Evidence map›Paper›PMID 35562869›Full record

ReviewInternational journal of molecular sciences2022

Role of the Transcription Factor MAFA in the Maintenance of Pancreatic β-Cells.

Wataru Nishimura, Hiroaki Iwasa, Munkhtuya Tumurkhuu

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

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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

3 authors at 3 institutions in 2 countries.

Wataru NishimuraDepartment of Molecular Biology, School of Medicine, International University of Health and Welfare, Narita 286-8686, Chiba, Japan.ORCID 0000-0002-8068-1277
Hiroaki IwasaDepartment of Molecular Biology, School of Medicine, International University of Health and Welfare, Narita 286-8686, Chiba, Japan.
Munkhtuya TumurkhuuDepartment of Genetics and Molecular Biology, School of Bio-Medicine, Mongolian National University of Medical Sciences, Ulaanbaatar 14210, Mongolia.
International University of Health and Welfare · JPJichi Medical University · JPMongolian National University · MN

Funding

International University of Health and Welfare n/aJapan Diabetes Foundation n/aJapan Eli Lilly n/aJapan Society for the Promotion of Science JP17K09843Japan Society for the Promotion of Science JP20K08915Teijin Pharma n/a
6 · The paper itself

Abstract

Pancreatic β-cells are specialized to properly regulate blood glucose. Maintenance of the mature β-cell phenotype is critical for glucose metabolism, and β-cell failure results in diabetes mellitus. Recent studies provide strong evidence that the mature phenotype of β-cells is maintained by several transcription factors. These factors are also required for β-cell differentiation from endocrine precursors or maturation from immature β-cells during pancreatic development. Because the reduction or loss of these factors leads to β-cell failure and diabetes, inducing the upregulation or inhibiting downregulation of these transcription factors would be beneficial for studies in both diabetes and stem cell biology. Here, we discuss one such factor, i.e., the transcription factor MAFA. MAFA is a basic leucine zipper family transcription factor that can activate the expression of insulin in β-cells with PDX1 and NEUROD1. MAFA is indeed indispensable for the maintenance of not only insulin expression but also function of adult β-cells. With loss of MAFA in type 2 diabetes, β-cells cannot maintain their mature phenotype and are dedifferentiated. In this review, we first briefly summarize the functional roles of MAFA in β-cells and then mainly focus on the molecular mechanism of cell fate conversion regulated by MAFA.

Indexed as

Diabetes Mellitus, Type 2Insulin-Secreting CellsCell DifferentiationHumansInsulinMaf Transcription Factors, LargeInsulinMaf Transcription Factors, Largededifferentiationdiabetes mellitusinsulinMAFAMAFBplasticitytranscription factorβ-cells

Identifiers

PMID35562869
PMCPMC9101179
OpenAlexW4224281065

What OpenQuestion holds

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LicenceCC BY
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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.