Evidence map›Paper›PMID 22187964›Full record

ReviewClinical science (London, England : 1979)2012

Axl-dependent signalling: a clinical update.

Vyacheslav A Korshunov

2 registry-linked trialsAbstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
3.5field-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.

NCT02424617 phase1 / phase2completednot on this mapstarted 2015, after this paper: background citation

A Multi-Center Open-Label Phase 1/2 Study of BGB324 in Combination With Erlotinib in Patients With Stage IIIb or Stage IV Non-Small Cell Lung Cancer

TypeinterventionalSponsorBerGenBio ASARan2015 to 2021Enrolled40ConditionsNon-Small Cell Lung CancerArmsErlotinib, Bemcentinib
NCT02488408 phase1 / phase2completednot on this mapstarted 2014, after this paper: background citation

A Phase Ib/II Multicenter Open-label Study of BGB324 as a Single Agent and in Combination With Cytarabine or Decitabine in Patients With Acute Myeloid Leukemia or as a Single Agent in Patients With Myelodysplastic Syndrome

TypeinterventionalSponsorBerGenBio ASARan2014 to 2022Enrolled122ConditionsAcute Myeloid Leukemia, Myelodysplastic SyndromesArmsBemcentinib, Cytarabine, Decitabine
3 · Its place in the literature

Who cites it

91 citing papers in PubMed, 154 citations in OpenAlex.

  1. Review
  2. ALDH1 and ALCAM as emerging biomarkers in personalized rectal cancer therapy.Arquivos brasileiros de cirurgia digestiva : ABCD = Brazilian archives of digestive surgery · 2026
    Article
  3. Article
  4. Article
  5. Recent advances in TAM mechanisms in lung diseases.Journal of translational medicine · 2025
    Review
  6. AXL signaling in cancer: from molecular insights to targeted therapies.Signal transduction and targeted therapy · 2025
    Review
  7. Article
  8. Review
  9. Small Molecule Tyrosine Kinase Inhibitors (TKIs) for Glioblastoma Treatment.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Article
  12. International journal of molecular sciences · 2023
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

31 more citing papers are in PubMed but not listed here.

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

1 author at 1 institution in 1 country.

Vyacheslav A KorshunovDepartment of Medicine, Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA. Slava_Korshunov@URMC.rochester.edu
University of Rochester · US

Funding

The Role of Immune Response in Vascular Dysfunction in HypertensionR01HL105623 · NHLBI · UNIVERSITY OF ROCHESTER · PI KORSHUNOV, VYACHESLAV A · 2011 to 2015
$1.5M
NHLBI NIH HHS HL105623NHLBI NIH HHS R01 HL105623
6 · The paper itself

Abstract

Axl is a receptor tyrosine kinase that was originally cloned from cancer cells. Axl belongs to the TAM (Tyro3, Axl and Mertk) family of receptor tyrosine kinases. Gas6 (growth-arrest-specific protein 6) is a ligand for Axl. Activation of Axl protects cells from apoptosis, and increases migration, aggregation and growth through multiple downstream pathways. Up-regulation of the Gas6/Axl pathway is more evident in pathological conditions compared with normal physiology. Recent advances in Axl receptor biology are summarized in the present review. The emphasis is given to translational aspects of Axl-dependent signalling under pathological conditions. In particular, inhibition of Axl reduces tumorigenesis and prevents metastasis as well. Axl-dependent signals are important for the progression of cardiovascular diseases. In contrast, deficiency of Axl in innate immune cells contributes to the pathogenesis of autoimmune disorders. Current challenges in Axl biology are related to the functional interactions of Axl with other members of the TAM family or other tyrosine kinases, mechanisms of ligand-independent activation, inactivation of the receptor and cell-cell interactions (with respect to immune cells) in chronic diseases.

Indexed as

Signal TransductionAnimalsAxl Receptor Tyrosine KinaseCardiovascular DiseasesHumansImmune System DiseasesNeoplasmsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAXL protein, humanAxl Receptor Tyrosine KinaseProto-Oncogene ProteinsReceptor Protein-Tyrosine Kinases

Identifiers

PMID22187964
PMCPMC3609429
OpenAlexW2128841304

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.