Evidence map›Paper›PMID 33377205›Full record

ReviewCancer science2021

Discoidin domain receptors orchestrate cancer progression: A focus on cancer therapies.

Yuan Gao, Jiuli Zhou, Jin Li

Open access · goldAbstract readReview
In one paragraph

Review in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Control of Schwann Cell Myelination by DDR1 Receptor Tyrosine Kinase.International journal of molecular sciences · 2026
    Article
  4. Article
  5. Article
  6. Drug repositioning of regorafenib for renal cell carcinoma identifiesThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
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  13. Review
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  15. Article
  16. Article
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  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

3 authors at 2 institutions in 1 country.

Yuan GaoTongji University School of Medicine, Shanghai, China.ORCID https://orcid.org/0000-0003-3227-2310
Jiuli ZhouDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Jin LiDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.ORCID https://orcid.org/0000-0001-5523-0055
Shanghai East Hospital · CNTongji University · CN

Funding

Outstanding Clinical Discipline Project of Shanghai Pudong PWYgy2018-02Shanghai Sailing Program 20YF1453300
6 · The paper itself

Abstract

Discoidin domain receptors (DDR), including DDR1 and DDR2, are special types of the transmembrane receptor tyrosine kinase superfamily. DDR are activated by binding to the triple-helical collagen and, in turn, DDR can activate signal transduction pathways that regulate cell-collagen interactions involved in multiple physiological and pathological processes such as cell proliferation, migration, apoptosis, and cytokine secretion. Recently, DDR have been found to contribute to various diseases, including cancer. In addition, aberrant expressions of DDR have been reported in various human cancers, which indicates that DDR1 and DDR2 could be new targets for cancer treatment. Considerable effort has been made to design DDR inhibitors and several molecules have shown therapeutic effects in pre-clinical models. In this article, we review the recent literature on the role of DDR in cancer progression, the development status of DDR inhibitors, and the clinical potential of targeting DDR in cancer therapies.

Indexed as

AnimalsAntineoplastic AgentsCarcinogenesisCell Line, TumorDiscoidin Domain ReceptorsDisease Models, AnimalDisease ProgressionDrug Screening Assays, AntitumorHumansMiceMice, KnockoutMolecular Targeted TherapyNeoplasmsProtein Kinase InhibitorsAntineoplastic AgentsDiscoidin Domain ReceptorsProtein Kinase Inhibitorsantagonists and inhibitorsdiscoidin domain receptorsneoplasmsreceptor protein-tyrosine kinasestherapeutic uses

Identifiers

PMID33377205
PMCPMC7935774
OpenAlexW3114299819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.