Evidence map›Paper›PMID 26584542›Full record

ArticleStem cell reports2015

Repair of Ischemic Injury by Pluripotent Stem Cell Based Cell Therapy without Teratoma through Selective Photosensitivity.

Seung-Ju Cho, So-Yeon Kim, Ho-Chang Jeong, Hyeonsik Cheong, Doseok Kim, Soon-Jung Park, Jong-Jin Choi, Hyongbum Kim, Hyung-Min Chung, Sung-Hwan Moon and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Deciphering theFrontiers in cell and developmental biology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Induced Pluripotent Stem (iPS) Cells in Dentistry: A Review.International journal of stem cells · 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

11 authors at 3 institutions in 1 country.

Seung-Ju ChoDepartment of Life Sciences, College of Natural Sciences, Sogang University, Seoul 121-742, Korea.
So-Yeon KimDepartment of Life Sciences, College of Natural Sciences, Sogang University, Seoul 121-742, Korea.
Ho-Chang JeongDepartment of Life Sciences, College of Natural Sciences, Sogang University, Seoul 121-742, Korea.
Hyeonsik CheongDepartment of Physics, College of Natural Sciences, Sogang University, Seoul 121-742, Korea.
Doseok KimDepartment of Physics, College of Natural Sciences, Sogang University, Seoul 121-742, Korea.
Soon-Jung ParkDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul 143-701, Korea.
Jong-Jin ChoiDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul 143-701, Korea.
Hyongbum KimGraduate School of Biomedical Science and Engineering, College of Medicine, Hanyang University, Seoul 133-791, Korea.
Hyung-Min ChungDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul 143-701, Korea.
Sung-Hwan MoonDepartment of Medicine, School of Medicine, Konkuk University, Seoul 143-701, Korea. Electronic address: sunghwanmoon@kku.ac.kr.
Hyuk-Jin ChaDepartment of Life Sciences, College of Natural Sciences, Sogang University, Seoul 121-742, Korea. Electronic address: hjcha@sogang.ac.kr.
Sogang University · KRKonkuk University · KRHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem-toxic small molecules have been developed to induce selective cell death of pluripotent stem cells (PSCs) to lower the risk of teratoma formation. However, despite their high efficacies, chemical-based approaches may carry unexpected toxicities on specific differentiated cell types. Herein, we took advantage of KillerRed (KR) as a suicide gene, to selectively induce phototoxicity using visible light via the production of reactive oxygen species. PSCs in an undifferentiated state that exclusively expressed KR (KR-PSCs) were eliminated by a single exposure to visible light. This highly selective cell death in KR-PSCs was exploited to successfully inhibit teratoma formation. In particular, endothelial cells from KR-mPSCs remained fully functional in vitro and sufficient to repair ischemic injury in vivo regardless of light exposure, suggesting that a genetic approach in which KR is expressed in a tightly controlled manner would be a viable strategy to inhibit teratoma formation for future safe PSC-based therapies.

Indexed as

AnimalsCell- and Tissue-Based TherapyCell DeathCell DifferentiationEndothelial CellsFemaleHindlimbIschemiaLightMiceMice, NudePluripotent Stem CellsReactive Oxygen SpeciesTeratomaReactive Oxygen Speciesischemic injuryKillerRedphototoxicitypluripotent stem cellsteratomavasculogenesis

Identifiers

PMID26584542
PMCPMC4682089
OpenAlexW2174678419

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.