Evidence map›Paper›PMID 29701112›Full record

ReviewCell adhesion & migration2018

Multitasking discoidin domain receptors are involved in several and specific hallmarks of cancer.

Elodie Henriet, Margaux Sala, Aya Abou Hammoud, Adjanie Tuariihionoa, Julie Di Martino, Manon Ros, Frédéric Saltel

Abstract readReview
In one paragraph

Review in Cell adhesion & migration, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–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

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Genotype-Based Molecular Mechanisms in Alport Syndrome.Journal of the American Society of Nephrology : JASN · 2025
    Review
  8. Article
  9. Discoid Domain Receptors Signaling in Macrophages-Mediated Diseases.International journal of general medicine · 2025
    Review
  10. Therapeutic advances of targeting receptor tyrosine kinases in cancer.Signal transduction and targeted therapy · 2024
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

7 authors.

Elodie Henrieta INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.
Margaux Salaa INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.
Aya Abou Hammouda INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.
Adjanie Tuariihionoaa INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.
Julie Di Martinoa INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.
Manon Rosa INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.
Frédéric Saltela INSERM, UMR1053, BaRITOn Bordeaux Research in Translational Oncology , Bordeaux , France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Discoidin domain receptors, DDR1 and DDR2, are two members of collagen receptor family that belong to tyrosine kinase receptor subgroup. Unlike other matrix receptor-like integrins, these collagen receptors have not been extensively studied. However, more and more studies are focusing on their involvement in cancer. These two receptors are present in several subcellular localizations such as intercellular junction or along type I collagen fibers. Consequently, they are involved in multiple cellular functions, for instance, cell cohesion, proliferation, adhesion, migration and invasion. Furthermore, various signaling pathways are associated with these multiple functions. In this review, we highlight and characterize hallmarks of cancer in which DDRs play crucial roles. We discuss recent data from studies that demonstrate the involvement of DDRs in tumor proliferation, cancer mutations, drug resistance, inflammation, neo-angiogenesis and metastasis. DDRs could be potential targets in cancer and we conclude this review by discussing the different ways to inhibits them.

Indexed as

AnimalsDiscoidin Domain ReceptorsDrug Resistance, NeoplasmHumansModels, BiologicalNeoplasmsSignal TransductionDiscoidin Domain Receptorsfenestraelivers sinusoidal endothelial cells (LSEC)STED microscopy

Identifiers

PMID29701112
PMCPMC6411096

What OpenQuestion holds

Textmetadata
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.