Evidence map›Paper›PMID 29617647›Full record

ArticleCell metabolism2018

The Factor Inhibiting HIF Asparaginyl Hydroxylase Regulates Oxidative Metabolism and Accelerates Metabolic Adaptation to Hypoxia.

Jingwei Sim, Andrew S Cowburn, Asis Palazon, Basetti Madhu, Petros A Tyrakis, David Macías, David M Bargiela, Sandra Pietsch, Michael Gralla, Colin E Evans and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Cell metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

48 citing papers in PubMed, 87 citations in OpenAlex.

  1. Methylglyoxal AttenuatesInternational journal of molecular sciences · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Deficiency of factor-inhibiting HIF creates a tumor-promoting immune microenvironment.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Review
  12. Article
  13. Article
  14. Structure-guided optimisation ofChemical science · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Evolution of hypoxia and hypoxia-inducible factor asparaginyl hydroxylase regulation in chronic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2023
    Article
  19. Review
  20. Review
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

16 authors at 5 institutions in 4 countries.

Jingwei SimPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Andrew S CowburnPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Asis PalazonPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Basetti MadhuCancer Research UK Cambridge Institute, Cambridge CB2 0RE, UK.
Petros A TyrakisPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK; Cancer Research UK Cambridge Institute, Cambridge CB2 0RE, UK.
David MacíasPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
David M BargielaPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Sandra PietschPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Michael GrallaDepartment of Cell and Molecular Biology, Karolinska Institute, Stockholm SE-171 77, Sweden.
Colin E EvansPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Thaksaon KittipassornSchool of Biological Sciences, University of Adelaide, Adelaide, SA 5005, Australia; Department of Physiology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok 73170, Thailand.
Yu C J CheySchool of Biological Sciences, University of Adelaide, Adelaide, SA 5005, Australia.
Cristina M BrancoPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Helene RundqvistDepartment of Cell and Molecular Biology, Karolinska Institute, Stockholm SE-171 77, Sweden.
Daniel J PeetSchool of Biological Sciences, University of Adelaide, Adelaide, SA 5005, Australia.
Randall S JohnsonPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK; Department of Cell and Molecular Biology, Karolinska Institute, Stockholm SE-171 77, Sweden. Electronic address: rsj33@cam.ac.uk.
University of Cambridge · GBKarolinska Institutet · SEThe University of Adelaide · AUCancer Research UK Cambridge Center · GBSiriraj Hospital · TH

Funding

Wellcome TrustWellcome Trust 092738MA
6 · The paper itself

Abstract

Animals require an immediate response to oxygen availability to allow rapid shifts between oxidative and glycolytic metabolism. These metabolic shifts are highly regulated by the HIF transcription factor. The factor inhibiting HIF (FIH) is an asparaginyl hydroxylase that controls HIF transcriptional activity in an oxygen-dependent manner. We show here that FIH loss increases oxidative metabolism, while also increasing glycolytic capacity, and that this gives rise to an increase in oxygen consumption. We further show that the loss of FIH acts to accelerate the cellular metabolic response to hypoxia. Skeletal muscle expresses 50-fold higher levels of FIH than other tissues: we analyzed skeletal muscle FIH mutants and found a decreased metabolic efficiency, correlated with an increased oxidative rate and an increased rate of hypoxic response. We find that FIH, through its regulation of oxidation, acts in concert with the PHD/vHL pathway to accelerate HIF-mediated metabolic responses to hypoxia.

Indexed as

Adaptation, PhysiologicalAnimalsCell HypoxiaGene Expression RegulationGlycolysisHypoxia-Inducible Factor-Proline DioxygenasesMaleMiceMice, Inbred C57BLMixed Function OxygenasesOxygenOxygen ConsumptionProcollagen-Proline DioxygenaseSignal TransductionTranscription, GeneticVon Hippel-Lindau Tumor Suppressor ProteinEgln1 protein, mousefactor inhibiting hypoxia-inducible factor 1, mouseHypoxia-Inducible Factor-Proline DioxygenasesMixed Function OxygenasesOxygenPHD1 protein, mousePHD3 protein, mouseProcollagen-Proline DioxygenaseVHL protein, mouseVon Hippel-Lindau Tumor Suppressor ProteinHIFhypoxiametabolism

Identifiers

PMID29617647
PMCPMC5887987
OpenAlexW2795707995

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.