Evidence map›Paper›PMID 25028245›Full record

ReviewTrends in endocrinology and metabolism: TEM2014

Munc18c: a controversial regulator of peripheral insulin action.

Latha Ramalingam, Stephanie M Yoder, Eunjin Oh, Debbie C Thurmond

Open access · bronzeAbstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Cells · 2023
    Review
  3. Review
  4. Review
  5. Metabolic regulation through the endosomal system.Traffic (Copenhagen, Denmark) · 2019
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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

4 authors at 1 institution in 1 country.

Latha RamalingamDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Stephanie M YoderDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Eunjin OhDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Debbie C ThurmondDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN 46202, USA; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA; Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN 46202, USA. Electronic address: dthurmon@iu.edu.
Indiana University – Purdue University Indianapolis · US

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
Cdc42-regulated insulin granule exocytosisR01DK076614 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI THURMOND, DEBBIE C · 2008 to 2012
$1.6M
The Role of the Cdc42-Pak1 Signaling Pathway in the Incretin EffectF32DK094488 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI YODER, STEPHANIE MICHELLE · 2011 to 2013
$134k
NIDDK NIH HHS DK067912NIDDK NIH HHS DK094488NIDDK NIH HHS F32 DK094488NIDDK NIH HHS R01 DK067912NIDDK NIH HHS R01 DK076614NIDDK NIH HHS R01 DK102233
6 · The paper itself

Abstract

Insulin resistance, a hallmark of impaired glucose tolerance and type 2 diabetes (T2D), arises from dysfunction of insulin action and subsequent glucose uptake by peripheral tissues, predominantly skeletal muscle and fat. Exocytosis of glucose transporter (GLUT4)-containing vesicles facilitated by soluble NSF (N-ethylmaleimide-sensitive factor) attachment receptor (SNARE) protein isoforms, and Munc18c (mammalian homolog of Unc-18c) mediates this glucose uptake. Emerging evidences, including recent human clinical studies, point to pivotal roles for Munc18c in peripheral insulin action in adipose and skeletal muscle. Intriguing new advances are also initiating debates regarding the molecular mechanism(s) controlling Munc18c action. The objective of this review is therefore to present a balanced perspective of new continuities and controversies surrounding the regulation and requirement for Munc18c in the regulation of peripheral insulin action.

Indexed as

Adipose TissueAnimalsGlucoseHumansInsulinInsulin ResistanceMultiprotein ComplexesMunc18 ProteinsMuscle, SkeletalSNARE ProteinsGlucoseInsulinMultiprotein ComplexesMunc18 ProteinsSNARE Proteinsadiposeglucose uptakeGLUT4 vesicle exocytosisskeletal muscleSNARE proteins

Identifiers

PMID25028245
PMCPMC4253632
OpenAlexW2028759906

What Socratic holds

Textmetadata
LicenceTDM
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.