Evidence map›Paper›PMID 40921827›Full record

ArticleScientific reports2025

MDM4 enables efficient human iPS cell generation from PBMCs using synthetic RNAs.

Masato Nakagawa, Mizuho Nogi, Hatsuki Doi, Ryuhei Hayashi, Tomohiko Katayama, Hirohisa Ohno, Megumi Mochizuki, Karin Hayashi, Hirohide Saito

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

9 authors.

Masato Nakagawa *Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan. nakagawa@cira.kyoto-u.ac.jp.
Mizuho Nogi *Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.
Hatsuki DoiCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.
Ryuhei HayashiDepartment of Ophthalmology, Graduate School of Medicine, The University of Osaka, Suita, Osaka, 565-0871, Japan.
Tomohiko KatayamaPremium Research Institute for Human Metaverse Medicine (WPI-PRIMe), The University of Osaka, Osaka, 565-0871, Japan.
Hirohisa OhnoCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.
Megumi MochizukiCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.
Karin HayashiCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.
Hirohide SaitoCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.

Funding

Fusion Oriented REsearch for disruptive Science and Technology JPMJFR210WJapan Agency for Medical Research and Development JP22bm0104001 and JP23bm1323001Japan Science and Technology Agency (JST), and a Grants-in-Aid for Scientific Research 23H03060 and 23K27751
6 · The paper itself

Abstract

If iPS cells can be established easily and efficiently using freshly collected blood cells, it will enhance regenerative and personalized medicine. While reports of iPS derivation from blood-derived endothelial progenitor cells using RNA have been documented, none have been reported from peripheral blood-derived mononuclear cells (PBMCs). In this study, we established a method to generate iPS cells from PBMCs using synthetic RNAs and found that MDM4, which suppresses p53, improved reprogramming efficiency.

Indexed as

Cell Cycle ProteinsInduced Pluripotent Stem CellsLeukocytes, MononuclearProto-Oncogene ProteinsRNACell DifferentiationCells, CulturedCellular ReprogrammingHumansTumor Suppressor Protein p53Cell Cycle ProteinsMDM4 protein, humanProto-Oncogene ProteinsRNATumor Suppressor Protein p53

Identifiers

PMID40921827
PMCPMC12417537

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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.