Evidence map›Paper›PMID 18815217›Full record

ArticleAmerican journal of physiology. Renal physiology2008

Urothelial expression of neuropilins and VEGF receptors in control and interstitial cystitis patients.

Ricardo Saban, Marcia R Saban, Julie Maier, Ben Fowler, Mark Tengowski, Carole A Davis, Xue-Ru Wu, Daniel J Culkin, Paul Hauser, Joseph Backer and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

34 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  10. Assessing bladder hyper-permeability biomarkersAmerican journal of nuclear medicine and molecular imaging · 2020
    Article
  11. Review
  12. Acyloxyacyl hydrolase modulates pelvic pain severity.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Article
  13. Article
  14. Review
  15. Article
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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

11 authors at 1 institution in 1 country.

Ricardo SabanCollege of Medicine, Univ. of Oklahoma Health Sciences Center (OUHSC Urinary Tract Physiological Genomics Laboratory, 800 Research Pkwy., Rm. 410, Oklahoma City, OK 73104, USA. ricardo-saban@ouhsc.edu
Marcia R Saban
Julie Maier
Ben Fowler
Mark Tengowski
Carole A Davis
Xue-Ru Wu
Daniel J Culkin
Paul Hauser
Joseph Backer
Robert E Hurst
University of Oklahoma Health Sciences Center · US

Funding

LPS-PEPTIDE INTERACTION IN BLADDER INFLAMMATIONR01DK055828 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SABAN, RICARDO · 1998 to 2007
$2.1M
Bladder transcriptome in experimental inflammationR01DK066101 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI SABAN, RICARDO · 2003 to 2007
$1.3M
Bladder transcriptome in experimental inflammationR56DK066101 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI SABAN, RICARDO · 2009 to 2009
$355k
NIDDK NIH HHS DK-066101-01NIDDK NIH HHS DK-55828-01
6 · The paper itself

Abstract

Interstitial cystitis (IC) is a chronic and painful bladder syndrome of unknown cause with no reliable biological marker or effective therapy. Vascular endothelial growth factor (VEGF), which plays a key role in bladder inflammation, is closely associated with the vascular alterations observed in patients with IC. However, our recent findings of VEGF receptors (VEGF-Rs) and VEGF coreceptors on nonendothelial cells in human and mouse urothelium suggest that additional VEGF targets and functions are possible in IC bladders. We report here that VEGF-Rs and coreceptors (neuropilins; NRP) are strongly expressed in both the human bladder urothelium and in the human bladder cancer cell line (J82) and that the expression of NRP2 and VEGF-R1 is significantly downregulated in IC compared with control subjects. In addition, treatment of J82 cells with bacillus Calmette-Guérin (BCG), a novel treatment strategy for IC, upregulates the messages for NRPs and VEGF-Rs. Furthermore, intravesical instillation of an internalizable VEGF fluorescent tracer (scVEGF/Cy5.5) into mouse urinary bladders results in a marked ligand accumulation in the urothelium and bladder parenchyma, indicating that urothelial VEGF-Rs are functionally active and capable of ligand interaction and internalization. Our results suggest that the VEGF pathway is altered in IC, that urinary VEGF may gain access to the bladder wall via these receptors, and that BCG treatment may replenish the missing VEGF-Rs/NRP receptors. Together, these results suggest that levels of NRPs, VEGF-Rs, and VEGF are new putative markers for the diagnosis of IC and that modulating these receptors can be exploited as therapeutic strategies.

Indexed as

AnimalsCell LineCystitis, InterstitialFemaleHumansInflammationMaleMiceNeuropilinsPolymerase Chain ReactionReceptors, Vascular Endothelial Growth FactorUrinary BladderVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-2NeuropilinsReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-2

Identifiers

PMID18815217
PMCPMC2604836
OpenAlexW2148906119

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.