Evidence map›Paper›PMID 21636640›Full record

ArticleJournal of the American Society of Nephrology : JASN2011

Inhibition of the P2X7 receptor reduces cystogenesis in PKD.

Ming-Yang Chang, Jenn-Kan Lu, Ya-Chung Tian, Yung-Chang Chen, Cheng-Chieh Hung, Yi-Hui Huang, Yau-Hung Chen, Mai-Szu Wu, Chih-Wei Yang, Yi-Chuan Cheng

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Pannexin channels in the kidney.American journal of physiology. Renal physiology · 2025
    Review
  3. Calcium signalling and transport in the kidney.Nature reviews. Nephrology · 2024
    Review
  4. Article
  5. Article
  6. Animal Models for the Investigation of P2X7 Receptors.International journal of molecular sciences · 2023
    Review
  7. Modulation of P2XPhysiological reports · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Knockout ofAmerican journal of physiology. Renal physiology · 2019
    Article
  18. Associations ofJDR clinical and translational research · 2019
    Article
  19. Article
  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

10 authors at 5 institutions in 1 country.

Ming-Yang ChangKidney Research Center, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Jenn-Kan Lu
Ya-Chung Tian
Yung-Chang Chen
Cheng-Chieh Hung
Yi-Hui Huang
Yau-Hung Chen
Mai-Szu Wu
Chih-Wei Yang
Yi-Chuan Cheng
Chang Gung University · TWChang Gung Memorial Hospital · TWKeelung Chang Gung Memorial Hospital · TWNational Taiwan Ocean University · TWTamkang University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The P2X7 receptor participates in purinergic signaling, which may promote the progression of ADPKD. We examined the effects of a P2X7 receptor antagonist and a P2X7 receptor agonist on cyst development in a zebrafish model of polycystic kidney disease in which we knocked down pkd2 by morpholinos. We used live wt-1b pronephric-specific GFP-expressing zebrafish embryos to directly observe changes in the pronephros. Exposure of pkd2-morphant zebrafish to a P2X7 receptor antagonist (oxidized ATP [OxATP]) significantly reduced the frequency of the cystic phenotype compared with either exposure to a P2X7 receptor agonist (BzATP) or with no treatment (P < 0.01). Histology confirmed improvement of glomerular cysts in OxATP-treated pkd2 morphants. OxATP also reduced p-ERK activity and cell proliferation in pronephric kidneys in pkd2 morphants. Inhibition of P2X7 with an additional specific antagonist (A-438079), and through morpholino-mediated knockdown of p2rx7, confirmed these effects. In conclusion, blockade of the P2X7 receptor reduces cyst formation via ERK-dependent pathways in a zebrafish model of polycystic kidney disease, suggesting that P2X7 antagonists may have therapeutic potential in ADPKD.

Indexed as

Adenosine TriphosphateAnimalsCell ProliferationCiliaDisease Models, AnimalEpithelial CellsExtracellular Signal-Regulated MAP KinasesGene Knockdown TechniquesHumansInterleukin-1betaKidney Tubules, ProximalMAP Kinase Signaling SystemPhenotypePolycystic Kidney, Autosomal DominantPurinergic P2X Receptor AgonistsPurinergic P2X Receptor Antagonists2',3'-dialdehyde ATP3-(5-(2,3-dichlorophenyl)-1H-tetrazol-1-yl)methylpyridine3'-O-(4-benzoyl)benzoyladenosine 5'-triphosphateAdenosine TriphosphateExtracellular Signal-Regulated MAP KinasesInterleukin-1betaPurinergic P2X Receptor AgonistsPurinergic P2X Receptor AntagonistsPyridinesReceptors, Purinergic P2X7RNA, MessengerTetrazoles

Identifiers

PMID21636640
PMCPMC3171940
OpenAlexW2170365142

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.