Evidence map›Paper›PMID 27118870›Full record

ArticleThe Biochemical journal2016

FAP finds FGF21 easy to digest.

Matthew P Gillum, Matthew J Potthoff

Open access · greenAbstract readComment
In one paragraph

Article in The Biochemical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Matthew P GillumSection for Liver Metabolism and Metabolic Imaging, the Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, 2200 Copenhagen, Denmark Department of Biomedical Sciences, the Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, 2200 Copenhagen, Denmark gillum@sund.ku.dk matthew-potthoff@uiowa.edu.
Matthew J PotthoffDepartment of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA 52242, U.S.A. Fraternal Order of Eagles Diabetes Research Center, University of Iowa Carver College of Medicine, Iowa City, IA 52242, U.S.A. gillum@sund.ku.dk matthew-potthoff@uiowa.edu.
Novo Nordisk Foundation · DK

Funding

Regulation of Metabolism by FGF21R01DK106104 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Matthew Joseph Potthoff · 2015 to 2026
$6.2M
NIDDK NIH HHS R01 DK106104
6 · The paper itself

Abstract

Fibroblast growth factor 21 (FGF21) is an endocrine hormone that regulates carbohydrate and lipid metabolism. In humans, circulating FGF21 is inactivated by proteolytic cleavage of its C-terminus, thereby preventing signalling through a receptor complex. The mechanism for this cleavage event and the factors contributing to the post-translational regulation of FGF21 activity has previously been unknown. In a recent issue of the Biochemical Journal, Zhen et al. have identified fibroblast activation protein (FAP) as the endopeptidase responsible for this site-specific cleavage of human FGF21 (hFGF21), and propose that inhibition of FAP may be a therapeutic strategy to increase endogenous levels of active FGF21.

Indexed as

ProteolysisEndopeptidasesFibroblast Activation Protein AlphaFibroblast Growth FactorsGelatinasesHumansMembrane ProteinsProtein DomainsSerine EndopeptidasesEndopeptidasesFibroblast Activation Protein Alphafibroblast growth factor 21Fibroblast Growth FactorsGelatinasesMembrane ProteinsSerine Endopeptidasesdipeptidyl peptidase IV (DPP-IV)fibroblast activation protein (FAP)fibroblast growth factor 21 (FGF21)proteolytic cleavage

Identifiers

PMID27118870
PMCPMC7721556
OpenAlexW2342510554

What OpenQuestion holds

Textmetadata
LicenceTDM
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.