Evidence map›Paper›PMID 27859262›Full record

ArticleThe Journal of pathology2017

Functional and prognostic significance of the genomic amplification of frizzled 6 (FZD6) in breast cancer.

Gabriele Corda, Gianluca Sala, Rossano Lattanzio, Manuela Iezzi, Michele Sallese, Giorgia Fragassi, Alessia Lamolinara, Hasan Mirza, Daniela Barcaroli, Sibylle Ermler and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.5field-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

47 citing papers in PubMed, 72 citations in OpenAlex.

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  15. A Signature of NFrontiers in immunology · 2022
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  20. Wnt/β-catenin signaling in cancers and targeted therapies.Signal transduction and targeted therapy · 2021
    Review
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

25 authors at 7 institutions in 4 countries.

Gabriele CordaCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Gianluca SalaMediaPharma srl, Chieti, Italy.
Rossano LattanzioDipartimento di Scienze Mediche, Orali e Biotecnologiche, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Manuela IezziDipartimento di Medicina e Scienze dell'Invecchiamento, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Michele SalleseDipartimento di Scienze Mediche, Orali e Biotecnologiche, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Giorgia FragassiDipartimento di Scienze Mediche, Orali e Biotecnologiche, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Alessia LamolinaraDipartimento di Medicina e Scienze dell'Invecchiamento, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Hasan MirzaBreast Cancer Now Unit, Research Oncology, King's Health Partners AHSC, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Daniela BarcaroliDipartimento di Scienze Psicologiche, della Salute e del Territorio, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Sibylle ErmlerCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Elisabete SilvaCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Hemad YasaeiCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Robert F NewboldCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Paola VagnarelliCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Marcella MottoleseRegina Elena Cancer Institute, Rome, Italy.
Pier Giorgio NataliMediaPharma srl, Chieti, Italy.
Letizia PerracchioRegina Elena Cancer Institute, Rome, Italy.
Jelmar QuistBreast Cancer Now Unit, Research Oncology, King's Health Partners AHSC, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Anita GrigoriadisBreast Cancer Now Unit, Research Oncology, King's Health Partners AHSC, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Pierfrancesco MarraBreast Cancer Now Unit, Research Oncology, King's Health Partners AHSC, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Andrew N TuttBreast Cancer Now Unit, Research Oncology, King's Health Partners AHSC, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Mauro PiantelliDipartimento di Scienze Mediche, Orali e Biotecnologiche, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Stefano IacobelliMediaPharma srl, Chieti, Italy.
Vincenzo De LaurenziDipartimento di Scienze Mediche, Orali e Biotecnologiche, CESI-MeT, University G. D'Annunzio, Chieti, Italy.
Arturo SalaCollege of Health and Life Sciences, Brunel University London, Uxbridge, UK.
University of Chieti-Pescara · ITBrunel University of London · GBKing's College London · GBBreast Cancer Now · GBNational Cancer Institute · MYCTI BioPharma (Italy) · ITMario Negri Sud Foundation · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Frizzled receptors mediate Wnt ligand signalling, which is crucially involved in regulating tissue development and differentiation, and is often deregulated in cancer. In this study, we found that the gene encoding the Wnt receptor frizzled 6 (FZD6) is frequently amplified in breast cancer, with an increased incidence in the triple-negative breast cancer (TNBC) subtype. Ablation of FZD6 expression in mammary cancer cell lines: (1) inhibited motility and invasion; (2) induced a more symmetrical shape of organoid three-dimensional cultures; and (3) inhibited bone and liver metastasis in vivo. Mechanistically, FZD6 signalling is required for the assembly of the fibronectin matrix, interfering with the organization of the actin cytoskeleton. Ectopic delivery of fibronectin in FZD6-depleted, triple-negative MDA-MB-231 cells rearranged the actin cytoskeleton and restored epidermal growth factor-mediated invasion. In patients with localized, lymph node-negative (early) breast cancer, positivity of tumour cells for FZD6 protein identified patients with reduced distant relapse-free survival. Multivariate analysis indicated an independent prognostic significance of FZD6 expression in TNBC tumours, predicting distant, but not local, relapse. We conclude that the FZD6-fibronectin actin axis identified in our study could be exploited for drug development in highly metastatic forms of breast cancer, such as TNBC. © 2016 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

Breast NeoplasmsCell Line, TumorCell MovementFemaleFrizzled ReceptorsGenomicsHumansNeoplasm Recurrence, LocalPrognosisSignal TransductionFrizzled ReceptorsFZD6 protein, humanactin cytoskeletonmetastasismouse modelWnt signallingxenograft

Identifiers

PMID27859262
PMCPMC5248601
OpenAlexW2553012279

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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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.