Evidence map›Paper›PMID 29382358›Full record

ArticleBreast cancer research : BCR2018

Integrin-uPAR signaling leads to FRA-1 phosphorylation and enhanced breast cancer invasion.

Matthew G Annis, Veronique Ouellet, Jonathan P Rennhack, Sylvain L'Esperance, Claudine Rancourt, Anne-Marie Mes-Masson, Eran R Andrechek, Peter M Siegel

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  4. FRA1 (Frontiers in cell and developmental biology · 2025
    Article
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  8. FRA-1 as a Regulator of EMT and Metastasis in Breast Cancer.International journal of molecular sciences · 2023
    Review
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  15. Mucinous carcinoma with micropapillary features is morphologically, clinically and genetically distinct from pure mucinous carcinoma of breast.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
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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

8 authors at 5 institutions in 2 countries.

Matthew G AnnisGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada.
Veronique OuelletCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM) and Institut du cancer de Montréal, Montreal, Canada.
Jonathan P RennhackDepartment of Physiology, Michigan State University, East Lansing, Michigan, USA.
Sylvain L'EsperanceDépartement de Microbiologie et Infectiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Canada.
Claudine RancourtDépartement de Microbiologie et Infectiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Canada.
Anne-Marie Mes-MassonCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM) and Institut du cancer de Montréal, Montreal, Canada.
Eran R AndrechekDepartment of Physiology, Michigan State University, East Lansing, Michigan, USA.
Peter M SiegelGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada. peter.siegel@mcgill.ca.
Centre Hospitalier de l’Université de Montréal · CAMichigan State University · USUniversité de Sherbrooke · CAMcGill University · CAMcGill University Health Centre · CA

Funding

The Role of E2F2 in HER2 Positive Breast CancerF99CA212221 · NCI · MICHIGAN STATE UNIVERSITY · PI RENNHACK, JONATHAN · 2016 to 2017
$85k
CIHR MOP-119401NCI NIH HHS F99 CA212221
6 · The paper itself

Abstract

backgroundThe Fos-related antigen 1 (FRA-1) transcription factor promotes tumor cell growth, invasion and metastasis. Phosphorylation of FRA-1 increases protein stability and function. We identify a novel signaling axis that leads to increased phosphorylation of FRA-1, increased extracellular matrix (ECM)-induced breast cancer cell invasion and is prognostic of poor outcome in patients with breast cancer.

methodsWhile characterizing five breast cancer cell lines derived from primary human breast tumors, we identified BRC-31 as a novel basal-like cell model that expresses elevated FRA-1 levels. We interrogated the functional contribution of FRA-1 and an upstream signaling axis in breast cancer cell invasion. We extended this analysis to determine the prognostic significance of this signaling axis in samples derived from patients with breast cancer.

resultsBRC-31 cells display elevated focal adhesion kinase (FAK), SRC and extracellular signal-regulated (ERK2) phosphorylation relative to luminal breast cancer models. Inhibition of this signaling axis, with pharmacological inhibitors, reduces the phosphorylation and stabilization of FRA-1. Elevated integrin α

conclusionsWe have identified a novel signaling axis that leads to phosphorylation and enhanced activity of FRA-1, a transcription factor that is emerging as an important modulator of breast cancer progression and metastasis.

Indexed as

Breast NeoplasmsExtracellular MatrixFemaleFos-Related Antigen 1HumansIntegrin alphaVbeta3MCF-7 CellsNeoplasm InvasivenessPhosphorylationProto-Oncogene Proteins c-fosReceptors, Urokinase Plasminogen ActivatorSignal TransductionUrokinase-Type Plasminogen ActivatorVitronectinFos-Related Antigen 1Integrin alphaVbeta3Proto-Oncogene Proteins c-fosReceptors, Urokinase Plasminogen ActivatorUrokinase-Type Plasminogen ActivatorVitronectinBreast cancerFRA-1IntegrinsInvasionuPAR

Identifiers

PMID29382358
PMCPMC5791353
OpenAlexW2789595663

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.