Evidence map›Paper›PMID 27624103›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2016

Development of a reliable automated screening system to identify small molecules and biologics that promote human β-cell regeneration.

Kristie I Aamodt, Radhika Aramandla, Judy J Brown, Nathalie Fiaschi-Taesch, Peng Wang, Andrew F Stewart, Marcela Brissova, Alvin C Powers

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2016. 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
3.5field-weighted citation impact, top 8% 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, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Scaling Insulin-Producing Cells by Multiple Strategies.Endocrinology and metabolism (Seoul, Korea) · 2024
    Review
  6. Article
  7. Article
  8. Small-molecule discovery in the pancreatic beta cell.Current opinion in chemical biology · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Islet Regeneration: Endogenous and Exogenous Approaches.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Review
  16. Role of Phosphodiesterase in the Biology and Pathology of Diabetes.International journal of molecular sciences · 2020
    Review
  17. Article
  18. Pancreatic β cell regeneration: To β or not to β.Current opinion in physiology · 2020
    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

8 authors at 2 institutions in 1 country.

Kristie I AamodtDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee.
Radhika AramandlaDivision of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Judy J BrownDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.
Nathalie Fiaschi-TaeschDivision of Endocrinology, Diabetes, and Bone Disease, Department of Medicine, Mount Sinai Medical Center, New York, New York; and.
Peng WangDivision of Endocrinology, Diabetes, and Bone Disease, Department of Medicine, Mount Sinai Medical Center, New York, New York; and.
Andrew F StewartDivision of Endocrinology, Diabetes, and Bone Disease, Department of Medicine, Mount Sinai Medical Center, New York, New York; and.
Marcela BrissovaDivision of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; marcela.brissova@vanderbilt.edu.
Alvin C PowersDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee.
Vanderbilt University Medical Center · USMount Sinai Medical Center · US

Funding

Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI JILL CRANDALL · 2015 to 2026
$27.7M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Discovery of Pancreatic Signatures in Type 2 Diabetes MellitusR24DK106755 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CAI, LONG, CAPRIOLI, RICHARD M · 2015 to 2019
$6.2M
DYRK Inhibitors for Human Beta Cell ExpansionR01DK105015 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DEVITA, ROBERT J, GARCIA-OCANA, ADOLFO · 2016 to 2024
$4.9M
Molecular Mechanisms of Physiologic Beta Cell Growth in Juvenile Human PancreasUC4DK104211 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIM, SEUNG K, POWERS, ALVIN C · 2014 to 2015
$4.0M
LSM880-Airyscan Confocal Microscope for Large Shared ResourceS10OD021630 · OD · VANDERBILT UNIVERSITY · PI WELLS, K. SAM · 2016 to 2016
$560k
Recruitment of bone marrow-derived cells required for beta cell regenerationF30DK097921 · NIDDK · VANDERBILT UNIVERSITY · PI AAMODT, KRISTIE · 2012 to 2015
$120k
NIDDK NIH HHS F30 DK097921NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK020593NIDDK NIH HHS R01 DK105015NIDDK NIH HHS R24 DK106755NIDDK NIH HHS UC4 DK104211NIGMS NIH HHS T32 GM007347NIH HHS S10 OD021630
6 · The paper itself

Abstract

Numerous compounds stimulate rodent β-cell proliferation; however, translating these findings to human β-cells remains a challenge. To examine human β-cell proliferation in response to such compounds, we developed a medium-throughput in vitro method of quantifying adult human β-cell proliferation markers. This method is based on high-content imaging of dispersed islet cells seeded in 384-well plates and automated cell counting that identifies fluorescently labeled β-cells with high specificity using both nuclear and cytoplasmic markers. β-Cells from each donor were assessed for their function and ability to enter the cell cycle by cotransduction with adenoviruses encoding cell cycle regulators cdk6 and cyclin D3. Using this approach, we tested 12 previously identified mitogens, including neurotransmitters, hormones, growth factors, and molecules, involved in adenosine and Tgf-1β signaling. Each compound was tested in a wide concentration range either in the presence of basal (5 mM) or high (11 mM) glucose. Treatment with the control compound harmine, a Dyrk1a inhibitor, led to a significant increase in Ki-67

Indexed as

ActivinsAdenosineAdenosine-5'-(N-ethylcarboxamide)Adenosine A2 Receptor AgonistsAdultAutomationCell Culture TechniquesCell ProliferationDrug Evaluation, PreclinicalErythropoietinExenatideFemaleGABA Agentsgamma-Aminobutyric AcidHarmineHumansA 134974activin AActivinsAdenosineAdenosine-5'-(N-ethylcarboxamide)Adenosine A2 Receptor AgonistsErythropoietinExenatideGABA Agentsgamma-Aminobutyric AcidHarmineIncretinsMonoamine Oxidase InhibitorsMyostatinNucleosidesPeptidesPlatelet-Derived Growth FactorProlactinSerotoninSerotonin Receptor AgonistsUK-432097Vasodilator AgentsVenomshuman isletβ-cell proliferation

Identifiers

PMID27624103
PMCPMC5130356
OpenAlexW2518918481

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.