Evidence map›Paper›PMID 26696512›Full record

ReviewBest practice & research. Clinical endocrinology & metabolism2015

Proper activation of MafA is required for optimal differentiation and maturation of pancreatic β-cells.

Ilham El Khattabi, Arun Sharma

Abstract readReview
In one paragraph

Review in Best practice & research. Clinical endocrinology & metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  5. Exendin-4 enhances insulin-positive phenotype of human pluripotent stem cell-derived β cells during transplantation.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
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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

2 authors at 1 institution in 1 country.

Ilham El KhattabiJoslin Diabetes Center, One Joslin Place, Boston, MA 02215, USA. Electronic address: elkhattabilham@gmail.com.
Arun SharmaCardiovascular and Metabolic Diseases, MedImmune, Gaithersburg, MD 20878, USA. Electronic address: sharmaar@medimmune.com.
Joslin Diabetes Center · US

Funding

RIPE3b1, An Important Insulin Gene Transcription FactorR01DK060127 · NIDDK · JOSLIN DIABETES CENTER · PI SHARMA, ARUN J · 2003 to 2010
$2.5M
NIDDK NIH HHS R01 DK060127NIDDK NIH HHS R01DK06127
6 · The paper itself

Abstract

A key therapeutic approach for the treatment of Type 1 diabetes (T1D) is transplantation of functional islet β-cells. Despite recent advances in generating stem cell-derived glucose-responsive insulin(+) cells, their further maturation to fully functional adult β-cells still remains a daunting task. Conquering this hurdle will require a better understanding of the mechanisms driving maturation of embryonic insulin(+) cells into adult β-cells, and the implementation of that knowledge to improve current differentiation protocols. Here, we will review our current understanding of β-cell maturation, and discuss the contribution of key β-cell transcription factor MafA, to this process. The fundamental importance of MafA in regulating adult β-cell maturation and function indicates that enhancing MafA expression may improve the generation of definitive β-cells for transplantation. Additionally, we suggest that the temporal control of MafA induction at a specific stage of β-cell differentiation will be the next critical challenge for achieving optimum maturation of β-cells.

Indexed as

Cell DifferentiationAnimalsHumansInsulin-Secreting CellsMaf Transcription Factors, LargeMaf Transcription Factors, Largeinsulin transcription factorMafAstem cell differentiationβ-cell differentiationβ-cell maturationβ-cells

Identifiers

PMID26696512
PMCPMC4690007
OpenAlexW1885748848

What OpenQuestion holds

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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.