Evidence map›Paper›PMID 25830347›Full record

ArticlePloS one2015

Pharmacological inhibition of FTO.

Fiona McMurray, Marina Demetriades, WeiShen Aik, Myrte Merkestein, Holger Kramer, Daniel S Andrew, Cheryl L Scudamore, Tertius A Hough, Sara Wells, Frances M Ashcroft and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Targeting DTX2/UFD1-mediated FTO degradation to regulate antitumor immunity.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Review
  4. Review
  5. m6A demethylase FTO and osteoporosis: potential therapeutic interventions.Frontiers in cell and developmental biology · 2023
    Review
  6. Review
  7. Review
  8. The Key Role of RNA Modification in Breast Cancer.Frontiers in cell and developmental biology · 2022
    Review
  9. Article
  10. Review
  11. NCell proliferation · 2020
    Review
  12. Article
  13. It's complicated… mBiochimica et biophysica acta. Gene regulatory mechanisms · 2019
    Review
  14. Article
  15. Regulatory Role of RNA NFrontiers in endocrinology · 2019
    Review
  16. mFrontiers in oncology · 2019
    Article
  17. Acta pharmaceutica Sinica. B · 2018
    Review
  18. FTO demethylase activity is essential for normal bone growth and bone mineralization in mice.Biochimica et biophysica acta. Molecular basis of disease · 2018
    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

13 authors at 3 institutions in 1 country.

Fiona McMurrayMRC Harwell, Harwell Oxford Campus, Oxfordshire, Oxford, OX11 0RD, United Kingdom.
Marina DemetriadesChemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, United Kingdom.
WeiShen AikChemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, United Kingdom.
Myrte MerkesteinHenry Wellcome Centre for Gene Function, Department of Physiology, Anatomy and Genetics, University of Oxford, Parks Road, Oxford, OX1 3PT, United Kingdom.
Holger KramerHenry Wellcome Centre for Gene Function, Department of Physiology, Anatomy and Genetics, University of Oxford, Parks Road, Oxford, OX1 3PT, United Kingdom.
Daniel S AndrewMRC Harwell, Harwell Oxford Campus, Oxfordshire, Oxford, OX11 0RD, United Kingdom.
Cheryl L ScudamoreMRC Harwell, Harwell Oxford Campus, Oxfordshire, Oxford, OX11 0RD, United Kingdom.
Tertius A HoughMRC Harwell, Harwell Oxford Campus, Oxfordshire, Oxford, OX11 0RD, United Kingdom.
Sara WellsMRC Harwell, Harwell Oxford Campus, Oxfordshire, Oxford, OX11 0RD, United Kingdom.
Frances M AshcroftHenry Wellcome Centre for Gene Function, Department of Physiology, Anatomy and Genetics, University of Oxford, Parks Road, Oxford, OX1 3PT, United Kingdom.
Michael A McDonoughChemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, United Kingdom.
Christopher J SchofieldChemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, United Kingdom.
Roger D CoxMRC Harwell, Harwell Oxford Campus, Oxfordshire, Oxford, OX11 0RD, United Kingdom.
Mary Lyon Centre at MRC Harwell · GBUniversity of Oxford · GBCentre for Human Genetics · GB

Funding

Medical Research Council G0901338Medical Research Council MC_U142661184Medical Research Council MC_UP_1502/1Wellcome Trust 084655Wellcome Trust 093136
6 · The paper itself

Abstract

In 2007, a genome wide association study identified a SNP in intron one of the gene encoding human FTO that was associated with increased body mass index. Homozygous risk allele carriers are on average three kg heavier than those homozygous for the protective allele. FTO is a DNA/RNA demethylase, however, how this function affects body weight, if at all, is unknown. Here we aimed to pharmacologically inhibit FTO to examine the effect of its demethylase function in vitro and in vivo as a first step in evaluating the therapeutic potential of FTO. We showed that IOX3, a known inhibitor of the HIF prolyl hydroxylases, decreased protein expression of FTO (in C2C12 cells) and reduced maximal respiration rate in vitro. However, FTO protein levels were not significantly altered by treatment of mice with IOX3 at 60 mg/kg every two days. This treatment did not affect body weight, or RER, but did significantly reduce bone mineral density and content and alter adipose tissue distribution. Future compounds designed to selectively inhibit FTO's demethylase activity could be therapeutically useful for the treatment of obesity.

Indexed as

Alpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsAnti-Obesity AgentsCell LineDrug Evaluation, PreclinicalGlycineInhibitory Concentration 50IsoquinolinesMaleMice, Inbred C57BLMixed Function OxygenasesObesityOxo-Acid-Lyases(1-chloro-4-hydroxyisoquinoline-3-carbonyl)amino)acetic acidAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnti-Obesity AgentsFTO protein, mouseGlycineIsoquinolinesMixed Function OxygenasesOxo-Acid-Lyases

Identifiers

PMID25830347
PMCPMC4382163
OpenAlexW2080178850

What OpenQuestion holds

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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.