Evidence map›Paper›PMID 25324538›Full record

ArticleJournal of radiation research2015

Co-visualization of DNA damage and ion traversals in live mammalian cells using a fluorescent nuclear track detector.

Satoshi Kodaira, Teruaki Konishi, Alisa Kobayashi, Takeshi Maeda, Tengku Ahbrizal Farizal Tengku Ahmad, Gen Yang, Mark S Akselrod, Yoshiya Furusawa, Yukio Uchihori

Open access · goldAbstract read
In one paragraph

Article in Journal of radiation research, 2015. 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
0.4field-weighted citation impact, top 35% 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, 33 citations in OpenAlex.

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  5. Evidence of Local Concentration of α-Particles fromJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
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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

9 authors at 3 institutions in 3 countries.

Satoshi KodairaResearch, Development and Support Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inageku, Chiba 263-8555, Japan.
Teruaki KonishiResearch, Development and Support Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inageku, Chiba 263-8555, Japan tkonishi@nirs.go.jp.
Alisa KobayashiResearch, Development and Support Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inageku, Chiba 263-8555, Japan.
Takeshi MaedaResearch, Development and Support Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inageku, Chiba 263-8555, Japan.
Tengku Ahbrizal Farizal Tengku AhmadDivision of Agrotechnology and Biosciences, Malaysian Nuclear Agency, Bangi, Kajang 43000, Malaysia.
Gen YangState Key Laboratory of Nuclear Physics and Technology, Peking University, Beijing 100871, PR China.
Mark S AkselrodLandauer Inc., Crystal Growth Division, Stillwater, OK 74074, USA.
Yoshiya FurusawaResearch, Development and Support Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inageku, Chiba 263-8555, Japan.
Yukio UchihoriResearch, Development and Support Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inageku, Chiba 263-8555, Japan.
Landauer (United States) · USMalaysian Nuclear Agency · MYPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The geometric locations of ion traversals in mammalian cells constitute important information in the study of heavy ion-induced biological effect. Single ion traversal through a cellular nucleus produces complex and massive DNA damage at a nanometer level, leading to cell inactivation, mutations and transformation. We present a novel approach that uses a fluorescent nuclear track detector (FNTD) for the simultaneous detection of the geometrical images of ion traversals and DNA damage in single cells using confocal microscopy. HT1080 or HT1080-53BP1-GFP cells were cultured on the surface of a FNTD and exposed to 5.1-MeV/n neon ions. The positions of the ion traversals were obtained as fluorescent images of a FNTD. Localized DNA damage in cells was identified as fluorescent spots of γ-H2AX or 53BP1-GFP. These track images and images of damaged DNA were obtained in a short time using a confocal laser scanning microscope. The geometrical distribution of DNA damage indicated by fluorescent γ-H2AX spots in fixed cells or fluorescent 53BP1-GFP spots in living cells was found to correlate well with the distribution of the ion traversals. This method will be useful for evaluating the number of ion hits on individual cells, not only for micro-beam but also for random-beam experiments.

Indexed as

Cell Line, TumorCell SurvivalDNA DamageEquipment DesignEquipment Failure AnalysisFibrosarcomaHumansIonsLinear Energy TransferMicroscopy, ConfocalMicroscopy, FluorescenceRadiation DosageRadiometryReproducibility of ResultsSensitivity and SpecificityIonsDNA damagefluorescent nuclear track detectorion beam trackslocalization

Identifiers

PMID25324538
PMCPMC4380042
OpenAlexW2120443606

What OpenQuestion holds

Textmetadata
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.