Evidence map›Paper›PMID 24409301›Full record

ArticlePloS one2014

PTK 7 is a transforming gene and prognostic marker for breast cancer and nodal metastasis involvement.

Silvia Gärtner, Angela Gunesch, Tatiana Knyazeva, Petra Wolf, Bernhard Högel, Wolfgang Eiermann, Axel Ullrich, Pjotr Knyazev, Beyhan Ataseven

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

46 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  5. Therapeutic advances of targeting receptor tyrosine kinases in cancer.Signal transduction and targeted therapy · 2024
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  19. Whole-Exome Sequencing Identifies a Novel Germline Variant inInternational journal of molecular sciences · 2022
    Article
  20. Review
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

9 authors at 3 institutions in 1 country.

Silvia GärtnerDepartment of Molecular Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.
Angela GuneschDepartment of Molecular Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.
Tatiana KnyazevaDepartment of Molecular Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.
Petra WolfInstitute for medical statistics and epidemiology, Klinikum rechts der Isar, Technical University, Munich, Germany.
Bernhard HögelDepartment of Pathology, Red Cross Hospital, Munich, Germany.
Wolfgang EiermannDepartment of Gynecology and Gynecologic Oncology, Interdisziplinäres Onkologisches Zentrum, Munich, Germany.
Axel UllrichDepartment of Molecular Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.
Pjotr KnyazevDepartment of Molecular Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.
Beyhan AtasevenDepartment of Gynecology and Obstetrics, Red Cross Hospital, Munich, Germany ; Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung, Essen, Germany.
Max Planck Institute of Biochemistry · DEKrankenhaus vom Roten Kreuz · DEKlinikum rechts der Isar · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein Tyrosin Kinase 7 (PTK7) is upregulated in several human cancers; however, its clinical implication in breast cancer (BC) and lymph node (LN) is still unclear. In order to investigate the function of PTK7 in mediating BC cell motility and invasivity, PTK7 expression in BC cell lines was determined. PTK7 signaling in highly invasive breast cancer cells was inhibited by a dominant-negative PTK7 mutant, an antibody against the extracellular domain of PTK7, and siRNA knockdown of PTK7. This resulted in decreased motility and invasivity of BC cells. We further examined PTK7 expression in BC and LN tissue of 128 BC patients by RT-PCR and its correlation with BC related genes like HER2, HER3, PAI1, MMP1, K19, and CD44. Expression profiling in BC cell lines and primary tumors showed association of PTK7 with ER/PR/HER2-negative (TNBC-triple negative BC) cancer. Oncomine data analysis confirmed this observation and classified PTK7 in a cluster with genes associated with agressive behavior of primary BC. Furthermore PTK7 expression was significantly different with respect to tumor size (ANOVA, p = 0.033) in BC and nodal involvement (ANOVA, p = 0.007) in LN. PTK7 expression in metastatic LN was related to shorter DFS (Cox Regression, p = 0.041). Our observations confirmed the transforming potential of PTK7, as well as its involvement in motility and invasivity of BC cells. PTK7 is highly expressed in TNBC cell lines. It represents a novel prognostic marker for BC patients and has potential therapeutic significance.

Indexed as

AdultAgedBiomarkers, TumorBreast NeoplasmsBreast Neoplasms, MaleCell Adhesion MoleculesCell Line, TumorCell MovementCell Transformation, NeoplasticCluster AnalysisFemaleGene ExpressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleBiomarkers, TumorCell Adhesion MoleculesPTK7 protein, humanReceptor Protein-Tyrosine Kinases

Identifiers

PMID24409301
PMCPMC3883666
OpenAlexW2067473404

What OpenQuestion holds

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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.