicenceCC0
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.