Evidence map›Paper›PMID 25906745›Full record

ArticleOncotarget2015

ERG deregulation induces IGF-1R expression in prostate cancer cells and affects sensitivity to anti-IGF-1R agents.

Caterina Mancarella, Irene Casanova-Salas, Ana Calatrava, Selena Ventura, Cecilia Garofalo, José Rubio-Briones, Vera Magistroni, Maria Cristina Manara, José Antonio López-Guerrero, Katia Scotlandi

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 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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  11. Height, Obesity, and the Risk ofCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2018
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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 3 institutions in 2 countries.

Caterina MancarellaCRS Development of Biomolecular Therapies, Experimental Oncology Lab, Rizzoli Orthopaedic Institute, Bologna, Italy.
Irene Casanova-SalasLaboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Ana CalatravaDepartment of Pathology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Selena VenturaCRS Development of Biomolecular Therapies, Experimental Oncology Lab, Rizzoli Orthopaedic Institute, Bologna, Italy.
Cecilia GarofaloCRS Development of Biomolecular Therapies, Experimental Oncology Lab, Rizzoli Orthopaedic Institute, Bologna, Italy.
José Rubio-BrionesDepartment of Urology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Vera MagistroniDepartment of Health Sciences, University of Milano-Bicocca, Monza, Italy.
Maria Cristina ManaraCRS Development of Biomolecular Therapies, Experimental Oncology Lab, Rizzoli Orthopaedic Institute, Bologna, Italy.
José Antonio López-GuerreroLaboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Katia ScotlandiCRS Development of Biomolecular Therapies, Experimental Oncology Lab, Rizzoli Orthopaedic Institute, Bologna, Italy.
Istituto Ortopedico Rizzoli · ITFundación Instituto Valenciano de Oncología · ESUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying patients who may benefit from targeted therapy is an urgent clinical issue in prostate cancer (PCa). We investigated the molecular relationship between TMPRSS2-ERG (T2E) fusion gene and insulin-like growth factor receptor (IGF-1R) to optimize the use of IGF-1R inhibitors.IGF-1R was analyzed in cell lines and in radical prostatectomy specimens in relation to T2E status. ERG binding to IGF-1R promoter was evaluated by chromatin immunoprecipitation (ChIP). Sensitivity to anti-IGF-1R agents was evaluated alone or in combination with anti-androgen abiraterone acetate in vitro at basal levels or upon ERG modulation.IGF-1R analysis performed in PCa cells or clinical samples showed that T2E expression correlated with higher IGF-1R expression at mRNA and protein levels. Genetic modulation of ERG directly affected IGF-1R protein levels in vitro. ChIP analysis showed that ERG binds IGF-1R promoter and that promoter occupancy is higher in T2E-positive cells. IGF-1R inhibition was more effective in cell lines expressing the fusion gene and combination of IGF-1R inhibitors with abiraterone acetate produced synergistic effects in T2E-expressing cells.Here, we provide the rationale for use of T2E fusion gene to select PCa patients for anti-IGF-1R treatments. The combination of anti-IGF-1R-HAbs with an anti-androgen therapy is strongly advocated for patients expressing T2E.

Indexed as

Abiraterone AcetateAndrogen AntagonistsAntineoplastic AgentsBiomarkers, TumorCell Line, TumorDNA-Binding ProteinsHumansMalePromoter Regions, GeneticProstateProstatic NeoplasmsProtein BindingReceptor, IGF Type 1Recombinant Fusion ProteinsSerine EndopeptidasesTrans-ActivatorsAbiraterone AcetateAndrogen AntagonistsAntineoplastic AgentsBiomarkers, TumorDNA-Binding ProteinsERG protein, humanReceptor, IGF Type 1Recombinant Fusion ProteinsSerine EndopeptidasesTMPRSS2 protein, humanTrans-ActivatorsTranscriptional Regulator ERGanti-IGF-1R agentsETS fusion genesinsulin-like growth factor receptor 1prostate cancer

Identifiers

PMID25906745
PMCPMC4599293
OpenAlexW1889643605

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.