Evidence map›Paper›PMID 26561805›Full record

ReviewInternational journal of molecular sciences2015

Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced-Pluripotent Stem Cells.

Taku Kaitsuka, Kazuhito Tomizawa

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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
–field-weighted citation impact
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.

  1. 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

2 authors.

Taku KaitsukaDepartment of Molecular Physiology, Faculty of Life Sciences, Kumamoto University, 1-1-1 Honjyo, Kumamoto 860-8556, Japan. kaitsuka@kumamoto-u.ac.jp.
Kazuhito TomizawaDepartment of Molecular Physiology, Faculty of Life Sciences, Kumamoto University, 1-1-1 Honjyo, Kumamoto 860-8556, Japan. tomikt@kumamoto-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein transduction using cell-penetrating peptides (CPPs) is useful for the delivery of large protein molecules, including some transcription factors. This method is safer than gene transfection methods with a viral vector because there is no risk of genomic integration of the exogenous DNA. Recently, this method was reported as a means for the induction of induced pluripotent stem (iPS) cells, directing the differentiation into specific cell types and supporting gene editing/correction. Furthermore, we developed a direct differentiation method to obtain a pancreatic lineage from mouse and human pluripotent stem cells via the protein transduction of three transcription factors, Pdx1, NeuroD, and MafA. Here, we discuss the possibility of using CPPs as a means of directing the differentiation of iPS cells and other stem cell technologies.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell-Penetrating PeptidesCellular ReprogrammingCinnamatesGene ExpressionGlucagon-Like Peptide 1Homeodomain ProteinsHumansInduced Pluripotent Stem CellsInsulin-Secreting CellsIntercellular Signaling Peptides and ProteinsMaf Transcription Factors, LargeMiceNerve Tissue Proteins3-keto-N-aminoethylaminoethylcaproyldihydrocinnamoyl cyclopamineBasic Helix-Loop-Helix ProteinsCell-Penetrating PeptidesCinnamatesGlucagon-Like Peptide 1Homeodomain ProteinsIntercellular Signaling Peptides and ProteinsMAFA protein, humanMaf Transcription Factors, LargeNerve Tissue ProteinsNeurogenic differentiation factor 1Niacinamidepancreatic and duodenal homeobox 1 proteinTrans-ActivatorsTretinoinVeratrum Alkaloidscell-penetrating peptideinduced pluripotent stem cellpancreatic differentiationpoly-arginineprotein transduction

Identifiers

PMID26561805
PMCPMC4661845

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Registered trials

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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.