Evidence map›Paper›PMID 30485733›Full record

ArticleStem cells translational medicine2019

Selective Ablation of Tumorigenic Cells Following Human Induced Pluripotent Stem Cell-Derived Neural Stem/Progenitor Cell Transplantation in Spinal Cord Injury.

Kota Kojima, Hiroyuki Miyoshi, Narihito Nagoshi, Jun Kohyama, Go Itakura, Soya Kawabata, Masahiro Ozaki, Tsuyoshi Iida, Keiko Sugai, Shuhei Ito and 7 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

51 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Induced Pluripotent Stem Cells for Tissue-Engineered Skeletal Muscles.International journal of molecular sciences · 2023
    Review
  17. Review
  18. Article
  19. Review
  20. 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

17 authors at 2 institutions in 1 country.

Kota KojimaDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Hiroyuki MiyoshiDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Narihito NagoshiDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Jun KohyamaDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Go ItakuraDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Soya KawabataDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Masahiro OzakiDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Tsuyoshi IidaDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Keiko SugaiDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Shuhei ItoDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Ryuji FukuzawaDepartment of Pathology, International University of Health and Welfare, Chiba, Japan.
Kaori YasutakeDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Francois Renault-MiharaDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Shinsuke ShibataDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Morio MatsumotoDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Masaya NakamuraDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Hideyuki OkanoDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0001-7482-5935
Keio University · JPInternational University of Health and Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumorigenesis is an important problem that needs to be addressed in the field of human stem/progenitor cell transplantation for the treatment of subacute spinal cord injury (SCI). When certain "tumorigenic" cell lines are transplanted into the spinal cord of SCI mice model, there is initial improvement of motor function, followed by abrupt deterioration secondary to the effect of tumor growth. A significant proportion of the transplanted cells remains undifferentiated after transplantation and is thought to increase the risk of tumorigenesis. In this study, using lentiviral vectors, we introduced the herpes simplex virus type 1 thymidine kinase (HSVtk) gene into a human induced pluripotent stem cell-derived neural stem/progenitor cell (hiPSC-NS/PC) line that is known to undergo tumorigenic transformation. Such approach enables selective ablation of the immature proliferating cells and thereby prevents subsequent tumor formation. In vitro, the HSVtk system successfully ablated the immature proliferative neural cells while preserving mature postmitotic neuronal cells. Similar results were observed in vivo following transplantation into the injured spinal cords of immune-deficient (nonobese diabetic-severe combined immune-deficient) mice. Ablation of the proliferating cells exerted a protective effect on the motor function which was regained after transplantation, simultaneously defending the spinal cord from the harmful tumor growth. These results suggest a potentially promising role of suicide genes in opposing tumorigenesis during stem cell therapy. This system allows both preventing and treating tumorigenesis following hiPSC-NS/PC transplantation without sacrificing the improved motor function. Stem Cells Translational Medicine 2019;8:260&270.

Indexed as

AnimalsCarcinogenesisCell DifferentiationCells, CulturedDisease Models, AnimalFemaleHumansInduced Pluripotent Stem CellsMiceMice, Inbred NODMice, SCIDNeural Stem CellsNeuronsRecovery of FunctionSpinal CordSpinal Cord InjuriesHerpes simplex virus thymidine kinaseHuman induced pluripotent stem cell-derived neural stem/progenitor cellSpinal cord injuryStem cell therapySuicide gene

Identifiers

PMID30485733
PMCPMC6392358
OpenAlexW2902446331

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.