Evidence map›Paper›PMID 23146835›Full record

ArticleMolecular & cellular proteomics : MCP2013

Alteration of the serum N-glycome of mice locally exposed to high doses of ionizing radiation.

Thibault Chaze, Marie-Christine Slomianny, Fabien Milliat, Georges Tarlet, Tony Lefebvre-Darroman, Patrick Gourmelon, Eric Bey, Marc Benderitter, Jean-Claude Michalski, Olivier Guipaud

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Thibault ChazeInstitut de Radioprotection et de Sûreté Nucléaire (IRSN), DRPH, SRBE, LRTE, 92260 Fontenay-aux-Roses, France.
Marie-Christine Slomianny
Fabien Milliat
Georges Tarlet
Tony Lefebvre-Darroman
Patrick Gourmelon
Eric Bey
Marc Benderitter
Jean-Claude Michalski
Olivier Guipaud
Institut de Radioprotection et de Sûreté Nucléaire · FRUnité de Glycobiologie Structurale et Fonctionnelle · FRHôpital d'instruction des Armées Percy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exposure of the skin to ionizing radiation leads to characteristic reactions that will often turn into a pathophysiological process called the cutaneous radiation syndrome. The study of this disorder is crucial to finding diagnostic and prognostic bioindicators of local radiation exposure or radiation effects. It is known that irradiation alters the serum proteome content and potentially post-translationally modifies serum proteins. In this study, we investigated whether localized irradiation of the skin alters the serum glycome. Two-dimensional differential in-gel electrophoresis of serum proteins from a man and from mice exposed to ionizing radiation showed that potential post-translational modification changes occurred following irradiation. Using a large-scale quantitative mass-spectrometry-based glycomic approach, we performed a global analysis of glycan structures of serum proteins from non-irradiated and locally irradiated mice exposed to high doses of γ-rays (20, 40, and 80 Gy). Non-supervised descriptive statistical analyses (principal component analysis) using quantitative glycan structure data allowed us to discriminate between uninjured/slightly injured animals and animals that developed severe lesions. Decisional statistics showed that several glycan families were down-regulated whereas others increased, and that particular structures were statistically significantly changed in the serum of locally irradiated mice. The observed increases in multiantennary N-glycans and in outer branch fucosylation and sialylation were associated with the up-regulation of genes involved in glycosylation in the liver, which is the main producer of serum proteins, and with an increase in the key proinflammatory serum cytokines IL-1β, IL-6, and TNFα, which can regulate the expression of glycosylation genes. Our results suggest for the first time a role of serum protein glycosylation in response to irradiation. These protein-associated glycan structure changes might signal radiation exposure or effects.

Indexed as

Protein Processing, Post-TranslationalAdultAnimalsBlood ProteinsBurnsCarbohydrate SequenceElectrophoresis, Gel, Two-DimensionalGamma RaysGene Expression RegulationGlycomicsGlycosylationHumansInterleukin-1betaInterleukin-6LiverMaleBlood ProteinsInterleukin-1betaInterleukin-6PolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID23146835
PMCPMC3567854
OpenAlexW2116861031

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.