Evidence map›Paper›PMID 26356564›Full record

ArticleOncotarget2015

Novel Axl-driven signaling pathway and molecular signature characterize high-grade ovarian cancer patients with poor clinical outcome.

Katia Rea, Patrizia Pinciroli, Marialuisa Sensi, Federica Alciato, Brigitte Bisaro, Ludmila Lozneanu, Francesco Raspagliesi, Floriana Centritto, Sara Cabodi, Paola Defilippi and 3 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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  9. TAM receptors, Phosphatidylserine, inflammation, and Cancer.Cell communication and signaling : CCS · 2019
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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

13 authors at 4 institutions in 3 countries.

Katia ReaUnit of Molecular Therapies, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Patrizia PinciroliFunctional Genomics and Bioinformatics Core Facility, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Marialuisa SensiFunctional Genomics and Bioinformatics Core Facility, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Federica AlciatoDepartment of Traslational Medicine, Università degli Studi del Piemonte Orientale, Novara, Italy.
Brigitte BisaroDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Italy.
Ludmila LozneanuDepartment of Morphofunctional Sciences, Histology, Morphopatology, "Grigore T. Popa" University of Medicine and Pharmacy, Iassy, Romania.
Francesco RaspagliesiGynecology Oncology Unit, Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Floriana CentrittoFunctional Genomics and Bioinformatics Core Facility, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Sara CabodiDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Italy.
Paola DefilippiDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Italy.
Gian Carlo AvanziDepartment of Traslational Medicine, Università degli Studi del Piemonte Orientale, Novara, Italy.
Silvana CanevariFunctional Genomics and Bioinformatics Core Facility, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Antonella TomassettiUnit of Molecular Therapies, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITUniversity of Turin · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITMorpho (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-grade epithelial ovarian cancer (HGEOC) is a clinically diverse and molecularly heterogeneous disease comprising subtypes with distinct biological features and outcomes. The receptor tyrosine kinases, expressed by EOC cells, and their ligands, present in the microenvironment, activate signaling pathways, which promote EOC cells dissemination. Herein, we established a molecular link between the presence of Gas6 ligand in the ascites of HGEOCs, the expression and activation of its receptor Axl in ovarian cancer cell lines and biopsies, and the progression of these tumors. We demonstrated that Gas6/Axl signalling converges on the integrin β3 pathway in the presence of the adaptor protein p130Cas, thus inducing tumor cell adhesion to the extracellular matrix and invasion. Accordingly, Axl and p130Cas were significantly co-expressed in HGEOC samples. Clinically, we identified an Axl-associated signature of 62 genes able to portray the HGEOCs with the shortest overall survival. These data biologically characterize a group of HGEOCs and could help guide a more effective therapeutic approach to be taken for these patients.

Indexed as

Gene Expression ProfilingAscitesAxl Receptor Tyrosine KinaseBiomarkers, TumorBiopsyCarcinoma, Ovarian EpithelialCell AdhesionCell Line, TumorCrk-Associated Substrate ProteinExtracellular MatrixFemaleGene Regulatory NetworksGrowth Arrest-Specific Protein 6HumansIntegrin beta3Intercellular Signaling Peptides and ProteinsAXL protein, humanAxl Receptor Tyrosine KinaseBCAR1 protein, humanBiomarkers, TumorCrk-Associated Substrate ProteinGrowth Arrest-Specific Protein 6Integrin beta3Intercellular Signaling Peptides and ProteinsITGB3 protein, humanProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAxlextracellular matrixGas6ovarian cancerp130Cas

Identifiers

PMID26356564
PMCPMC4741573
OpenAlexW2194492326

What OpenQuestion holds

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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.