Evidence map›Paper›PMID 34614263›Full record

ReviewTransplant international : official journal of the European Society for Organ Transplantation2021

Organoid transplant approaches for the liver.

Hasan Al Reza, Ryo Okabe, Takanori Takebe

Abstract readReview
In one paragraph

Review in Transplant international : official journal of the European Society for Organ Transplantation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Biomedical applications of organoids derived from the digestive system.Frontiers in cell and developmental biology · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. iPSC-derived cells for whole liver bioengineering.Frontiers in bioengineering and biotechnology · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Liver organoid culture methods.Cell & bioscience · 2023
    Review
  17. Article
  18. Review
  19. Review
  20. Article
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

3 authors.

Hasan Al RezaDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Ryo OkabeInstitute of Research, Tokyo Medical and Dental University, Tokyo, Japan.
Takanori TakebeDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
Modeling diabetes using an integrated plate systemUH3DK119982 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI LEE, MOO-YEAL, WELLS, JAMES M · 2020 to 2022
$5.4M
Engineering multi-organs in a dishDP2DK128799 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI TAKEBE, TAKANORI · 2020 to 2020
$2.3M
Modeling diabetes using an integrated plate systemUG3DK119982 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI LEE, MOO-YEAL, WELLS, JAMES M · 2018 to 2019
$1.7M
Cincinnati Children's Research FoundationCREST 20gm1210012h0001Dr. Ralph and Marian Falk Medical Research TrustFalk Catalyst Research Awards ProgramJapan Agency for Medical Research and Development JP18bm0704025h0001Japan Agency for Medical Research and Development JP18fk0210037h0001Japan Agency for Medical Research and Development JP21bm0404045h0003Japan Agency for Medical Research and Development JP21fk0210060h0003Japan Agency for Medical Research and Development JP21gm1210012h0002JSPS KAKENHI 19K22416JSPS KAKENHI JP18H02800JST Moonshot JPMJMS2022-10JST Moonshot JPMJMS2033-12Mitsubishi Foundation AwardNIDDK NIH HHS DP2 DK128799NIDDK NIH HHS P30 DK078392NIDDK NIH HHS UG3 DK119982NIDDK NIH HHS UH3 DK119982NIH Director's New Innovator Award DP2 DK128799-01NIH Director's New Innovator Award UG3/UH3 DK119982Takeda Science Foundation Award
6 · The paper itself

Abstract

Organoid technology is a state-of-the-art cell culture tool that has revolutionized study of development, regeneration, and diseases. Human liver organoids (HLOs) are now derived from either adult stem/progenitors or pluripotent stem cells (PSCs), emulating cellular diversity and structural symphony akin to the human liver. With the rapid rise in decompensated liver disease conditions only treated by liver transplant therapy, HLOs represent an alternate source for transplantation to address the ongoing shortage of grafts. Although ongoing advancements in bioengineering technology have moved the organoid transplant approach to the next level, sustained survival of the transplanted tissue still eludes us toward functional organ replacement. Herein, we review the development of HLOs and discuss promises and challenges on organoid transplant approaches.

Indexed as

Liver DiseasesPluripotent Stem CellsCell Culture TechniquesCell DifferentiationHumansLiverOrganoidsapplicationsefficacyliver organoidsafetytransplantationtransplantation sites

Identifiers

PMID34614263
PMCPMC8602742

What OpenQuestion holds

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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.