Evidence map›Paper›PMID 39147444›Full record

ArticleMutation research. Genetic toxicology and environmental mutagenesis

Multiparameter imaging flow cytometry-based cytokinesis-block micronucleus assay: Reduction of culture time and blood volume for improved efficiency.

Lindsay A Beaton-Green, Jessica M Mayenburg, Leonora Marro, Sarita Cuadros Sanchez, Sylvie Lachapelle, Ruth C Wilkins

Abstract read
In one paragraph

Article in Mutation research. Genetic toxicology and environmental mutagenesis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lindsay A Beaton-GreenEnvironmental and Radiation Health Sciences Directorate, Health Canada, 775 Brookfield Road, PL 6303B, Ottawa, ON K1A 1C1, Canada.
Jessica M MayenburgEnvironmental and Radiation Health Sciences Directorate, Health Canada, 775 Brookfield Road, PL 6303B, Ottawa, ON K1A 1C1, Canada.
Leonora MarroEnvironmental and Radiation Health Sciences Directorate, Health Canada, 775 Brookfield Road, PL 6303B, Ottawa, ON K1A 1C1, Canada.
Sarita Cuadros SanchezEnvironmental and Radiation Health Sciences Directorate, Health Canada, 775 Brookfield Road, PL 6303B, Ottawa, ON K1A 1C1, Canada; University of Ottawa, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON K1H 8L6, Canada.
Sylvie LachapelleEnvironmental and Radiation Health Sciences Directorate, Health Canada, 775 Brookfield Road, PL 6303B, Ottawa, ON K1A 1C1, Canada.
Ruth C WilkinsEnvironmental and Radiation Health Sciences Directorate, Health Canada, 775 Brookfield Road, PL 6303B, Ottawa, ON K1A 1C1, Canada. Electronic address: ruth.wilkins@hc-sc.gc.ca.

Funding

Sample Engineering CoreU19AI067773 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FORNACE, ALBERT J · 2005 to 2024
$105.4M
NIAID NIH HHS U19 AI067773
6 · The paper itself

Abstract

In the event of a large-scale incident involving radiological or nuclear exposures, there is a potential for large numbers of individuals to have received doses of radiation sufficient to cause adverse health effects. It is imperative to quickly identify these individuals in order to provide information to the medical community to assist in making decisions about their treatment. The cytokinesis-block micronucleus assay is a well-established method for performing biodosimetry. This assay has previously been adapted to imaging flow cytometry and has been validated as a high-throughput option for providing dose estimates in the range of 0-10 Gy. The goal of this study was to test the ability to further optimize the assay by reducing the time of culture to 48 h from 68 h as well as reducing the volume of blood required for the analysis to 200 μL from 2 mL. These modifications would provide efficiencies in time and ease of processing impacting the ability to manage large numbers of samples and provide dose estimates in a timely manner. Results demonstrated that either the blood volume or the culture time could be reduced while maintaining dose estimates with sufficient accuracy for triage analysis. Reducing both the blood volume and culture time, however, resulted in poor dose estimates. In conclusion, depending on the needs of the scenario, either culture time or the blood volume could be reduced to improve the efficiency of analysis for mass casualty scenarios.

Indexed as

CytokinesisFlow CytometryMicronucleus TestsAnimalsBlood VolumeDose-Response Relationship, RadiationHumansTime FactorsBiodosimetryCulture conditionsCytokinesis-block micronucleus assayImaging flow cytometryMulti-parametric analysisRadiation

Identifiers

PMID39147444
PMCPMC11370997

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Registered trials

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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.