Evidence map›Paper›PMID 30286143›Full record

ArticlePloS one2018

Tumorigenicity-associated characteristics of human iPS cell lines.

Satoshi Yasuda, Shinji Kusakawa, Takuya Kuroda, Takumi Miura, Keiko Tano, Nozomi Takada, Satoko Matsuyama, Akifumi Matsuyama, Michiyo Nasu, Akihiro Umezawa and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

50 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
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  6. Review
  7. Personalized Stem Cell-Based Regeneration in Spinal Cord Injury Care.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Review
  10. Review
  11. Detection of Residual iPSCs Following Differentiation of iPSC-Derived Retinal Pigment Epithelial Cells.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
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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

13 authors at 6 institutions in 1 country.

Satoshi YasudaDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.ORCID 0000-0002-1011-0815
Shinji KusakawaDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.
Takuya KurodaDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.
Takumi MiuraDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.
Keiko TanoDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.
Nozomi TakadaCenter for Rare Disease Research, National Institute of Biomedical Innovation, Health and Nutrition, Osaka, Japan.
Satoko MatsuyamaDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.
Akifumi MatsuyamaCenter for Rare Disease Research, National Institute of Biomedical Innovation, Health and Nutrition, Osaka, Japan.
Michiyo NasuCenter for Regenerative Medicine, National Research Institute for Child Health and Development, Tokyo, Japan.
Akihiro UmezawaCenter for Regenerative Medicine, National Research Institute for Child Health and Development, Tokyo, Japan.
Takao HayakawaPharmaceutical Research and Technology Institute, Kindai University, Osaka, Japan.
Hideki TsutsumiCentral Institute for Experimental Animals, Kawasaki, Japan.
Yoji SatoDivision of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kawasaki, Japan.ORCID 0000-0002-9889-1272
National Institute of Health Sciences · JPNational Institute of Biomedical Innovation, Health and Nutrition · JPNational Center For Child Health and Development · JPCentral Institute for Experimental Animals · JPKindai University · JPKyushu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human induced pluripotent stem cells (hiPSCs) represent promising raw materials of human cell-based therapeutic products (hCTPs). As undifferentiated hiPSCs exhibit intrinsic tumorigenicity properties that enable them to form teratomas, hCTPs containing residual undifferentiated hiPSCs may cause tumor formation following transplantation. We first established quantitative and sensitive tumorigenicity testing of hiPSCs dissociated into single cells using NOD/Shi-scid IL2Rγnull (NOG) mice by inhibiting apoptosis of hiPSCs with a Rho kinase inhibitor. To examine different features in tumorigenicity of various hiPSCs, 10 commonly available hiPSC lines were subjected to in vivo tumorigenicity testing. Transplanted hiPSC lines showed remarkable variation in tumor incidence, formation latency, and volumes. Most of the tumors formed were classified as immature teratomas. However, no signs of malignancies, such as carcinoma and sarcoma, were recognized in the tumors. Characteristics associated tumorigenicity of hiPSCs were investigated with microarray analysis, karyotype analysis, and whole exome sequencing. Gene expression profiling and pathway analysis supported different features of hiPSC lines in tumorigenicity. hiPSC lines showed chromosomal abnormalities in some lines and 61-77 variants of cancer-related genes carrying effective nonsynonymous mutations, which were confirmed in the COSMIC databases. In this study, the chromosomal abnormalities and cancer-related gene mutations observed in hiPSC lines did not lead to the malignancy of tumors derived from hiPSCs. Our results suggest that the potential tumorigenicity risk of hCTPs containing residual undifferentiated hiPSCs is dependent on not only amounts of undifferentiated hiPSCs but also features of the cell lines used as raw materials, a finding that should be considered from the perspective of quality of hCTPs used.

Indexed as

CarcinogenesisCell LineExomeHumansInduced Pluripotent Stem CellsKaryotypeTranscriptome

Identifiers

PMID30286143
PMCPMC6171902
OpenAlexW2894849432

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.