Evidence map›Paper›PMID 28360105›Full record

ArticleThe Journal of biological chemistry2017

Demethylation of induced pluripotent stem cells from type 1 diabetic patients enhances differentiation into functional pancreatic β cells.

Gohar S Manzar, Eun-Mi Kim, Nicholas Zavazava

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

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  9. Organoids.Nature reviews. Methods primers · 2022
    Article
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  13. Modeling different types of diabetes using human pluripotent stem cells.Cellular and molecular life sciences : CMLS · 2021
    Review
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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 2 institutions in 2 countries.

Gohar S ManzarFrom the Department of Internal Medicine and University of Iowa, Iowa City, Iowa; Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa; Veterans Affairs Medical Center, Iowa City, Iowa,; Mayo Clinic College of Medicine, Rochester, Minnesota, and Daejeon 34114, Republic of Korea.
Eun-Mi KimFrom the Department of Internal Medicine and University of Iowa, Iowa City, Iowa; Veterans Affairs Medical Center, Iowa City, Iowa,; Predictive Model Research Center, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
Nicholas ZavazavaFrom the Department of Internal Medicine and University of Iowa, Iowa City, Iowa; Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa; Veterans Affairs Medical Center, Iowa City, Iowa,. Electronic address: nicholas-zavazava@uiowa.edu.
University of Iowa · USMayo Clinic · US

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Amy Leanne Ryan · 1998 to 2026
$30.5M
EMBRYONIC STEM CELLS INDUCE SPECIFIC GRAFT TOLERANCER01HL073015 · NHLBI · UNIVERSITY OF IOWA · PI ZAVAZAVA, NICHOLAS · 2004 to 2012
$2.5M
NHLBI NIH HHS R01 HL073015NIDDK NIH HHS P30 DK054759
6 · The paper itself

Abstract

Type 1 diabetes (T1D) can be managed by transplanting either the whole pancreas or isolated pancreatic islets. However, cadaveric pancreas is scarcely available for clinical use, limiting this approach. As such, there is a great need to identify alternative sources of clinically usable pancreatic tissues. Here, we used induced pluripotent stem (iPS) cells derived from patients with T1D to generate glucose-responsive, insulin-producing cells (IPCs) via 3D culture. Initially, T1D iPS cells were resistant to differentiation, but transient demethylation treatment significantly enhanced IPC yield. The cells responded to high-glucose stimulation by secreting insulin

Indexed as

AnimalsAzacitidineCadaverCell DifferentiationCells, CulturedDecitabineDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1DNA MethylationDNA Modification MethylasesEnzyme InhibitorsHumansHyperglycemiaInduced Pluripotent Stem CellsInsulinInsulin-Secreting CellsAzacitidineDecitabineDNA Modification MethylasesEnzyme InhibitorsInsulin3D differentiationbeta cellcell differentiationdiabetesinduced pluripotent stem cellinsulin producing cellsinsulin secretioniPSCiPS cellpancreatic islettype 1 diabetes

Identifiers

PMID28360105
PMCPMC5572901
OpenAlexW2603685462

What OpenQuestion 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 OpenQuestion graph.