Evidence map›Paper›PMID 28955862›Full record

ArticleBiochemistry and biophysics reports2016

Increased level of phosphorylated desmin and its degradation products in heart failure.

Marion Bouvet, Emilie Dubois-Deruy, Tchilabalo Dilezitoko Alayi, Paul Mulder, Myriam El Amranii, Olivia Beseme, Philippe Amouyel, Vincent Richard, Stanislas Tomavo, Florence Pinet

Open access · goldAbstract read
In one paragraph

Article in Biochemistry and biophysics reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Marion BouvetINSERM, U1167, University Lille, Institut Pasteur de Lille, F-59000 Lille, France.
Emilie Dubois-DeruyINSERM, U1167, University Lille, Institut Pasteur de Lille, F-59000 Lille, France.
Tchilabalo Dilezitoko AlayiUniversity Lille, CNRS UMR8204, INSERM, U1019, Institut Pasteur de Lille, Plateforme de Protéomique et des Peptides Modifiés (P3M), F-59000 Lille, France.
Paul MulderINSERM, U1096, University of Rouen, Institute for Research and Innovation in Biomedicine, F-76000 Rouen, France.
Myriam El AmraniiUniversity Lille, CNRS UMR8204, INSERM, U1019, Institut Pasteur de Lille, Plateforme de Protéomique et des Peptides Modifiés (P3M), F-59000 Lille, France.
Olivia BesemeINSERM, U1167, University Lille, Institut Pasteur de Lille, F-59000 Lille, France.
Philippe AmouyelINSERM, U1167, University Lille, Institut Pasteur de Lille, Centre Hospitalier Régional et Universitaire de Lille, F-59000 Lille, France.
Vincent RichardINSERM, U1096, University of Rouen, Institute for Research and Innovation in Biomedicine, F-76000 Rouen, France.
Stanislas TomavoUniversity Lille, CNRS UMR8204, INSERM, U1019, Institut Pasteur de Lille, Plateforme de Protéomique et des Peptides Modifiés (P3M), F-59000 Lille, France.
Florence PinetINSERM, U1167, University Lille, Institut Pasteur de Lille, F-59000 Lille, France.
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although several risk factors such as infarct size have been identified, the progression/severity of heart failure (HF) remains difficult to predict in clinical practice. Using an experimental rat model of ischemic HF and phosphoproteomic technology, we found an increased level of phosphorylated desmin in the left ventricle (LV) of HF-rats. The purpose of the present work is to assess whether desmin is a circulating or only a tissue biomarker of HF. We used several antibodies in order to detect desmin, its proteolytic fragments and its phosphorylated form in LV and plasma by western blot, phosphate affinity electrophoresis, mass spectrometry and immunofluorescence. Plasma was treated with combinatorial peptide ligand library or depleted for albumin and immunoglobulins to increase the sensitivity of detection. We found a 2-fold increased serine-desmin phosphorylation in the LV of HF-rats, mainly in the insoluble fraction, suggesting the formation of desmin aggregates. Desmin cleavage products were also detected in the LV of HF rats, indicating that the increased phosphorylation of desmin results in more susceptibility to proteolytic activity, likely mediated by calpain activity. The native desmin and its degradation products were undetectable in the plasma of rat, mouse or human. These data suggest the potential of serine-phosphorylated form of desmin and its degradation products, but not of desmin itself, as tissue but not circulating biomarkers of HF.

Indexed as

DesminHeart failureMass spectrometryPhosphorylationPlasmaWestern blot

Identifiers

PMID28955862
PMCPMC5600436
OpenAlexW2297449224

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.