Evidence map›Paper›PMID 31911857›Full record

ArticleAmerican journal of cancer research2019

The potential role of YAP in Axl-mediated resistance to EGFR tyrosine kinase inhibitors.

Sarah Saab, Olin Shih-Shin Chang, Kentaro Nagaoka, Mien-Chie Hung, Hirohito Yamaguchi

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

26 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Cancers · 2026
    Article
  4. Review
  5. Article
  6. Self-Assembled Multilayered Concentric Supraparticle Architecture.Advanced materials (Deerfield Beach, Fla.) · 2025
    Article
  7. Article
  8. AXL signaling in cancer: from molecular insights to targeted therapies.Signal transduction and targeted therapy · 2025
    Review
  9. YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate.International journal of molecular sciences · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. MRCK as a Potential Target for Claudin-Low Subtype of Breast Cancer.International journal of biological sciences · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

5 authors at 3 institutions in 3 countries.

Sarah SaabCancer Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation PO Box 34110, Doha, Qatar.
Olin Shih-Shin ChangDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Unit 108, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Kentaro NagaokaLaboratory of Veterinary Physiology, Department of Veterinary Medicine, Tokyo University of Agriculture and Technology Fuchu, Tokyo 183-8509, Japan.
Mien-Chie HungDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Unit 108, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Hirohito YamaguchiCancer Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation PO Box 34110, Doha, Qatar.
Asia University · TWThe University of Texas MD Anderson Cancer Center · USTokyo University of Agriculture and Technology · JP

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Yes-associated protein (YAP) is a transcription co-regulator downstream of the Hippo pathway, and plays a critical role in cancer. Although YAP regulation in the canonical Hippo pathway is well established, the Hippo-independent regulation of YAP is not well explored. Here, we showed the possible new mechanism of YAP regulation by the receptor tyrosine kinase Axl. Co-immunoprecipitation and Western blot analysis demonstrated the interaction between YAP and Axl, which was enhanced by Axl ligand Growth Arrest Specific 6 (GAS6) stimulation. Furthermore, we found that YAP is phosphorylated at tyrosine residues by GAS6 stimulation

Indexed as

Axllung cancerresistancetyrosine kinase inhibitorYAP

Identifiers

PMID31911857
PMCPMC6943358
OpenAlexW3003768662

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.