Evidence map›Paper›PMID 22965062›Full record

ReviewNature biotechnology2012

Lessons from human teratomas to guide development of safe stem cell therapies.

Justine J Cunningham, Thomas M Ulbright, Martin F Pera, Leendert H J Looijenga

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature biotechnology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 184 citations in OpenAlex.

  1. Article
  2. Review
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  7. Frontiers in cell and developmental biology · 2024
    Review
  8. Salivary Gland Bioengineering.Bioengineering (Basel, Switzerland) · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
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  18. The Tumorigenic Potential of Human Pluripotent Stem Cells.Stem cells translational medicine · 2022
    Article
  19. Article
  20. Article

38 more citing papers are in PubMed but not listed here.

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

4 authors at 4 institutions in 4 countries.

Justine J CunninghamDepartment of Drug Safety Evaluation, Allergan Inc., Irvine, California, USA. cunningham_justine@allergan.com
Thomas M Ulbright
Martin F Pera
Leendert H J Looijenga
Allergan (United States) · USErasmus MC Cancer Institute · NLIndiana University – Purdue University Indianapolis · USUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The potential for the formation of teratomas or other neoplasms is a major safety roadblock to clinical application of pluripotent stem cell therapies. Preclinical assessment of the risk of tumor formation in this context poses considerable scientific and regulatory challenges, especially because animal xenograft models may not properly reflect the long-term tumorigenic potential of human cells. A better understanding of the biology of spontaneously occurring teratomas and related tumors in humans can help to guide efforts to assess and minimize the potential hazards of embryonic stem cell or induced pluripotent stem cell therapeutics. Here we review the features of teratomas derived experimentally from human pluripotent stem cells and argue that they most closely resemble spontaneous benign teratomas that occur early in both mouse and human life. The natural history and pathology of these spontaneously occurring teratomas provide important clues for preclinical safety assessment and patient monitoring in trials of stem cell therapies.

Indexed as

AnimalsFemaleHumansMaleMicePluripotent Stem CellsStem Cell TransplantationTeratoma

Identifiers

PMID22965062
OpenAlexW2058068800

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.