Evidence map›Paper›PMID 23668934›Full record

ArticleZebrafish2013

The zebrafish as a model to study polycystic liver disease.

Pamela S Tietz Bogert, Bing Q Huang, Sergio A Gradilone, Tetyana V Masyuk, Gary L Moulder, Stephen C Ekker, Nicholas F Larusso

Open access · greenAbstract read
In one paragraph

Article in Zebrafish, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Somatostatin in renal physiology and autosomal dominant polycystic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2020
    Review
  5. Review
  6. microRNA-1 Regulates NCC Migration and Differentiation by TargetingInternational journal of biological sciences · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Identification and Expression Analysis of the Complete Family of ZebrafishFrontiers in cell and developmental biology · 2017
    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

7 authors at 2 institutions in 1 country.

Pamela S Tietz BogertDivision of Gastroenterology and Hepatology, Mayo Clinic College of Medicine , Rochester, MN 55905, USA.
Bing Q Huang
Sergio A Gradilone
Tetyana V Masyuk
Gary L Moulder
Stephen C Ekker
Nicholas F Larusso
Mayo Clinic · USMayo Clinic in Arizona · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
The Pathobiology of Hepatic EpitheliaR01DK024031 · NIDDK · MAYO CLINIC ROCHESTER · PI LARUSSO, NICHOLAS F. · 1986 to 2023
$10.4M
PATHOBIOLOGY OF HEPATIC EPITHELIAR37DK024031 · NIDDK · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI LARUSSO, NICHOLAS F. · 1991 to 1998
–
NIDDK NIH HHS DK24031NIDDK NIH HHS P30 DK084567NIDDK NIH HHS P30DK084567
6 · The paper itself

Abstract

In the polycystic liver diseases (PLD), genetic defects initiate the formation of cysts in the liver and kidney. In rodent models of PLD (i.e., the PCK rat and Pkd2(WS25/-) mouse), we have studied hepatorenal cystic disease and therapeutic approaches. In this study, we employed zebrafish injected with morpholinos against genes involved in the PLD, including sec63, prkcsh, and pkd1a. We calculated the liver cystic area, and based on our rodent studies, we exposed the embryos to pasireotide [1 μM] or vitamin K3 [100 μM] and assessed the endoplasmic reticulum (ER) in cholangiocytes in embryos treated with 4-phenylbutyrate (4-PBA). Our results show that (a) morpholinos against sec63, prkcsh, and pkd1a eliminate expression of the respective proteins; (b) phenotypic body changes included curved tail and the formation of hepatic cysts in zebrafish larvae; (c) exposure of embryos to pasireotide inhibited hepatic cystogenesis in the zebrafish models; and (d) exposure of embryos to 4-PBA resulted in the ER in cholangiocytes resolving from a curved to a smooth appearance. Our results suggest that the zebrafish model of PLD may provide a means to screen drugs that could inhibit hepatic cystogenesis.

Indexed as

Disease Models, AnimalGene Expression Regulation, NeoplasticZebrafishAnimalsAntineoplastic AgentsCalcium-Binding ProteinsCystsDNA HelicasesGlucosidasesHumansIntracellular Signaling Peptides and ProteinsLarvaLiver DiseasesMorpholinosPhenylbutyratesPolycystic Kidney, Autosomal Dominant4-phenylbutyric acidAntineoplastic AgentsCalcium-Binding ProteinsDNA HelicasesGlucosidasesHFM1 protein, humanIntracellular Signaling Peptides and ProteinsMorpholinospasireotidePhenylbutyratesPRKCSH protein, humanSomatostatinTRPP Cation ChannelsVitamin K 3

Identifiers

PMID23668934
PMCPMC3673589
OpenAlexW2023786092

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.