Evidence map›Paper›PMID 30361264›Full record

ArticleEMBO molecular medicine2018

EGFR is required for FOS-dependent bone tumor development via RSK2/CREB signaling.

Markus Linder, Elisabeth Glitzner, Sriram Srivatsa, Latifa Bakiri, Kazuhiko Matsuoka, Parastoo Shahrouzi, Monika Dumanic, Philipp Novoszel, Thomas Mohr, Oliver Langer and 4 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Therapeutic Effects ofInternational journal of molecular sciences · 2026
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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

14 authors at 5 institutions in 2 countries.

Markus LinderDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Elisabeth GlitznerDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Sriram SrivatsaDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Latifa BakiriSpanish National Cancer Research Center (CNIO), Madrid, Spain.
Kazuhiko MatsuokaSpanish National Cancer Research Center (CNIO), Madrid, Spain.
Parastoo ShahrouziDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Monika DumanicDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.
Philipp NovoszelDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Thomas MohrDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Oliver LangerDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.
Thomas WanekCenter for Health & Bioresources, AIT Austrian Institute of Technology GmbH, Seibersdorf, Austria.
Markus MitterhauserDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.
Erwin F WagnerSpanish National Cancer Research Center (CNIO), Madrid, Spain.
Maria SibiliaDepartment of Medicine I, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria Sibilia-Office@meduniwien.ac.at.ORCID 0000-0001-6129-5613
Comprehensive Cancer Center Vienna · ATSpanish National Cancer Research Centre · ESAustrian Institute of Technology · ATLudwig Boltzmann Institute Applied Diagnostics · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is a rare tumor of the bone occurring mainly in young adults accounting for 5% of all childhood cancers. Because of the limited therapeutic options, there has been no survival improvement for OS patients in the past 40 years. The epidermal growth factor receptor (EGFR) is highly expressed in OS; however, its clinical relevance is unclear. Here, we employed an autochthonous c-Fos-dependent OS mouse model (H2

Indexed as

Signal TransductionAnimalsBone NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationCell SurvivalCyclic AMP Response Element-Binding ProteinErbB ReceptorsGene DeletionHumansLigandsMiceMitogen-Activated Protein KinasesOsteoblastsOsteosarcomaCyclic AMP Response Element-Binding ProteinErbB ReceptorsLigandsMitogen-Activated Protein KinasesProto-Oncogene Proteins c-fosribosomal protein S6 kinase, 90kDa, polypeptide 3Ribosomal Protein S6 Kinases, 90-kDac‐FosCREBepidermal growth factor receptorosteosarcomaRSK2

Identifiers

PMID30361264
PMCPMC6220323
OpenAlexW2898520420

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.