Evidence map›Paper›PMID 20130528›Full record

ReviewKidney international2010

Toward the development of podocyte-specific drugs.

Jochen Reiser, Vineet Gupta, Andreas D Kistler

Open access · bronzeAbstract readReview
In one paragraph

Review in Kidney international, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Renal cell markers: lighthouses for managing renal diseases.American journal of physiology. Renal physiology · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Stop that podocyte!American journal of physiology. Renal physiology · 2017
    Article
  14. Article
  15. Podocytes.F1000Research · 2016
    Review
  16. A Podocyte-Based Automated Screening Assay Identifies Protective Small Molecules.Journal of the American Society of Nephrology : JASN · 2015
    Article
  17. Article
  18. Sirtuin1 Maintains Actin Cytoskeleton by Deacetylation of Cortactin in Injured Podocytes.Journal of the American Society of Nephrology : JASN · 2015
    Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Jochen ReiserDivision of Nephrology and Hypertension, University of Miami Miller School of Medicine, Miami, Florida 33136, USA. jreiser@med.miami.edu
Vineet Gupta
Andreas D Kistler
University of Miami · US

Funding

Proteolytic Regulation of Podocyte Function by Cathepsin L.R01DK073495 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI REISER, JOCHEN · 2006 to 2015
$2.4M
Beta2 Integrin Activation and SignalingK01DK068253 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GUPTA, VINEET · 2004 to 2010
$709k
HTS Assay for Discovery:Small Molecule Regulators (RMI)R03NS053659 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI GUPTA, VINEET · 2005 to 2005
$88k
NIDDK NIH HHS DK073495NIDDK NIH HHS K01 DK068253NIDDK NIH HHS K01DK068253NIDDK NIH HHS R01 DK073495NINDS NIH HHS R03 NS053659NINDS NIH HHS R03NS053659
6 · The paper itself

Abstract

Most kidney diseases that ultimately lead to end-stage renal failure originate within the glomerulus and are associated with proteinuria. Treatment options are unspecific and offer partial cures at best because available therapies do not primarily treat glomerular cells but rather act systemically and thus cause many side effects. Most glomerulopathies directly stem from injury to podocytes, cells that have a key role in the maintenance of the glomerular filter. Thus, these cells constitute an obvious and promising target for the development of novel kidney-protective drugs. During the last decade, enormous advances have been made in the understanding of podocyte structure and function. A number of pathways that are altered during glomerular diseases may be targeted by novel small- and large-molecule drugs as well as biologicals that have been identified in nephrology and other areas of drug development. Cultured podocytes provide a valuable model for high-throughput drug screening assays. Furthermore, podocytes have been shown to possess many features that make them particularly good target cells for renal protection. This mini-review discusses some of the most recent promising data related to potential drug therapy for proteinuria and kidney disease through direct podocyte targeting.

Indexed as

Dosage FormsKidneyKidney DiseasesKidney Failure, ChronicKidney GlomerulusPharmaceutical PreparationsPhysiological PhenomenaPodocytesProteinuriaDosage FormsPharmaceutical Preparations

Identifiers

PMID20130528
PMCPMC4089392
OpenAlexW1970138917

What OpenQuestion holds

Textmetadata
LicenceTDM
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.