Evidence map›Paper›PMID 32197499›Full record

ArticleInternational journal of molecular sciences2020

ECM Characterization Reveals a Massive Activation of Acute Phase Response during FSGS.

Eva Nora Bukosza, Christoph Kornauth, Karin Hummel, Helga Schachner, Nicole Huttary, Sigurd Krieger, Katharina Nöbauer, André Oszwald, Ebrahim Razzazi Fazeli, Klaus Kratochwill and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Precision medicine for focal segmental glomerulosclerosis.Kidney research and clinical practice · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Observational
  10. Review
  11. Article
  12. Article
  13. Effect of tacrolimus on the expression of Park7 in glomerular podocytes injured by puromycin aminonucleoside.Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    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

14 authors at 4 institutions in 2 countries.

Eva Nora BukoszaInstitute of Translational Medicine, Semmelweis University Budapest, Tűzoltó u 37-47, 1094 Budapest, Hungary.
Christoph KornauthClinical Institute for Pathology, Medical University Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Karin HummelVetcore Facility for Research, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, Austria.
Helga SchachnerClinical Institute for Pathology, Medical University Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Nicole HuttaryClinical Institute for Pathology, Medical University Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Sigurd KriegerClinical Institute for Pathology, Medical University Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Katharina NöbauerVetcore Facility for Research, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, Austria.
André OszwaldClinical Institute for Pathology, Medical University Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Ebrahim Razzazi FazeliVetcore Facility for Research, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, Austria.
Klaus KratochwillChristian Doppler Laboratory for Molecular Stress Research in Peritoneal Dialysis, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, 1210 Vienna, Austria.ORCID 0000-0003-0803-614X
Christoph AufrichtDivision of Pediatric Nephrology and Gastroenterology, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, 1210 Vienna, Austria.
Gabor SzénásiInstitute of Translational Medicine, Semmelweis University Budapest, Tűzoltó u 37-47, 1094 Budapest, Hungary.
Peter HamarInstitute of Translational Medicine, Semmelweis University Budapest, Tűzoltó u 37-47, 1094 Budapest, Hungary.
Christoph A GebeshuberClinical Institute for Pathology, Medical University Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Medical University of Vienna · ATSemmelweis University · HUUniversity of Veterinary Medicine Vienna · ATChristian Doppler Laboratory for Thermoelectricity · AT

Funding

Action Austria-Hungary Foundation (Stiftung Aktion Österreich-Ungarn, Wissenschafts- und Erziehungskooperation (Stiftung AÖU - 90 ÖU15)Economic Development and Innovation Operative Program Grant GINOP 2.3.2-15-2016-00048 (PH)Hungarian Scientific Research Fund OTKA SNN-114619 (PH); ANN-110810 (PH)National Research,Development and Innovation Fund of Hungary NVKP_16-1-2016-0042 (PH)University of Pécs ,the Kispál Gyula startup grant (300021)
6 · The paper itself

Abstract

The glomerular basement membrane (GBM) and extra-cellular matrix (ECM) are essential to maintain a functional interaction between the glomerular podocytes and the fenestrated endothelial cells in the formation of the slit diaphragm for the filtration of blood. Dysregulation of ECM homeostasis can cause Focal segmental glomerulosclerosis (FSGS). Despite this central role, alterations in ECM composition during FSGS have not been analyzed in detail yet. Here, we characterized the ECM proteome changes in miR-193a-overexpressing mice, which suffer from FSGS due to suppression of Wilms' tumor 1 (WT1). By mass spectrometry we identified a massive activation of the acute phase response, especially the complement and fibrinogen pathways. Several protease inhibitors (ITIH1, SERPINA1, SERPINA3) were also strongly increased. Complementary analysis of RNA expression data from both miR-193a mice and human FSGS patients identified additional candidate genes also mainly involved in the acute phase response. In total, we identified more than 60 dysregulated, ECM-associated genes with potential relevance for FSGS progression. Our comprehensive analysis of a murine FSGS model and translational comparison with human data offers novel targets for FSGS therapy.

Indexed as

AnimalsComplement System ProteinsDisease Models, AnimalExtracellular MatrixFibrinogenGene Expression RegulationGlomerulosclerosis, Focal SegmentalMiceMice, Inbred BALB CMice, TransgenicMicroRNAsProtease InhibitorsComplement System ProteinsFibrinogenMicroRNAsMIRN193 microRNA, mouseProtease Inhibitorsacute phase responsecomplement systemECMfibrinogenFSGSsclerosis

Identifiers

PMID32197499
PMCPMC7139641
OpenAlexW3011594588

What Socratic 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 Socratic graph.