Evidence map›Paper›PMID 28793886›Full record

ArticleBMC pulmonary medicine2017

Cathepsin-S degraded decorin are elevated in fibrotic lung disorders - development and biological validation of a new serum biomarker.

S N Kehlet, C L Bager, N Willumsen, B Dasgupta, C Brodmerkel, M Curran, S Brix, D J Leeming, M A Karsdal

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

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  7. Biomimetic strategies for the deputization of proteoglycan functions.Frontiers in cell and developmental biology · 2024
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  12. Role of the extracellular matrix in COVID-19.World journal of clinical cases · 2023
    Review
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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

9 authors at 3 institutions in 2 countries.

S N KehletNordic Bioscience A/S, Herlev, Denmark. snk@nordicbio.com.
C L BagerProscion A/S, Herlev, Denmark.
N WillumsenNordic Bioscience A/S, Herlev, Denmark.
B DasguptaJanssen Pharmaceutical Companies of J & J, LLC, Springhouse, PA, USA.
C BrodmerkelJanssen Pharmaceutical Companies of J & J, LLC, Springhouse, PA, USA.
M CurranJanssen Pharmaceutical Companies of J & J, LLC, Springhouse, PA, USA.
S BrixDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Kongens Lyngby, Denmark.
D J LeemingNordic Bioscience A/S, Herlev, Denmark.
M A KarsdalNordic Bioscience A/S, Herlev, Denmark.
Nordic Bioscience (Denmark) · DKSpringhouse · USTechnical University of Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDecorin is one of the most abundant proteoglycans of the extracellular matrix and is mainly secreted and deposited in the interstitial matrix by fibroblasts where it plays an important role in collagen turnover and tissue homeostasis. Degradation of decorin might disturb normal tissue homeostasis contributing to extracellular matrix remodeling diseases. Here, we present the development and validation of a competitive enzyme-linked immunosorbent assay (ELISA) quantifying a specific fragment of degraded decorin, which has potential as a novel non-invasive serum biomarker for fibrotic lung disorders.

methodsA fragment of decorin cleaved in vitro using human articular cartilage was identified by mass-spectrometry (MS/MS). Monoclonal antibodies were raised against the neo-epitope of the cleaved decorin fragment and a competitive ELISA assay (DCN-CS) was developed. The assay was evaluated by determining the inter- and intra-assay precision, dilution recovery, accuracy, analyte stability and interference. Serum levels were assessed in lung cancer patients, patients with idiopathic pulmonary fibrosis (IPF), patients with chronic obstructive pulmonary disease (COPD) and healthy controls.

resultsThe DCN-CS ELISA was technically robust and was specific for decorin cleaved by cathepsin-S. DCN-CS was elevated in lung cancer patients (p < 0.0001) and IPF patients (p < 0.001) when compared to healthy controls. The diagnostic power for differentiating lung cancer patients and IPF patients from healthy controls was 0.96 and 0.77, respectively.

conclusionCathepsin-S degraded decorin could be quantified in serum using the DCN-CS competitive ELISA. The clinical data indicated that degradation of decorin by cathepsin-S is an important part of the pathology of lung cancer and IPF.

Indexed as

AdultAgedAged, 80 and overBiomarkersCarcinoma, Non-Small-Cell LungCase-Control StudiesCathepsinsDecorinEnzyme-Linked Immunosorbent AssayFemaleHumansIdiopathic Pulmonary FibrosisLung NeoplasmsMaleMiddle AgedPeptide FragmentsBiomarkerscathepsin SCathepsinsDCN protein, humanDecorinPeptide FragmentsCancerCathepsin-SDecorinExtracellular matrixIdiopathic pulmonary fibrosisSerum biomarker

Identifiers

PMID28793886
PMCPMC5550991
OpenAlexW2744359875

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.