Evidence map›Paper›PMID 29986926›Full record

ArticleDiabetes2018

Restoration of Glucose-Stimulated Cdc42-Pak1 Activation and Insulin Secretion by a Selective Epac Activator in Type 2 Diabetic Human Islets.

Rajakrishnan Veluthakal, Oleg G Chepurny, Colin A Leech, Frank Schwede, George G Holz, Debbie C Thurmond

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  11. The adaptor protein APPL2 controls glucose-stimulated insulin secretion via F-actin remodeling in pancreatic β-cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
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  14. Metabolic regulation through the endosomal system.Traffic (Copenhagen, Denmark) · 2019
    Review
  15. Article
  16. Review
  17. Cyclic AMP-dependent protein kinase A and EPAC mediate VIP and secretin stimulation of PAK4 and activation of NaAmerican journal of physiology. Gastrointestinal and liver physiology · 2019
    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

6 authors at 3 institutions in 2 countries.

Rajakrishnan VeluthakalDepartment of Molecular and Cellular Endocrinology, Diabetes and Metabolism Research Institute, Beckman Research Institute of City of Hope, Duarte, CA rveluthakal@coh.org.ORCID 0000-0002-4685-0647
Oleg G ChepurnyDepartment of Medicine, State University of New York, Upstate Medical University, Syracuse, NY.
Colin A LeechDepartment of Medicine, State University of New York, Upstate Medical University, Syracuse, NY.
Frank SchwedeBIOLOG Life Science Institute, Bremen, Germany.
George G HolzDepartment of Medicine, State University of New York, Upstate Medical University, Syracuse, NY.
Debbie C ThurmondDepartment of Molecular and Cellular Endocrinology, Diabetes and Metabolism Research Institute, Beckman Research Institute of City of Hope, Duarte, CA.ORCID 0000-0002-6303-4596
SUNY Upstate Medical University · USCity of Hope · USBiolog Life Science Institute · DE

Funding

Regulation of Glucose Homeostasis by Munc18 ProteinsR01DK067912 · NIDDK · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI THURMOND, DEBBIE C · 2004 to 2023
$6.5M
Targeting PAK1 to improve functional beta-cell mass and insulin sensitivityR01DK102233 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI THURMOND, DEBBIE C, VELUTHAKAL, RAJAKRISHNAN · 2014 to 2024
$3.3M
Molecular Basis of Antidiabetogenic Hormone ActionR01DK069575 · NIDDK · UPSTATE MEDICAL UNIVERSITY · PI HOLZ, GEORGE G · 2007 to 2017
$2.9M
Alpha7 Nicotinic Acetylcholine Receptor Regulation of Glucagon-Like Peptide-1 Incretin Hormone Action.R01DK122332 · NIDDK · UPSTATE MEDICAL UNIVERSITY · PI HOLZ, GEORGE G · 2020 to 2023
$1.6M
NIDDK NIH HHS R01 DK067912NIDDK NIH HHS R01 DK069575NIDDK NIH HHS R01 DK102233NIDDK NIH HHS R01 DK122332
6 · The paper itself

Abstract

Glucose metabolism stimulates cell division control protein 42 homolog (Cdc42)-p21-activated kinase (Pak1) activity and initiates filamentous actin (F-actin) cytoskeleton remodeling in pancreatic β-cells so that cytoplasmic secretory granules can translocate to the plasma membrane where insulin exocytosis occurs. Since glucose metabolism also generates cAMP in β-cells, the cross talk of cAMP signaling with Cdc42-Pak1 activation might be of fundamental importance to glucose-stimulated insulin secretion (GSIS). Previously, the type-2 isoform of cAMP-regulated guanine nucleotide exchange factor 2 (Epac2) was established to mediate a potentiation of GSIS by cAMP-elevating agents. Here we report that nondiabetic human islets and INS-1 832/13 β-cells treated with the selective Epac activator 8-pCPT-2'-

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAnimalscdc42 GTP-Binding ProteinCell LineDiabetes Mellitus, Type 2GlucoseGuanine Nucleotide Exchange FactorsHumansInsulinInsulin-Secreting CellsInsulin SecretionIslets of Langerhansp21-Activated KinasesRatsThionucleotides8-bromoadenosine-3',5'-cyclic monophosphorothioate8-Bromo Cyclic Adenosine Monophosphatecdc42 GTP-Binding ProteinGlucoseGuanine Nucleotide Exchange FactorsInsulinp21-Activated KinasesRapgef4 protein, ratThionucleotides

Identifiers

PMID29986926
PMCPMC6152341
OpenAlexW2854536540

What Socratic 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 Socratic graph.