Evidence map›Paper›PMID 34359605›Full record

ArticleCancers2021

Systematic Roadmap for Cancer Drug Screening Using Zebrafish Embryo Xenograft Cancer Models: Melanoma Cell Line as a Case Study.

Patricia Letrado, Holly Mole, María Montoya, Irene Palacios, Jorge Barriuso, Adam Hurlstone, Roberto Díez-Martínez, Julen Oyarzabal

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

8 authors.

Patricia LetradoIkan Biotech SL, Centro Europeo de Empresas e Innovación de Navarra (CEIN), 31110 Noain, Spain.
Holly MoleDivision of Cancer Sciences, School of Medical Sciences, The University of Manchester, Manchester M13 9PL, UK.
María MontoyaCellomics Unit, Spanish National Center for Cardiovascular Research (CNIC), 28029 Madrid, Spain.
Irene PalaciosCellomics Unit, Spanish National Center for Cardiovascular Research (CNIC), 28029 Madrid, Spain.
Jorge BarriusoDivision of Cancer Sciences, School of Medical Sciences, The University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0002-5641-9105
Adam HurlstoneDivision of Infection, Immunology and Respiratory Medicine, School of Biological Science, The University of Manchester, Manchester M13 9PT, UK.ORCID 0000-0001-5260-9457
Roberto Díez-MartínezIkan Biotech SL, Centro Europeo de Empresas e Innovación de Navarra (CEIN), 31110 Noain, Spain.
Julen OyarzabalCenter for Applied Medical Research (CIMA), University of Navarra, 31008 Pamplona, Spain.

Funding

Gobierno de Navarra 0011-1365-2020-000292Gobierno de Navarra 0011-1408-2016-000004
6 · The paper itself

Abstract

Zebrafish embryo tumor transplant models are widely utilized in cancer research. Compared with traditional murine models, the small size and transparency of zebrafish embryos combined with large clutch sizes that increase statistical power and cheap husbandry make them a cost-effective and versatile tool for in vivo drug discovery. However, the lack of a comprehensive analysis of key factors impacting the successful use of these models impedes the establishment of basic guidelines for systematic screening campaigns. Thus, we explored the following crucial factors: (i) user-independent inclusion criteria, focusing on sample homogeneity; (ii) metric definition for data analysis; (iii) tumor engraftment criteria; (iv) image analysis versus quantification of human cancer cells using qPCR (RNA and gDNA); (v) tumor implantation sites; (vi) compound distribution (intratumoral administration versus alternative inoculation sites); and (vii) efficacy (intratumoral microinjection versus compound solution in media). Based on these analyses and corresponding assessments, we propose the first roadmap for systematic drug discovery screening in zebrafish xenograft cancer models using a melanoma cell line as a case study. This study aims to help the wider cancer research community to consider the adoption of this versatile model for cancer drug screening projects.

Indexed as

cancerdrug discoveryroadmapscreeningxenograftzebrafish

Identifiers

PMID34359605
PMCPMC8345186

What OpenQuestion holds

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LicenceCC BY
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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.