Evidence map›Paper›PMID 32665567›Full record

ArticleScientific reports2020

MALDI-MSI spatially maps N-glycan alterations to histologically distinct pulmonary pathologies following irradiation.

Claire L Carter, George A Parker, Kim G Hankey, Ann M Farese, Thomas J MacVittie, Maureen A Kane

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. IntegratingMolecular omics · 2025
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  8. Review
  9. Review
  10. Article
  11. High sensitivity glycomics in biomedicine.Mass spectrometry reviews · 2022
    Review
  12. Spatial Mapping of PlantFrontiers in plant science · 2022
    Article
  13. Review
  14. Review
  15. Article
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 1 country.

Claire L CarterDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD, USA.
George A ParkerPathology Associates, Charles River Laboratories, Raleigh-Durham, NC, USA.
Kim G HankeyDepartment of Radiation Oncology, School of Medicine, University of Maryland, Maryland, USA.ORCID http://orcid.org/0000-0003-1699-6087
Ann M FareseDepartment of Radiation Oncology, School of Medicine, University of Maryland, Maryland, USA.
Thomas J MacVittieDepartment of Radiation Oncology, School of Medicine, University of Maryland, Maryland, USA.
Maureen A KaneDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD, USA. mkane@rx.umaryland.edu.ORCID http://orcid.org/0000-0002-5525-9170
University of Maryland, Baltimore · USCharles River Laboratories (United States) · US

Funding

NIAID NIH HHS HHSN272201000046CNIAID NIH HHS HHSN272201500013I
6 · The paper itself

Abstract

Radiation-induced lung injury is a highly complex combination of pathological alterations that develop over time and severity of disease development is dose-dependent. Following exposures to lethal doses of irradiation, morbidity and mortality can occur due to a combination of edema, pneumonitis and fibrosis. Protein glycosylation has essential roles in a plethora of biological and immunological processes. Alterations in glycosylation profiles have been detected in diseases ranging from infection, inflammation and cancer. We utilized mass spectrometry imaging to spatially map N-glycans to distinct pathological alterations during the clinically latent period and at 180 days post-exposure to irradiation. Results identified alterations in a number of high mannose, hybrid and complex N-glycans that were localized to regions of mucus and alveolar-bronchiolar hyperplasia, proliferations of type 2 epithelial cells, accumulations of macrophages, edema and fibrosis. The glycosylation profiles indicate most alterations occur prior to the onset of clinical symptoms as a result of pathological manifestations. Alterations in five N-glycans were identified as a function of time post-exposure. Understanding the functional roles N-glycans play in the development of these pathologies, particularly in the accumulation of macrophages and their phenotype, may lead to new therapeutic avenues for the treatment of radiation-induced lung injury.

Indexed as

AnimalsEdemaGlycosylationInflammationLungLung InjuryMacaca mulattaMacrophagesMacrophages, AlveolarMaleMannosePhenotypePneumoniaPolysaccharidesPulmonary FibrosisRadiation InjuriesMannosePolysaccharides

Identifiers

PMID32665567
PMCPMC7360629
OpenAlexW3043471831

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.