Evidence map›Paper›PMID 27640676›Full record

ArticleScientific reports2016

Synchrotron microbeam irradiation induces neutrophil infiltration, thrombocyte attachment and selective vascular damage in vivo.

Daniel Brönnimann, Audrey Bouchet, Christoph Schneider, Marine Potez, Raphaël Serduc, Elke Bräuer-Krisch, Werner Graber, Stephan von Gunten, Jean Albert Laissue, Valentin Djonov

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

10 authors.

Daniel BrönnimannInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012 Bern, Switzerland.
Audrey BouchetInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012 Bern, Switzerland.
Christoph SchneiderInstitute of Pharmacology, University of Bern, Inselspital INO-F, 3010 Bern, Switzerland.
Marine PotezInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012 Bern, Switzerland.
Raphaël SerducUniversité Grenoble Alpes, EA-Rayonnement Synchrotron et Recherche Medicale, ESRF, ID17 F-38043 Grenoble, France.
Elke Bräuer-KrischBiomedical Beamline, European Synchrotron Radiation Facility, BP220, F38043 Grenoble, France.
Werner GraberInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012 Bern, Switzerland.
Stephan von GuntenInstitute of Pharmacology, University of Bern, Inselspital INO-F, 3010 Bern, Switzerland.
Jean Albert LaissueInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012 Bern, Switzerland.
Valentin DjonovInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012 Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our goal was the visualizing the vascular damage and acute inflammatory response to micro- and minibeam irradiation in vivo. Microbeam (MRT) and minibeam radiation therapies (MBRT) are tumor treatment approaches of potential clinical relevance, both consisting of parallel X-ray beams and allowing the delivery of thousands of Grays within tumors. We compared the effects of microbeams (25-100 μm wide) and minibeams (200-800 μm wide) on vasculature, inflammation and surrounding tissue changes during zebrafish caudal fin regeneration in vivo. Microbeam irradiation triggered an acute inflammatory response restricted to the regenerating tissue. Six hours post irradiation (6 hpi), it was infiltrated by neutrophils and fli1a(+) thrombocytes adhered to the cell wall locally in the beam path. The mature tissue was not affected by microbeam irradiation. In contrast, minibeam irradiation efficiently damaged the immature tissue at 6 hpi and damaged both the mature and immature tissue at 48 hpi. We demonstrate that vascular damage, inflammatory processes and cellular toxicity depend on the beam width and the stage of tissue maturation. Minibeam irradiation did not differentiate between mature and immature tissue. In contrast, all irradiation-induced effects of the microbeams were restricted to the rapidly growing immature tissue, indicating that microbeam irradiation could be a promising tumor treatment tool.

Indexed as

SynchrotronsAnimal FinsAnimalsBlood PlateletsBlood VesselsConnective TissueHemostasisInflammationNeutrophil InfiltrationPerfusionPlatelet AdhesivenessZebrafish

Identifiers

PMID27640676
PMCPMC5027521

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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.