Evidence map›Paper›PMID 27081701›Full record

ArticleOncotarget2016

MERTK as a novel therapeutic target in head and neck cancer.

Anne von Mässenhausen, Christine Sanders, Britta Thewes, Mario Deng, Angela Queisser, Wenzel Vogel, Glen Kristiansen, Stefan Duensing, Andreas Schröck, Friedrich Bootz and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. MERTK Inhibition as a Targeted Novel Cancer Therapy.International journal of molecular sciences · 2024
    Review
  2. Article
  3. New insights into RAS in head and neck cancer.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
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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

15 authors at 5 institutions in 2 countries.

Anne von MässenhausenSection of Prostate Cancer Research, University Hospital of Bonn, Bonn, Germany.
Christine SandersSection of Prostate Cancer Research, University Hospital of Bonn, Bonn, Germany.
Britta ThewesSection of Prostate Cancer Research, University Hospital of Bonn, Bonn, Germany.
Mario DengPathology of The University Hospital of Luebeck, Luebeck, Germany.
Angela QueisserSection of Prostate Cancer Research, University Hospital of Bonn, Bonn, Germany.
Wenzel VogelPathology of The University Hospital of Luebeck, Luebeck, Germany.
Glen KristiansenInstitute of Pathology, University Hospital of Bonn, Bonn, Germany.
Stefan DuensingDepartment of Urology, University of Heidelberg, Heidelberg, Germany.
Andreas SchröckCenter for Integrated Oncology Cologne/Bonn, University Hospital of Bonn, Bonn, Germany.
Friedrich BootzCenter for Integrated Oncology Cologne/Bonn, University Hospital of Bonn, Bonn, Germany.
Peter BrossartCenter for Integrated Oncology Cologne/Bonn, University Hospital of Bonn, Bonn, Germany.
Jutta KirfelInstitute of Pathology, University Hospital of Bonn, Bonn, Germany.
Lynn HeasleyDepartment of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Johannes BrägelmannSection of Prostate Cancer Research, University Hospital of Bonn, Bonn, Germany.
Sven PernerPathology of The University Hospital of Luebeck, Luebeck, Germany.
University Hospital Bonn · DEResearch Center Borstel - Leibniz Lung Center · DEHeidelberg University · DEUniversity of Colorado Anschutz Medical Campus · USUniversity of Lübeck · DE

Funding

An FGFR1 oncogene driver pathway in head and neck cancerI01BX001994 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI HEASLEY, LYNN E · 2014 to 2017
–
BLRD VA I01 BX001994
6 · The paper itself

Abstract

Although head and neck cancer (HNSCC) is the sixth most common tumor entity worldwide therapy options remain limited leading to 5-year survival rates of only 50 %. MERTK is a promising therapeutic target in several tumor entities, however, its role in HNSCC has not been described yet. The aim of our study was to investigate the biological significance of MERTK and to evaluate its potential as a novel therapeutic target in this dismal tumor entity. In two large HNSCC cohorts (n=537 and n=520) we found that MERTK is overexpressed in one third of patients. In-vitro, MERTK overexpression led to increased proliferation, migration and invasion whereas MERTK inhibition with the small molecule inhibitor UNC1062 or MERTK knockdown reduced cell motility via the small GTPase RhoA.Taken together, we are the first to show that MERTK is frequently overexpressed in HNSCC and plays an important role in tumor cell motility. It might therefore be a potential target for selected patients suffering from this dismal tumor entity.

Indexed as

AdolescentAdultAgedAged, 80 and overAntineoplastic AgentsBiomarkers, TumorCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationChildc-Mer Tyrosine KinaseDose-Response Relationship, DrugFemaleGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticAntineoplastic AgentsBiomarkers, Tumorc-Mer Tyrosine KinaseMERTK protein, humanMorpholinesProtein Kinase InhibitorsrhoA GTP-Binding ProteinRHOA protein, humanSulfonamidesUNC1062head and neck cancerMERTKtargeted therapy

Identifiers

PMID27081701
PMCPMC5078043
OpenAlexW2340124689

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.