Evidence map›Paper›PMID 26093083›Full record

ArticleOncotarget2015

Annexin A3 is a mammary marker and a potential neoplastic breast cell therapeutic target.

Bashar Zeidan, Thomas R Jackson, Samantha E T Larkin, Ramsey I Cutress, Gary R Coulton, Margaret Ashton-Key, Nick Murray, Graham Packham, Vassilis Gorgoulis, Spiros D Garbis and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Role of annexin A3 in breast cancer (Review).Molecular and clinical oncology · 2022
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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

11 authors at 4 institutions in 2 countries.

Bashar ZeidanCancer Sciences Unit, University of Southampton, Southampton, UK.
Thomas R JacksonFaculty Institute for Cancer Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
Samantha E T LarkinCancer Sciences Unit, University of Southampton, Southampton, UK.
Ramsey I CutressCancer Sciences Unit, University of Southampton, Southampton, UK.
Gary R CoultonSt. George's Medical Biomics Centre, St. George's University of London, London, UK.
Margaret Ashton-KeyCancer Sciences Unit, University of Southampton, Southampton, UK.
Nick MurrayCancer Sciences Unit, University of Southampton, Southampton, UK.
Graham PackhamCancer Sciences Unit, University of Southampton, Southampton, UK.
Vassilis GorgoulisFaculty Institute for Cancer Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
Spiros D GarbisCancer Sciences Unit, University of Southampton, Southampton, UK.
Paul A TownsendCancer Sciences Unit, University of Southampton, Southampton, UK.
University of Southampton · GBUniversity of Manchester · GBManchester Academic Health Science Centre · GBSt George's, University of London · GB

Funding

Cancer Research UK
6 · The paper itself

Abstract

Breast cancers are the most common cancer-affecting women; critically the identification of novel biomarkers for improving early detection, stratification and differentiation from benign tumours is important for the reduction of morbidity and mortality.To identify and functionally characterise potential biomarkers, we used mass spectrometry (MS) to analyse serum samples representing control, benign breast disease (BBD) and invasive breast cancer (IDC) patients. Complementary and multidimensional proteomic approaches were used to identify and validate novel serum markers.Annexin A3 (ANX A3) was found to be differentially expressed amongst different breast pathologies. The diagnostic value of serum ANX A3 was subsequently validated by ELISA in an independent serum set representing the three groups. Here, ANX A3 was significantly upregulated in the benign disease group sera compared with other groups (P < 0.0005).In addition, paired breast tissue immunostaining confirmed that ANX A3 was abundantly expressed in benign and to a lesser extent malignant neoplastic epithelium. Finally, we illustrated ANX A3 expression in cell culture lysates and conditioned media from neoplastic breast cell lines, and its role in neoplastic breast cell migration in vitro.This study confirms the novel role of ANX A3 as a mammary biomarker, regulator and therapeutic target.

Indexed as

Gene Expression Regulation, NeoplasticAgedAnnexin A3Biomarkers, TumorBreastBreast NeoplasmsCell Line, TumorCell MovementCulture Media, ConditionedEnzyme-Linked Immunosorbent AssayEpitheliumFemaleGene SilencingHumansImmunohistochemistryMass SpectrometryAnnexin A3Biomarkers, TumorCulture Media, ConditionedAnnexin A3biomarkerbreast cancermigrationneoplasm

Identifiers

PMID26093083
PMCPMC4673275
OpenAlexW2154823301

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.