Evidence map›Paper›PMID 34722569›Full record

ReviewFrontiers in medicine2021

iPSC-Derived Organoids as Therapeutic Models in Regenerative Medicine and Oncology.

Ali G Turhan, Jinwook W Hwang, Diana Chaker, Albert Tasteyre, Theodoros Latsis, Frank Griscelli, Christophe Desterke, Annelise Bennaceur-Griscelli

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  16. Article
  17. Engineered organoids for biomedical applications.Advanced drug delivery reviews · 2023
    Review
  18. Review
  19. Article
  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

8 authors at 3 institutions in 1 country.

Ali G TurhanINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Jinwook W HwangINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Diana ChakerINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Albert TasteyreINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Theodoros LatsisINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Frank GriscelliINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Christophe DesterkeINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Annelise Bennaceur-GriscelliINSERM UA/09 UMR-S 935, Université Paris Saclay, Villejuif, France.
Inserm · FRGenopole (France) · FRLaboratoire d'études sur les monothéismes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progress made during the last decade in stem cell biology allows currently an unprecedented potential to translate these advances into the clinical applications and to shape the future of regenerative medicine. Organoid technology is amongst these major developments, derived from primary tissues or more recently, from induced pluripotent stem cells (iPSC). The use of iPSC technology offers the possibility of cancer modeling especially in hereditary cancers with germline oncogenic mutations. Similarly, it has the advantage to be amenable to genome editing with introduction of specific oncogenic alterations using CRISPR-mediated gene editing. In the field of regenerative medicine, iPSC-derived organoids hold promise for the generation of future advanced therapeutic medicinal products (ATMP) for organ repair. Finally, it appears that they can be of highly useful experimental tools to determine cell targets of SARS-Cov-2 infections allowing to test anti-Covid drugs. Thus, with the possibilities of genomic editing and the development of new protocols for differentiation toward functional tissues, it is expected that iPSC-derived organoid technology will represent also a therapeutic tool in all areas of medicine.

Indexed as

cancerdrug discoveryinduced pluripotent stem (IPS) cellorganoidregenerative medicine

Identifiers

PMID34722569
PMCPMC8548367
OpenAlexW3206198133

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.