Evidence map›Paper›PMID 15782307›Full record

ArticlePediatric nephrology (Berlin, Germany)2005

Dysregulation of renal MMP-3 and MMP-7 in canine X-linked Alport syndrome.

Velidi H Rao, George E Lees, Clifford E Kashtan, Duane C Delimont, Rakesh Singh, Daniel T Meehan, Gautam Bhattacharya, Brian R Berridge, Dominic Cosgrove

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Genotype-Based Molecular Mechanisms in Alport Syndrome.Journal of the American Society of Nephrology : JASN · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Soluble biglycan as a biomarker of inflammatory renal diseases.The international journal of biochemistry & cell biology · 2014
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Gene expression analysis in a canine model of X-linked Alport syndrome.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  11. Article
  12. 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

9 authors at 6 institutions in 2 countries.

Velidi H RaoDepartment of Genetics, Boys Town National Research Hospital, Omaha, NE 68131, USA.
George E Lees
Clifford E Kashtan
Duane C Delimont
Rakesh Singh
Daniel T Meehan
Gautam Bhattacharya
Brian R Berridge
Dominic Cosgrove
Boys Town National Research Hospital · USBoys Town · USGreenfield Research (Canada) · CATexas A&M University · USUniversity of Minnesota Medical Center · USUniversity of Nebraska Medical Center · US

Funding

MOLECULAR ASPECTS OF ALPORT RENAL DISEASE PROGRESSIONR01DK055000 · NIDDK · FATHER FLANAGAN'S BOYS'HOME · PI COSGROVE, DOMINIC E. · 1999 to 2013
$3.0M
GLOMERULAR PERMSELECTIVITY IN ALPORT SYNDROMER01DK057676 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI KASHTAN, CLIFFORD E · 2000 to 2004
$1.5M
NIDDK NIH HHS R01 DK55000NIDDK NIH HHS R01 DK57676
6 · The paper itself

Abstract

Matrix metalloproteinases (MMPs) play an important regulatory role in many biological and pathological processes and their specific role in Alport syndrome (AS) is not yet clearly defined. In this study, the naturally occurring canine X-linked AS was used to demonstrate a potential role for MMP-3 and MMP-7 in Alport renal pathogenesis. Recently, we demonstrated that the expression of MMP-2, MMP-9 and MMP-14 was upregulated in the renal cortex of dogs with a spontaneous form of XLAS. In the present study, we examined necropsy samples of renal cortex from normal and XLAS dogs for MMP-3 and MMP-7 as they have the potential to activate MMP-2 and MMP-9. Immunohistochemical analysis showed strong immunostaining for both MMP-3 and MMP-7 in the interstitial space of XLAS kidneys, while virtually no immunostaining was observed in similar fields from normal dogs. RT-PCR and casein zymography confirmed that both mRNA transcripts and activities of MMP-3 and MMP-7 are elevated in XLAS kidneys. The induction of these MMPs likely contributes to tissue destruction associated with the fibrogenic process, while augmenting the activation of MMP-2 and MMP-9 by MMP-3 and MMP-7 in XLAS. Thus, these data further implicate a role for the MMPs in progressive renal pathogenesis associated with AS.

Indexed as

Genetic LinkageX ChromosomeAnimalsDog DiseasesDogsKidneyMatrix Metalloproteinase 3Matrix Metalloproteinase 7Matrix MetalloproteinasesNephritis, HereditaryMatrix Metalloproteinase 3Matrix Metalloproteinase 7Matrix Metalloproteinases

Identifiers

PMID15782307
OpenAlexW2145088738

What OpenQuestion holds

Textmetadata
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.