Evidence map›Paper›PMID 36823355›Full record

ArticleNature biotechnology2023

Engineered human hepatocyte organoids enable CRISPR-based target discovery and drug screening for steatosis.

Delilah Hendriks, Jos F Brouwers, Karien Hamer, Maarten H Geurts, Léa Luciana, Simone Massalini, Carmen López-Iglesias, Peter J Peters, Maria J Rodríguez-Colman, Susana Chuva de Sousa Lopes and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Nature biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed
45.3field-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

131 citing papers in PubMed, 211 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Precision pathophysiology in steatotic liver disease.Clinical and molecular hepatology · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. New developments and applications of human organoids.Nature reviews. Molecular cell biology · 2026
    Review
  12. Review
  13. CRISPR Gene Tagging for Illuminating Endogenous Protein Dynamics.International journal of molecular sciences · 2026
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
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  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 2 countries.

Delilah HendriksHubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands. d.hendriks@hubrecht.eu.ORCID 0000-0003-1159-5946
Jos F BrouwersResearch Group Analysis Techniques in the Life Sciences, School of Life Sciences and Technology, Avans University of Applied Sciences, Breda, The Netherlands.ORCID 0000-0003-2924-3279
Karien HamerHubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands.
Maarten H GeurtsHubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands.
Léa LucianaHubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands.ORCID 0000-0003-0741-7071
Simone MassaliniThe Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Carmen López-IglesiasThe Maastricht Multimodal Molecular Imaging Institute, Maastricht University, Maastricht, The Netherlands.
Peter J PetersThe Maastricht Multimodal Molecular Imaging Institute, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-2964-5684
Maria J Rodríguez-ColmanMolecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Susana Chuva de Sousa LopesDepartment of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-3866-2803
Benedetta Artegiani *Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands. b.a.artegiani@prinsesmaximacentrum.nl.ORCID 0000-0002-0904-4187
Hans Clevers *Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands. h.clevers@hubrecht.eu.ORCID 0000-0002-3077-5582
Royal Netherlands Academy of Arts and Sciences · NLMaastricht University · NLAvans University of Applied Sciences · NLLeiden University Medical Center · NLPrincess Máxima Center · NLRoche (Switzerland) · CHUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lack of registered drugs for nonalcoholic fatty liver disease (NAFLD) is partly due to the paucity of human-relevant models for target discovery and compound screening. Here we use human fetal hepatocyte organoids to model the first stage of NAFLD, steatosis, representing three different triggers: free fatty acid loading, interindividual genetic variability (PNPLA3 I148M) and monogenic lipid disorders (APOB and MTTP mutations). Screening of drug candidates revealed compounds effective at resolving steatosis. Mechanistic evaluation of effective drugs uncovered repression of de novo lipogenesis as the convergent molecular pathway. We present FatTracer, a CRISPR screening platform to identify steatosis modulators and putative targets using APOB

Indexed as

Non-alcoholic Fatty Liver DiseaseApolipoproteins BDrug Evaluation, PreclinicalHepatocytesHumansLipid MetabolismLiverApolipoproteins B

Identifiers

PMID36823355
PMCPMC10635827
OpenAlexW4321611246

What OpenQuestion holds

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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.