Evidence map›Paper›PMID 26673961›Full record

ArticleBBA clinical2014

Transferrin-bound proteins as potential biomarkers for advanced breast cancer patients.

Paul Dowling, Valentina Palmerini, Michael Henry, Paula Meleady, Vincent Lynch, Jo Ballot, Giuseppe Gullo, John Crown, Michael Moriarty, Martin Clynes

Open access · hybridAbstract read
In one paragraph

Article in BBA clinical, 2014. 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
1.6field-weighted citation impact, top 19% 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, 22 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 4 institutions in 2 countries.

Paul DowlingDepartment of Biology, Maynooth University, Maynooth, Co Kildare, Ireland ; National Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Valentina PalmeriniEuropean Institute of Oncology, IFOM-IEO-Campus, Department of Experimental Oncology, Milan, Italy.
Michael HenryNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Paula MeleadyNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Vincent LynchNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Jo BallotMolecular Therapeutics for Cancer Ireland (MTCI), Dublin, Ireland ; St. Vincent's University Hospital, Dublin, Ireland.
Giuseppe GulloMolecular Therapeutics for Cancer Ireland (MTCI), Dublin, Ireland ; St. Vincent's University Hospital, Dublin, Ireland.
John CrownMolecular Therapeutics for Cancer Ireland (MTCI), Dublin, Ireland ; St. Vincent's University Hospital, Dublin, Ireland.
Michael MoriartyNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Martin ClynesNational Institute for Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Dublin City University · IESt. Vincent's University Hospital · IEEuropean Institute of Oncology · ITNational University of Ireland, Maynooth · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerum profiling using mass spectrometry-based proteomic techniques has great potential to detect biomarkers that might improve the management for advanced breast cancer patients. The albuminome has previously been investigated as a tool in biomarker discovery, however other high abundant blood proteins are also likely to sequester potentially interesting molecules.

methodsAffinity resin purified and isolated Transferrin and associated bound proteins from normal control and breast cancer patient serum samples were analysed by label-free mass spectrometry during the discovery phase.

results21 significant proteins were identified with Fibrinogen and Fibronectin selected for further analysis in an independent sample set, with significant difference found when comparing the controls groups (normal healthy control, inflammatory bowel disease and benign breast disease) to stage IV breast cancer.

conclusionsThe area under the curve value for Fibrinogen compared favourably with cancer antigen 15-3, an established breast cancer tumour marker. A combination of all three biomarkers improved accuracy when comparing control/benign to stage IV breast cancer patient groups. GENERAL SIGNIFICANCE: Mass spectrometry profiling of Transferrin-bound proteins has revealed serum proteins that can distinguish between serum from advanced breast cancer patients and healthy control subjects with high confidence.

Indexed as

BiomarkersBreast cancerFibrinogenFibronectinMass spectrometryTransferrin

Identifiers

PMID26673961
PMCPMC4633920
OpenAlexW2024790065

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.