Evidence map›Paper›PMID 26137966›Full record

ArticleBMC medicine2015

Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis.

Marcelo Sobral-Leite, Jelle Wesseling, Vincent T H B M Smit, Heli Nevanlinna, Martine H van Miltenburg, Joyce Sanders, Ingrid Hofland, Fiona M Blows, Penny Coulson, Gazinska Patrycja and 37 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The role and application prospects of ANXA1 in gastric cancer cells.Medical oncology (Northwood, London, England) · 2025
    Review
  4. Review
  5. The Immune Response of Cancer Cells in Breast and Gynecologic Neoplasms.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Review
  8. Article
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  10. Review
  11. Article
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  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Frontiers in oncology · 2020
    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

47 authors at 20 institutions in 8 countries.

Marcelo Sobral-LeiteDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. m.leite@nki.nl.
Jelle WesselingDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. j.wesseling@nki.nl.
Vincent T H B M SmitDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands. V.T.H.B.M.Smit@lumc.nl.
Heli NevanlinnaUniversity of Helsinki, Helsinki, Finland. Heli.Nevanlinna@hus.fi.
Martine H van MiltenburgDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. m.v.miltenburg@nki.nl.
Joyce SandersDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. jo.sanders@nki.nl.
Ingrid HoflandCore Facility Molecular Pathology and Biobanking, Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. i.hofland@nki.nl.
Fiona M BlowsCentre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK. fmb28@medschl.cam.ac.uk.
Penny CoulsonDivision of Genetics and Epidemiology, Institute of Cancer Research, London, UK. Penny.Coulson@icr.ac.uk.
Gazinska PatrycjaBreakthrough Breast Cancer Centre, London, UK. patrycja.gazinska@kcl.ac.uk.
Jan H M SchellensDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. j.schellens@nki.nl.
Rainer FagerholmUniversity of Helsinki, Helsinki, Finland. rainer.fagerholm@helsinki.fi.
Päivi HeikkiläUniversity of Helsinki, Helsinki, Finland. paivi.heikkila@hus.fi.
Kristiina AittomäkiUniversity of Helsinki, Helsinki, Finland. kristiina.aittomaki@helsinki.fi.
Carl BlomqvistUniversity of Helsinki, Helsinki, Finland. carl.blomqvist@helsinki.fi.
Elena ProvenzanoCancer Research UK Cambridge Institute Oncology, University of Cambridge, Cambridge, UK. elena.provenzano@addenbrookes.nhs.uk.
Hamid Raza AliCancer Research UK Cambridge Institute Oncology, University of Cambridge, Cambridge, UK. Raza.Ali@cruk.cam.ac.uk.
Jonine FigueroaDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA. figueroaj@mail.nih.gov.
Mark ShermanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA. shermanm@exchange.nih.gov.
Jolanta LissowskaDepartment of Cancer Epidemiology and Prevention, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland. lissowsj@coi.waw.pl.
Arto MannermaaSchool of Medicine, Institute of Clinical Medicine, Pathology and Forensic Medicine, University of Eastern Finland, Kuopio, Finland. arto.mannermaa@uef.fi.
Vesa KatajaCancer Center, Kuopio University Hospital, Kuopio, Finland. vesa.kataja@ksshp.fi.
Veli-Matti KosmaSchool of Medicine, Institute of Clinical Medicine, Pathology and Forensic Medicine, University of Eastern Finland, Kuopio, Finland. veli-matti.kosma@uef.fi.
Jaana M HartikainenSchool of Medicine, Institute of Clinical Medicine, Pathology and Forensic Medicine, University of Eastern Finland, Kuopio, Finland. jaana.hartikainen@uef.fi.
Kelly-Anne PhillipsDivision of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, Australia. Kelly.Phillips@petermac.org.
kConFab/AOCS Investigators
Fergus J CouchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA. couch.fergus@mayo.edu.
Janet E OlsonDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA. olsonj@mayo.edu.
Celine VachonDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA. vachon.celine@mayo.edu.
Daniel VisscherDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA. visscher.daniel@mayo.edu.
Hermann BrennerDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany. h.brenner@dkfz.de.
Katja ButterbachDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany. k.butterbach@dkfz.de.
Volker ArndtDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany. v.arndt@dkfz.de.
Bernd HolleczekSaarland Cancer Registry, Saarbrücken, Germany. B.Holleczek@gbe-ekr.saarland.de.
Maartje J HooningDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. m.hooning@erasmusmc.nl.
Antoinette HollestelleDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. a.hollestelle@erasmusmc.nl.
John W M MartensDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. j.martens@erasmusmc.nl.
Carolien H M van DeurzenDepartment of Pathology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. c.h.m.vandeurzen@erasmusmc.nl.
Bob van de WaterDivision of Toxicology, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands. b.water@lacdr.leidenuniv.nl.
Annegien BroeksCore Facility Molecular Pathology and Biobanking, Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. a.broeks@nki.nl.
Jenny Chang-ClaudeDivision of Cancer Epidemiology, Unit of Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany. j.chang-claude@dkfz-heidelberg.de.
Georgia Chenevix-TrenchDepartment of Genetics, QIMR Berghofer Medical Research Institute, Brisbane, Australia. Georgia.Trench@qimrberghofer.edu.au.
Douglas F EastonCentre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK. dfe20@medschl.cam.ac.uk.
Paul D P PharoahCentre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK. paul.pharoah@srl.cam.ac.uk.
Montserrat García-ClosasDivision of Genetics and Epidemiology, Institute of Cancer Research, London, UK. Montse.GarciaClosas@icr.ac.uk.
Marjo de GraauwDivision of Toxicology, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands. m.de.graauw@lacdr.leidenuniv.nl.
Marjanka K SchmidtDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. mk.schmidt@nki.nl.
Oncode Institute · NLGerman Cancer Research Center · DEUniversity of Helsinki · FIErasmus MC Cancer Institute · NLLeiden University · NLUniversity of Eastern Finland · FIMayo Clinic · USMayo Clinic in Arizona · USNational Cancer Institute · USBreast Cancer Care · GBBreast Cancer Now · GBCambridge University Hospitals NHS Foundation Trust · GBCancer Research UK · GBCancer Research UK Cambridge Center · GBInstitute of Cancer Research · GBKuopio University Hospital · FILeiden University Medical Center · NLQIMR Berghofer Medical Research Institute · AUThe Maria Sklodowska-Curie National Research Institute of Oncology · PLThe University of Melbourne · AU

Funding

Hormone-Related CancersZIACP010126 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI GIERACH, GRETCHEN · 2009 to 2025
$103.5M
The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
A genome-wide association study for breast cancer in BRCA1 mutation carriersR01CA128978 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2008 to 2012
$4.8M
Identifying and validating novel susceptibility genes for breast cancerR01CA176785 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, NATHANSON, KATHERINE L. · 2014 to 2018
$3.4M
BRCA2 missense mutations and breast cancerR01CA116167 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2007 to 2011
$3.0M
BRCA1 and BRCA2 missense mutations and breast cancer riskU01CA116167 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2013 to 2017
$2.7M
Cancer Research UK 10124Cancer Research UK 16561Cancer Research UK 16563Cancer Research UK C1287/A10118Cancer Research UK C1287/A12014Cancer Research UK C490/A10119Cancer Research UK C490/A10124Cancer Research UK C490/A16561NCI NIH HHS CA116167NCI NIH HHS CA116201NCI NIH HHS CA128978NCI NIH HHS CA176785NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA116167NCI NIH HHS R01 CA128978NCI NIH HHS R01 CA176785NCI NIH HHS U01 CA116167
6 · The paper itself

Abstract

backgroundAnnexin A1 (ANXA1) is a protein related with the carcinogenesis process and metastasis formation in many tumors. However, little is known about the prognostic value of ANXA1 in breast cancer. The purpose of this study is to evaluate the association between ANXA1 expression, BRCA1/2 germline carriership, specific tumor subtypes and survival in breast cancer patients.

methodsClinical-pathological information and follow-up data were collected from nine breast cancer studies from the Breast Cancer Association Consortium (BCAC) (n = 5,752) and from one study of familial breast cancer patients with BRCA1/2 mutations (n = 107). ANXA1 expression was scored based on the percentage of immunohistochemical staining in tumor cells. Survival analyses were performed using a multivariable Cox model.

resultsThe frequency of ANXA1 positive tumors was higher in familial breast cancer patients with BRCA1/2 mutations than in BCAC patients, with 48.6 % versus 12.4 %, respectively; P <0.0001. ANXA1 was also highly expressed in BCAC tumors that were poorly differentiated, triple negative, EGFR-CK5/6 positive or had developed in patients at a young age. In the first 5 years of follow-up, patients with ANXA1 positive tumors had a worse breast cancer-specific survival (BCSS) than ANXA1 negative (HRadj = 1.35; 95 % CI = 1.05-1.73), but the association weakened after 10 years (HRadj = 1.13; 95 % CI = 0.91-1.40). ANXA1 was a significant independent predictor of survival in HER2+ patients (10-years BCSS: HRadj = 1.70; 95 % CI = 1.17-2.45).

conclusionsANXA1 is overexpressed in familial breast cancer patients with BRCA1/2 mutations and correlated with poor prognosis features: triple negative and poorly differentiated tumors. ANXA1 might be a biomarker candidate for breast cancer survival prediction in high risk groups such as HER2+ cases.

Indexed as

AdultAnnexin A1Biomarkers, TumorBreast NeoplasmsFemaleGenes, BRCA1Genes, BRCA2Genetic Predisposition to DiseaseHumansImmunohistochemistryMiddle AgedMutationPrognosisAnnexin A1Biomarkers, Tumor

Identifiers

PMID26137966
PMCPMC4489114
OpenAlexW1497435151

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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.