Evidence map›Paper›PMID 25962058›Full record

ArticlePloS one2015

Overexpression of the Promigratory and Prometastatic PTK7 Receptor Is Associated with an Adverse Clinical Outcome in Colorectal Cancer.

Anne-Catherine Lhoumeau, Sébastien Martinez, Jean-Marie Boher, Geneviève Monges, Rémy Castellano, Armelle Goubard, Marie Doremus, Flora Poizat, Bernard Lelong, Cécile de Chaisemartin and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

35 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Therapeutic advances of targeting receptor tyrosine kinases in cancer.Signal transduction and targeted therapy · 2024
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  15. Whole-Exome Sequencing Identifies a Novel Germline Variant inInternational journal of molecular sciences · 2022
    Article
  16. Review
  17. First-in-Human Study of PF-06647020 (Cofetuzumab Pelidotin), an Antibody-Drug Conjugate Targeting Protein Tyrosine Kinase 7, in Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
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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

17 authors at 4 institutions in 1 country.

Anne-Catherine LhoumeauCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France; Department of Biopathology, Institut Paoli-Calmettes, Marseille, France.
Sébastien MartinezCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Jean-Marie BoherInstitut Paoli-Calmettes, Marseille, F-13009, France; Department of Biostatistics, Institut Paoli-Calmettes, Marseille, France.
Geneviève MongesInstitut Paoli-Calmettes, Marseille, F-13009, France; Department of Biopathology, Institut Paoli-Calmettes, Marseille, France.
Rémy CastellanoCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Armelle GoubardCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Marie DoremusCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Flora PoizatInstitut Paoli-Calmettes, Marseille, F-13009, France; Department of Biopathology, Institut Paoli-Calmettes, Marseille, France.
Bernard LelongInstitut Paoli-Calmettes, Marseille, F-13009, France; Department of Surgical Oncology, Institut Paoli-Calmettes, Marseille, France.
Cécile de ChaisemartinInstitut Paoli-Calmettes, Marseille, F-13009, France; Department of Surgical Oncology, Institut Paoli-Calmettes, Marseille, France.
Florence BardinCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Patrice ViensCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France; Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.
Jean-Luc RaoulCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France; Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.
Thomas PrebetCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
Michel Aurrand-LionsCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Jean-Paul BorgCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France.
Anthony GonçalvesCRCM, Team Cell Polarity, Cell signalling and Cancer "Equipe labellisée Ligue Contre le Cancer", Inserm, U1068, Marseille, F-13009, France; Institut Paoli-Calmettes, Marseille, F-13009, France; Aix-Marseille Université, Marseille, F-13284, France; CNRS, UMR7258, F-13009, Marseille, France; Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.
Institut Paoli-Calmettes · FRCentre National de la Recherche Scientifique · FRInserm · FRLa Ligue Contre le Cancer · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biomarkers and novel therapeutic targets are urgently needed in colorectal cancer (CRC). The pseudo tyrosine kinase receptor 7 (PTK7) is involved in planar cell polarity and it is deregulated in various malignancies, including CRC. Yet, little is known about its protein expression in human CRC, or about a possible correlation of its expression with clinical endpoints. Using a clinically annotated Tissue MicroArray (TMA) produced from from 192 consecutive CRC patients treated by initial surgery, we examined PTK7 expression by immunohistochemistry in tumoral tissue and matched normal mucosae, and correlated its expression with clinico-pathological features and patient outcome. PTK7 depletion by specific shRNA in HCT116 and HCT15 CRC cell lines was found to affect cell proliferation, resistance to drugs and cell migration. Tumor growth and metastatic phenotype were investigated in vivo using a xenograft mouse model of CRC cells with modulated expression of PTK7 levels. PTK7 was significantly up-regulated in CRC tissue as compared to matched healthy mucosae, and significant overexpression was found in 34% of patients. PTK7 overexpression was significantly associated with a reduced metastasis-free survival in non-metastatic patients. In HCT116 and HCT15 cells, shRNA PTK7 reduced migration but did not affect cell proliferation and resistance to drugs. In a xenograft mouse of HCT15 cells, downregulation of PTK7 led to reduced tumor growth, whereas its overexpression in PTK7-negative cancer cells led to increased metastatic events. PTK7 expression thus represents a potential prognostic biomarker and a novel therapeutic target in CRC.

Indexed as

Gene ExpressionAnimalsCell Adhesion MoleculesCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDisease Models, AnimalDown-RegulationDrug Resistance, NeoplasmFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHeterograftsHumansMaleCell Adhesion MoleculesPTK7 protein, humanReceptor Protein-Tyrosine KinasesRNA, Small Interfering

Identifiers

PMID25962058
PMCPMC4427440
OpenAlexW393131535

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.