Evidence map›Paper›PMID 39468753›Full record

ReviewThe oncologist2025

Therapeutic targeting of the protein tyrosine kinase-7 in cancer: an overview.

Kim Mottard, Julie Cokaiko, Bernard Rogister, Virginie Neirinckx

Abstract readReview
In one paragraph

Review in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cytotoxicity ofEJNMMI radiopharmacy and chemistry · 2025
    Article
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

4 authors.

Kim MottardLaboratory of Nervous System Diseases and Therapy, GIGA Institute, University of Liège, 4000 Liège, Belgium.ORCID 0009-0001-7422-7887
Julie CokaikoLaboratory of Nervous System Diseases and Therapy, GIGA Institute, University of Liège, 4000 Liège, Belgium.
Bernard RogisterLaboratory of Nervous System Diseases and Therapy, GIGA Institute, University of Liège, 4000 Liège, Belgium.
Virginie NeirinckxLaboratory of Nervous System Diseases and Therapy, GIGA Institute, University of Liège, 4000 Liège, Belgium.ORCID 0000-0002-9050-6579

Funding

University of Liège and the F.R.S.-FNRS-Télévie 7.4581.22
6 · The paper itself

Abstract

The protein tyrosine kinase-7 (PTK7) is an evolutionarily conserved transmembrane receptor that has emerged as a potential therapeutic target for human tumors. PTK7 is a pseudokinase that is involved in the modulation of the Wnt signaling pathway through interactions with other receptors. These interactions result in targeted gene activation that regulates cell polarity, migration, and proliferation during embryogenesis. Aside of this role during development, PTK7 has been shown as overexpressed in numerous cancers including colon carcinoma, leukemia, neuroblastoma, hepatoma, and ovarian cancer. The activity of PTK7 and the direct correlation with poor prognosis have fostered preclinical investigations and phase I clinical trials, aiming at inhibiting PTK7 and inducing antitumoral effects. In this review, we provide an exhaustive overview of the diverse approaches that use PTK7 as a new molecular target for cancer therapy in different tumor types. We discuss current therapies and future strategies including chimeric antigen receptor-T cells, antibody-drug conjugates, aptamers, based on up-to-date literature and ongoing research progress.

Indexed as

Molecular Targeted TherapyNeoplasmsReceptor Protein-Tyrosine KinasesCell Adhesion MoleculesHumansCell Adhesion MoleculesPTK7 protein, humanReceptor Protein-Tyrosine Kinasesantibody-drug conjugateaptamercancer therapyCAR-T cellPTK7targeted therapy

Identifiers

PMID39468753
PMCPMC12395136

What OpenQuestion holds

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LicenceCC BY-NC
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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.