Evidence map›Paper›PMID 25427253›Full record

ArticlePloS one2014

Monoclonal antibody targeting of fibroblast growth factor receptor 1c ameliorates obesity and glucose intolerance via central mechanisms.

Christopher J Lelliott, Andrea Ahnmark, Therese Admyre, Ingela Ahlstedt, Lorraine Irving, Feenagh Keyes, Laurel Patterson, Michael B Mumphrey, Mikael Bjursell, Tracy Gorman and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  3. Review
  4. JHEP reports : innovation in hepatology · 2020
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  7. A Long-Acting PYYCell metabolism · 2019
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  10. Does gastric bypass surgery change body weight set point?International journal of obesity supplements · 2016
    Review
  11. Article
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  14. Article
  15. Review
  16. 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 4 institutions in 3 countries.

Christopher J LelliottCardiovascular & Metabolic Disease Innovative Medicines, Dept of Bioscience Diabetes, AstraZeneca, Mölndal, Sweden.
Andrea AhnmarkCardiovascular & Metabolic Disease Innovative Medicines, Dept of Bioscience Diabetes, AstraZeneca, Mölndal, Sweden.
Therese AdmyreDiscovery Sciences Transgenics, AstraZeneca, Mölndal, Sweden.
Ingela AhlstedtCardiovascular & Metabolic Disease Innovative Medicines, Dept of Bioscience Diabetes, AstraZeneca, Mölndal, Sweden.
Lorraine IrvingAntibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom.
Feenagh KeyesAntibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom.
Laurel PattersonNeurobiology of Nutrition Laboratory, Pennington Biomedical Research Center, Baton Rouge, United States of America.
Michael B MumphreyNeurobiology of Nutrition Laboratory, Pennington Biomedical Research Center, Baton Rouge, United States of America.
Mikael BjursellDiscovery Sciences Transgenics, AstraZeneca, Mölndal, Sweden.
Tracy GormanAstraZeneca, Discovery Sciences, Mereside, Alderley Park, Macclesfield, Cheshire, United Kingdom.
Mohammad Bohlooly-YDiscovery Sciences Transgenics, AstraZeneca, Mölndal, Sweden.
Andrew BuchananAntibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom.
Paula HarrisonAntibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom.
Tristan VaughanAntibody Discovery and Protein Engineering, MedImmune, Cambridge, United Kingdom.
Hans-Rudolf BerthoudNeurobiology of Nutrition Laboratory, Pennington Biomedical Research Center, Baton Rouge, United States of America.
Daniel LindénCardiovascular & Metabolic Disease Innovative Medicines, Dept of Bioscience Diabetes, AstraZeneca, Mölndal, Sweden.
AstraZeneca (Sweden) · SERecombinant Antibody Technology (United Kingdom) · GBPennington Biomedical Research Center · USAstraZeneca (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have generated a novel monoclonal antibody targeting human FGFR1c (R1c mAb) that caused profound body weight and body fat loss in diet-induced obese mice due to decreased food intake (with energy expenditure unaltered), in turn improving glucose control. R1c mAb also caused weight loss in leptin-deficient ob/ob mice, leptin receptor-mutant db/db mice, and in mice lacking either the melanocortin 4 receptor or the melanin-concentrating hormone receptor 1. In addition, R1c mAb did not change hypothalamic mRNA expression levels of Agrp, Cart, Pomc, Npy, Crh, Mch, or Orexin, suggesting that R1c mAb could cause food intake inhibition and body weight loss via other mechanisms in the brain. Interestingly, peripherally administered R1c mAb accumulated in the median eminence, adjacent arcuate nucleus and in the circumventricular organs where it activated the early response gene c-Fos. As a plausible mechanism and coinciding with the initiation of food intake suppression, R1c mAb induced hypothalamic expression levels of the cytokines Monocyte chemoattractant protein 1 and 3 and ERK1/2 and p70 S6 kinase 1 activation.

Indexed as

AnimalsAntibodies, MonoclonalArcuate Nucleus of HypothalamusChemokine CCL2Chemokine CCL7Circumventricular OrgansEatingEnergy MetabolismFemaleGene Expression RegulationGlucose IntoleranceHumansHypothalamusLeptinMiceMice, KnockoutAntibodies, MonoclonalChemokine CCL2Chemokine CCL7FGFR1 protein, humanLeptinMC4R protein, mouseMchr1 protein, mouseMitogen-Activated Protein KinasesReceptor, Fibroblast Growth Factor, Type 1Receptor, Melanocortin, Type 4Receptors, SomatostatinRibosomal Protein S6 Kinases, 70-kDaSerum Response Factor

Identifiers

PMID25427253
PMCPMC4245083
OpenAlexW2026300445

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.