Evidence map›Paper›PMID 20595386›Full record

ArticleThe Journal of biological chemistry2010

Induction of pluripotent stem cells from human third molar mesenchymal stromal cells.

Yasuaki Oda, Yasuhide Yoshimura, Hiroe Ohnishi, Mika Tadokoro, Yoshihiro Katsube, Mari Sasao, Yoko Kubo, Koji Hattori, Shigeru Saito, Katsuhisa Horimoto and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
7.8field-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

52 citing papers in PubMed, 136 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Functional genomics in stem cell models: considerations and applications.Frontiers in cell and developmental biology · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Generation of Human-Induced Pluripotent Stem Cells From Anterior Cruciate Ligament.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Induced Pluripotent Stem (iPS) Cells in Dentistry: A Review.International journal of stem cells · 2016
    Review
  19. Techniques of Human Embryonic Stem Cell and Induced Pluripotent Stem Cell Derivation.Archivum immunologiae et therapiae experimentalis · 2016
    Review
  20. Induced pluripotent stem cells in dentistry.Journal of pharmacy & bioallied sciences · 2016
    Review
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

12 authors at 1 institution in 1 country.

Yasuaki OdaTissue Engineering Research Group, Health Research Institute, National Institute of Advanced Industrial Science and Technology, Hyogo 661-0974, Japan.
Yasuhide Yoshimura
Hiroe Ohnishi
Mika Tadokoro
Yoshihiro Katsube
Mari Sasao
Yoko Kubo
Koji Hattori
Shigeru Saito
Katsuhisa Horimoto
Shunsuke Yuba
Hajime Ohgushi
National Institute of Advanced Industrial Science and Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of four transcription factors (OCT3/4, SOX2, KLF4, and MYC) can reprogram mouse as well as human somatic cells to induced pluripotent stem (iPS) cells. We generated iPS cells from mesenchymal stromal cells (MSCs) derived from human third molars (wisdom teeth) by retroviral transduction of OCT3/4, SOX2, and KLF4 without MYC, which is considered as oncogene. Interestingly, some of the clonally expanded MSCs could be used for iPS cell generation with 30-100-fold higher efficiency when compared with that of other clonally expanded MSCs and human dermal fibroblasts. Global gene expression profiles demonstrated some up-regulated genes regarding DNA repair/histone conformational change in the efficient clones, suggesting that the processes of chromatin remodeling have important roles in the cascade of iPS cells generation. The generated iPS cells resembled human embryonic stem (ES) cells in many aspects, including morphology, ES marker expression, global gene expression, epigenetic states, and the ability to differentiate into the three germ layers in vitro and in vivo. Because human third molars are discarded as clinical waste, our data indicate that clonally expanded MSCs derived from human third molars are a valuable cell source for the generation of iPS cells.

Indexed as

AnimalsCell DifferentiationCells, CulturedHumansImmunohistochemistryInduced Pluripotent Stem CellsKaryotypingKruppel-Like Factor 4MiceOligonucleotide Array Sequence AnalysisStromal CellsToothKruppel-Like Factor 4

Identifiers

PMID20595386
PMCPMC2937959
OpenAlexW2016335094

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.