Evidence map›Paper›PMID 22084084›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Chemical screen identifies FDA-approved drugs and target pathways that induce precocious pancreatic endocrine differentiation.

Meritxell Rovira, Wei Huang, Shamila Yusuff, Joong Sup Shim, Anthony A Ferrante, Jun O Liu, Michael J Parsons

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 91 citations in OpenAlex.

  1. Loss of function ofScience translational medicine · 2026
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  7. Review
  8. Animal models of silicosis: fishing for new therapeutic targets and treatments.European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  9. Zebrafish models of COVID-19.FEMS microbiology reviews · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. In vivo generation and regeneration of β cells in zebrafish.Cell regeneration (London, England) · 2020
    Review
  16. Article
  17. Modeling Lysosomal Storage Diseases in the Zebrafish.Frontiers in molecular biosciences · 2020
    Review
  18. Article
  19. Article
  20. Review
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 3 institutions in 2 countries.

Meritxell RoviraDepartment of Surgery, and McKusick-Nathans Institute for Genetic Medicine, The Johns Hopkins University, Baltimore, MD 21205, USA.
Wei Huang
Shamila Yusuff
Joong Sup Shim
Anthony A Ferrante
Jun O Liu
Michael J Parsons
Texas Endosurgery Institute · USLaboratory of Molecular Genetics · PLPhysical Sciences (United States) · US

Funding

JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI AHIMA, REXFORD S. · 2013 to 2017
$9.7M
Zebrafish CoreP01CA134292 · NCI · JOHNS HOPKINS UNIVERSITY · PI LEACH, STEVEN D · 2009 to 2013
$7.4M
Identifying the Progenitors Responsible for Beta Cell Regeneration in ZebrafishR01DK080730 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI PARSONS, MICHAEL J · 2008 to 2021
$4.5M
High-Throughput Screen For FDA Approved Drugs That Amplify Beta-Cell Mass In VivoRC4DK090816 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI HUSSAIN, MEHBOOB A, LIU, JUN O. · 2010 to 2010
$2.5M
Discovery and Investigation of Novel Angiogenesis Inhibitors Among Existing DrugsR01CA122814 · NCI · JOHNS HOPKINS UNIVERSITY · PI LIU, JUN O. · 2008 to 2012
$1.7M
Type I Diabetes Model in ZebrafishR41DK082060 · NIDDK · LUMINOMICS, INC. · PI SAXENA, MEERA T · 2009 to 2009
$196k
NCI NIH HHS P01 CA134292NCI NIH HHS P01CA134292NCI NIH HHS R01 CA122814NCI NIH HHS R01CA122814NIDDK NIH HHS P30 DK079637NIDDK NIH HHS R01 DK080730NIDDK NIH HHS R01DK080730NIDDK NIH HHS R41 DK082060NIDDK NIH HHS R41DK082060NIDDK NIH HHS RC4 DK090816
6 · The paper itself

Abstract

Pancreatic β-cells are an essential source of insulin and their destruction because of autoimmunity causes type I diabetes. We conducted a chemical screen to identify compounds that would induce the differentiation of insulin-producing β-cells in vivo. To do this screen, we brought together the use of transgenic zebrafish as a model of β-cell differentiation, a unique multiwell plate that allows easy visualization of lateral views of swimming larval fish and a library of clinical drugs. We identified six hits that can induce precocious differentiation of secondary islets in larval zebrafish. Three of these six hits were known drugs with a considerable background of published data on mechanism of action. Using pharmacological approaches, we have identified and characterized two unique pathways in β-cell differentiation in the zebrafish, including down-regulation of GTP production and retinoic acid biosynthesis.

Indexed as

AcetanilidesAnimalsAnimals, Genetically ModifiedCaffeic AcidsCell DifferentiationCell Line, TumorCell ProliferationDimethyl SulfoxideDNA PrimersDose-Response Relationship, DrugDrug DiscoveryEpirizoleFluorescent Antibody TechniqueGreen Fluorescent ProteinsGuanosine TriphosphateHMGB1 ProteinAcetanilidesCaffeic AcidsC.I. Solvent Yellow 56Dimethyl SulfoxideDNA PrimersEpirizoleGreen Fluorescent ProteinsGuanosine TriphosphateHMGB1 ProteinMycophenolic AcidN-(4-(3-(3,4-dihydroxyphenyl)acryloyl)phenyl)-2-(thiophen-2-yl)acetamidep-AminoazobenzenePharmaceutical PreparationsSulfanilic AcidsTretinoin

Identifiers

PMID22084084
PMCPMC3228434
OpenAlexW2151126374

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.