Evidence map›Paper›PMID 30963621›Full record

ArticleJournal of applied toxicology : JAT2019

A novel screening method for transition metal-based anticancer compounds using zebrafish embryo-larval assay and inductively coupled plasma-mass spectrometry analysis.

Brittany F Karas, Leonor Côrte-Real, Cathleen L Doherty, Andreia Valente, Keith R Cooper, Brian T Buckley

Open access · greenAbstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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  6. Supercritical COACS omega · 2020
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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

6 authors at 2 institutions in 2 countries.

Brittany F KarasJoint Graduate Program in Toxicology, Rutgers, The State University of New Jersey, Piscataway, NJ, 08854, USA.ORCID 0000-0002-1738-7235
Leonor Côrte-RealCentro de Química Estrutural, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749-016, Lisbon, Portugal.
Cathleen L DohertyEnvironmental and Occupational Health Sciences Institute, Rutgers University, 170 Frelinghuysen Road, Piscataway, NJ, 08854, USA.ORCID 0000-0001-8831-6330
Andreia ValenteCentro de Química Estrutural, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749-016, Lisbon, Portugal.
Keith R CooperEnvironmental and Occupational Health Sciences Institute, Rutgers University, 170 Frelinghuysen Road, Piscataway, NJ, 08854, USA.ORCID 0000-0002-5233-5270
Brian T BuckleyEnvironmental and Occupational Health Sciences Institute, Rutgers University, 170 Frelinghuysen Road, Piscataway, NJ, 08854, USA.ORCID 0000-0001-7336-4321
Rutgers, The State University of New Jersey · USUniversity of Lisbon · PT

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI PANOS G. GEORGOPOULOS · 1988 to 2026
$47.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
CEEC Individual 2017 CEECIND/01974/2017Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa IF/01302/2013Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa PTDC/QUI-QIN/28662/2017Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa SFRH/BD/100515/2014Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa UID/QUI/00100/2013FSE - European Social FundNew Jersey Agricultural Experiment Station 01202 (W2045)New Jersey Agricultural Experiment Station NJ01201NIEHS NIH HHS P30 ES005022NIEHS NIH HHS T32 ES007148NIEHS NIH HHS T32-ES 007148
6 · The paper itself

Abstract

As novel metallodrugs continue to emerge, they are evaluated using models, including zebrafish, that offer unique sublethal endpoints. Testing metal-based anticancer compounds with high-throughput zebrafish toxicological assays requires analytical methods with the sensitivity to detect these sublethal tissue doses in very small sample masses (e.g., egg mass 100 μg). A robust bioanalytical model, zebrafish embryos coupled with inductively coupled plasma-mass spectrometry (ICPMS) for measurement of delivered dose, creates a very effective means for screening metal-based chemotherapeutic agents. In this study, we used ICPMS quantitation with the zebrafish embryo assays to detect metal equivalents at multiple response endpoints for two compounds, the chemotherapeutic agent cisplatin and ruthenium (Ru)-based prospective metallodrug, PMC79. We hypothesized that cisplatin and PMC79 have different mechanisms for inducing apoptosis and result in similar lesions but different potencies following water-borne exposure. An ICPMS method was developed to detect the metal in waterborne solution and tissue (detection limit: 5 parts per trillion for Ru or platinum [Pt]). The Ru-based compound was more potent (LC

Indexed as

ZebrafishAnimalsAntineoplastic AgentsApoptosisBiological AssayCisplatinDose-Response Relationship, DrugEmbryonic DevelopmentEmbryo, NonmammalianLarvaOrganometallic CompoundsRutheniumSpectrophotometry, AtomicAntineoplastic AgentsCisplatinOrganometallic CompoundsRutheniumanalyticalanticancer agentscisplatindose-responseICPMSMetallodrugsruthenium organometallic compoundssublethalzebrafish

Identifiers

PMID30963621
PMCPMC6625851
OpenAlexW2936877252

What OpenQuestion holds

Textmetadata
LicenceTDM
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.