Evidence map›Paper›PMID 39626675›Full record

ArticleCell reports. Medicine2024

Cycling alpha cells in regenerative drug-treated human pancreatic islets may serve as key beta cell progenitors.

Esra Karakose, Xuedi Wang, Peng Wang, Saul Carcamo, Deniz Demircioglu, Luca Lambertini, Olivia Wood, Randy Kang, Geming Lu, Donald K Scott and 5 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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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

15 authors.

Esra KarakoseDiabetes, Obesity, Metabolism Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: esra.karakose@mssm.edu.
Xuedi WangTisch Cancer Institute Bioinformatics for Next Generation Sequencing (BiNGS) Core, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Peng WangDiabetes, Obesity, Metabolism Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Saul CarcamoTisch Cancer Institute Bioinformatics for Next Generation Sequencing (BiNGS) Core, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Deniz DemirciogluTisch Cancer Institute Bioinformatics for Next Generation Sequencing (BiNGS) Core, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Luca LambertiniDiabetes, Obesity, Metabolism Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Olivia WoodDiabetes, Obesity, Metabolism Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Randy KangDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Geming LuDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Donald K ScottDiabetes, Obesity, Metabolism Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Adolfo Garcia-OcañaDepartment of Molecular and Cellular Endocrinology, Arthur Riggs Diabetes and Metabolism Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Carmen ArgmannDepartment of Genetics and Genomic Sciences, The Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Robert P SebraDepartment of Genetics and Genomic Sciences, The Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Dan HassonTisch Cancer Institute Bioinformatics for Next Generation Sequencing (BiNGS) Core, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Andrew F StewartDiabetes, Obesity, Metabolism Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Funding

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
DREAM Complex Maintenance of Human Beta Cell QuiescenceR01DK129196 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI STEWART, ANDREW F., WANG, PENG · 2021 to 2025
$3.0M
Biological and Medicinal Chemistry Approaches to Human Beta Cell RegenerationR01DK125285 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DEVITA, ROBERT J, GARCIA-OCANA, ADOLFO · 2020 to 2023
$2.5M
COVID and Translational Science supercomputer (CATS)S10OD030463 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2021 to 2021
$2.0M
Epigenetic regulation in therapeutic human pancreatic beta cell proliferationK01DK128378 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KARAKOSE-BALIOGLU, ESRA · 2021 to 2024
$607k
NIDDK NIH HHS K01 DK128378NIDDK NIH HHS R01 DK105015NIDDK NIH HHS R01 DK125285NIDDK NIH HHS R01 DK129196NIH HHS S10 OD030463
6 · The paper itself

Abstract

Diabetes results from an inadequate number of insulin-producing human beta cells. There is currently no clinically available effective means to restore beta cell mass in millions of people with diabetes. Although the DYRK1A inhibitors, either alone or in combination with GLP-1 receptor agonists (GLP-1) or transforming growth factor β (TGF-β) superfamily inhibitors (LY), induce beta cell replication and increase beta cell mass, the precise mechanisms of action remain elusive. Here we perform single-cell RNA sequencing on human pancreatic islets treated with a DYRK1A inhibitor, either alone or with GLP-1 or LY. We identify cycling alpha cells as the most responsive cells to DYRK1A inhibition. Lineage trajectory analyses suggest that cycling alpha cells may serve as precursor cells that transdifferentiate into beta cells. Collectively, in addition to enhancing expression of beta cell phenotypic genes in beta cells, our findings suggest that regenerative drugs may be targeting cycling alpha cells in human islets.

Indexed as

Dyrk KinasesGlucagon-Secreting CellsInsulin-Secreting CellsCell CycleCell TransdifferentiationGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorHumansIslets of LangerhansProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRegenerationStem CellsTransforming Growth Factor betaDyrk KinasesGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorProtein Serine-Threonine KinasesProtein-Tyrosine KinasesTransforming Growth Factor betaalpha cellsbeta cellsdiabetesharminepancreatic isletsregenerationtransdifferentiation

Identifiers

PMID39626675
PMCPMC11722108

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Registered trials

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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.