Evidence map›Paper›PMID 31676778›Full record

ArticleNature communications2019

Neratinib protects pancreatic beta cells in diabetes.

Amin Ardestani, Sijia Li, Karthika Annamalai, Blaz Lupse, Shirin Geravandi, Aleksandra Dobrowolski, Shan Yu, Siying Zhu, Tyler D Baguley, Murali Surakattula and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.7field-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

34 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  12. Future treatment of Diabetes - Tyrosine Kinase inhibitors.Journal of diabetes and metabolic disorders · 2023
    Review
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  14. Article
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  17. Article
  18. Article
  19. Article
  20. Apoptosis in Type 2 Diabetes: Can It Be Prevented? Hippo Pathway Prospects.International journal of molecular sciences · 2022
    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

23 authors at 3 institutions in 2 countries.

Amin ArdestaniCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany. ardestani.amin@gmail.com.
Sijia LiCalibr at Scripps Research, La Jolla, CA, USA.
Karthika AnnamalaiCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Blaz LupseCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Shirin GeravandiCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Aleksandra DobrowolskiCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Shan YuCalibr at Scripps Research, La Jolla, CA, USA.
Siying ZhuCalibr at Scripps Research, La Jolla, CA, USA.
Tyler D BaguleyCalibr at Scripps Research, La Jolla, CA, USA.
Murali SurakattulaCalibr at Scripps Research, La Jolla, CA, USA.
Janina OetjenCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.ORCID http://orcid.org/0000-0002-4088-5742
Lena Hauberg-LotteCenter for Industrial Mathematics, University of Bremen, Bremen, Germany.
Raquel HerranzCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Sushil AwalCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Delsi AltenhofenCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany.
Van Nguyen-TranCalibr at Scripps Research, La Jolla, CA, USA.
Sean JosephCalibr at Scripps Research, La Jolla, CA, USA.
Peter G SchultzCalibr at Scripps Research, La Jolla, CA, USA.
Arnab K ChatterjeeCalibr at Scripps Research, La Jolla, CA, USA.
Nikki RogersCalibr at Scripps Research, La Jolla, CA, USA.
Matthew S TremblayCalibr at Scripps Research, La Jolla, CA, USA. mtremblay@scripps.edu.
Weijun ShenCalibr at Scripps Research, La Jolla, CA, USA. wshen@scripps.edu.
Kathrin MaedlerCentre for Biomolecular Interactions Bremen, University of Bremen, Bremen, Germany. kmaedler@uni-bremen.de.ORCID http://orcid.org/0000-0002-7436-1197
University of Bremen · DEScripps Institution of Oceanography · USScripps Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The loss of functional insulin-producing β-cells is a hallmark of diabetes. Mammalian sterile 20-like kinase 1 (MST1) is a key regulator of pancreatic β-cell death and dysfunction; its deficiency restores functional β-cells and normoglycemia. The identification of MST1 inhibitors represents a promising approach for a β-cell-protective diabetes therapy. Here, we identify neratinib, an FDA-approved drug targeting HER2/EGFR dual kinases, as a potent MST1 inhibitor, which improves β-cell survival under multiple diabetogenic conditions in human islets and INS-1E cells. In a pre-clinical study, neratinib attenuates hyperglycemia and improves β-cell function, survival and β-cell mass in type 1 (streptozotocin) and type 2 (obese Lepr

Indexed as

AnimalsCell Line, TumorCells, CulturedDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Hippo KinasesHumansInsulin-Secreting CellsMaleMice, Inbred C57BLMice, ObeseProtective AgentsProtein Serine-Threonine KinasesQuinolinesRatsSignal TransductionHippo KinasesneratinibProtective AgentsProtein Serine-Threonine KinasesQuinolinesStk4 protein, mouse

Identifiers

PMID31676778
PMCPMC6825211
OpenAlexW2987638675

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.