Evidence map›Paper›PMID 37202469›Full record

ReviewNPJ precision oncology2023

Refined high-content imaging-based phenotypic drug screening in zebrafish xenografts.

C Sturtzel, S Grissenberger, P Bozatzi, E Scheuringer, A Wenninger-Weinzierl, Z Zajec, J Dernovšek, S Pascoal, V Gehl, A Kutsch and 16 more

Abstract readReview
In one paragraph

Review in NPJ precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
–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, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. High-Content Screening Framework for Academic Early Drug Discovery.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  10. Article
  11. Review
  12. Zebrafish as a Model for Translational Immuno-Oncology.Journal of personalized medicine · 2025
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Small Fish, Big Answers: Zebrafish and the Molecular Drivers of Metastasis.International journal of molecular sciences · 2025
    Review
  18. Article
  19. Article
  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

26 authors.

C Sturtzel *St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
S Grissenberger *St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0002-0695-6738
P BozatziSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
E ScheuringerSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
A Wenninger-WeinzierlSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Z ZajecFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
J DernovšekFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
S PascoalSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0002-2294-8084
V GehlSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0003-0115-9016
A KutschChristian Doppler Laboratory for Advanced Polymers for Biomaterials and 3D Printing, TU Wien, Vienna, Austria.
A GranigChristian Doppler Laboratory for Advanced Polymers for Biomaterials and 3D Printing, TU Wien, Vienna, Austria.
F RifatbegovicSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0002-9956-2382
M CarreService d'Hématologie & Oncologie Pédiatrique, Timone Hospital, AP-HM, Marseille, France.ORCID http://orcid.org/0000-0003-0427-7317
A LangDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
I ValtingojerDepartment of Molecular Oncology, Sanofi Research Center, Vitry-sur-Seine, France.
J MollDepartment of Molecular Oncology, Sanofi Research Center, Vitry-sur-Seine, France.
D LötschDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
F ErhartDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
G WidhalmDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0001-6014-0273
D SurdezBalgrist University Hospital, Faculty of Medicine, University of Zurich (UZH), Zurich, Switzerland.
O DelattreINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, SIREDO Oncology Center, Institut Curie Research Center, Paris, France.
N AndréService d'Hématologie & Oncologie Pédiatrique, Timone Hospital, AP-HM, Marseille, France.
J StampflChristian Doppler Laboratory for Advanced Polymers for Biomaterials and 3D Printing, TU Wien, Vienna, Austria.
T TomašičFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.ORCID http://orcid.org/0000-0001-5534-209X
S Taschner-MandlSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. sabine.taschner@ccri.at.ORCID http://orcid.org/0000-0002-1439-5301
M DistelSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. martin.distel@ccri.at.ORCID http://orcid.org/0000-0001-5942-0817

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 116064-ITCC P4Javna Agencija za Raziskovalno Dejavnost RS (Slovenian Research Agency) J1-1717OeAD-GmbH (OEAD) SI 29/2023Österreichische Forschungsförderungsgesellschaft (Austrian Research Promotion Agency) 7940628 533Österreichischen Akademie der Wissenschaften (Austrian Academy of Sciences) DOC fellowshipVienna Science and Technology Fund (Wiener Wissenschafts-, Forschungs- und Technologiefonds) LS18-111
6 · The paper itself

Abstract

Zebrafish xenotransplantation models are increasingly applied for phenotypic drug screening to identify small compounds for precision oncology. Larval zebrafish xenografts offer the opportunity to perform drug screens at high-throughput in a complex in vivo environment. However, the full potential of the larval zebrafish xenograft model has not yet been realized and several steps of the drug screening workflow still await automation to increase throughput. Here, we present a robust workflow for drug screening in zebrafish xenografts using high-content imaging. We established embedding methods for high-content imaging of xenografts in 96-well format over consecutive days. In addition, we provide strategies for automated imaging and analysis of zebrafish xenografts including automated tumor cell detection and tumor size analysis over time. We also compared commonly used injection sites and cell labeling dyes and show specific site requirements for tumor cells from different entities. We demonstrate that our setup allows us to investigate proliferation and response to small compounds in several zebrafish xenografts ranging from pediatric sarcomas and neuroblastoma to glioblastoma and leukemia. This fast and cost-efficient assay enables the quantification of anti-tumor efficacy of small compounds in large cohorts of a vertebrate model system in vivo. Our assay may aid in prioritizing compounds or compound combinations for further preclinical and clinical investigations.

Identifiers

PMID37202469
PMCPMC10195872

What Socratic 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 Socratic graph.