Evidence map›Paper›PMID 30602943›Full record

ArticleClinical proteomics2018

Proteomics identification of radiation-induced changes of membrane proteins in the rat model of arteriovenous malformation in pursuit of targets for brain AVM molecular therapy.

Margaret Simonian, Dyna Shirasaki, Vivienne S Lee, David Bervini, Michael Grace, Rachel R Ogorzalek Loo, Joseph A Loo, Mark P Molloy, Marcus A Stoodley

Abstract read
In one paragraph

Article in Clinical proteomics, 2018. 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
–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

7 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

9 authors.

Margaret Simonian1Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW Australia.
Dyna Shirasaki2Department of Biological Chemistry, David Geffen School of Medicine, University of California Los Angeles (UCLA), 611 Charles E. Young Drive East, Los Angeles, CA 90095 USA.
Vivienne S Lee1Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW Australia.
David Bervini1Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW Australia.
Michael Grace4Genesis Cancer Care, Macquarie University Hospital, Sydney, NSW Australia.
Rachel R Ogorzalek Loo2Department of Biological Chemistry, David Geffen School of Medicine, University of California Los Angeles (UCLA), 611 Charles E. Young Drive East, Los Angeles, CA 90095 USA.
Joseph A Loo2Department of Biological Chemistry, David Geffen School of Medicine, University of California Los Angeles (UCLA), 611 Charles E. Young Drive East, Los Angeles, CA 90095 USA.
Mark P Molloy5Department of Chemistry and Bimolecular Sciences, Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney, NSW Australia.
Marcus A Stoodley1Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRapid identification of novel targets and advancement of a vascular targeting strategy requires a comprehensive assessment of AVM endothelial membrane protein changes in response to irradiation. The aim of this study is to provide additional potential target protein molecules for evaluation in animal trials to promote intravascular thrombosis in AVM vessels post radiosurgery.

methodsWe employed in vivo biotinylation methodology that we developed, to label membrane proteins in the rat model of AVM post radiosurgery. Mass spectrometry expression (MS

resultsOur proteomics data revealed differentially expressed membrane proteins between irradiated and non irradiated rats, e.g. profilin-1, ESM-1, ion channel proteins, annexin A2 and lumican.

conclusionThis work provides additional potential target protein molecules for evaluation in animal trials to promote intravascular thrombosis in AVM vessels post radiosurgery.

Indexed as

AVM animal modelIn vivo biotinylationMembrane proteinsRadiosurgery

Identifiers

PMID30602943
PMCPMC6305998

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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.