Evidence map›Paper›PMID 27105622›Full record

ReviewCellular and molecular life sciences : CMLS2016

A synopsis of factors regulating beta cell development and beta cell mass.

Krishna Prasadan, Chiyo Shiota, Xiao Xiangwei, David Ricks, Joseph Fusco, George Gittes

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Stem Cell Therapy for the Management of Type 1 Diabetes: Advances and Perspectives.Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. 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 2 institutions in 1 country.

Krishna PrasadanRangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Chiyo ShiotaRangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Xiao XiangweiRangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
David RicksRangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Joseph FuscoRangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
George GittesRangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA. gittesgk@upmc.edu.
University of Pittsburgh · USChildren's Hospital of Pittsburgh · US

Funding

TFG-Beta Isoform Signaling in Pancreatic DevelopmentR01DK058400 · NIDDK · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI GITTES, GEORGE K. · 2002 to 2004
$742k
Pancreatic Intra-Islet DuctsR01DK098196 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GITTES, GEORGE K. · 2013 to 2014
$667k
Glucagon family peptide signaling regulates pancreatic endocrine expansionR03HD080746 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PRASADAN, KRISHNA · 2014 to 2015
$152k
NICHD NIH HHS R03 HD080746NIDDK NIH HHS R01 DK058400NIDDK NIH HHS R01 DK098196
6 · The paper itself

Abstract

The insulin-secreting beta cells in the endocrine pancreas regulate blood glucose levels, and loss of functional beta cells leads to insulin deficiency, hyperglycemia (high blood glucose) and diabetes mellitus. Current treatment strategies for type-1 (autoimmune) diabetes are islet transplantation, which has significant risks and limitations, or normalization of blood glucose with insulin injections, which is clearly not ideal. The type-1 patients can lack insulin counter-regulatory mechanism; therefore, hypoglycemia is a potential risk. Hence, a cell-based therapy offers a better alternative for the treatment of diabetes. Past research was focused on attempting to generate replacement beta cells from stem cells; however, recently there has been an increasing interest in identifying mechanisms that will lead to the conversion of pre-existing differentiated endocrine cells into beta cells. The goal of this review is to provide an overview of several of the key factors that regulate new beta cell formation (neogenesis) and beta cell proliferation.

Indexed as

AnimalsHumansInsulin-Secreting CellsIntercellular Signaling Peptides and ProteinsOrgan SizeSignal TransductionTranscription FactorsTransforming Growth Factor betaIntercellular Signaling Peptides and ProteinsTranscription FactorsTransforming Growth Factor betaBeta cellGLP-1GlucagonProliferationRegenerationSmad7Vascular endothelial growth factor (VEGF)

Identifiers

PMID27105622
PMCPMC5002366
OpenAlexW2337987156

What OpenQuestion 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 OpenQuestion graph.