Evidence map›Paper›PMID 35952318›Full record

ArticleJCO precision oncology2022

SRC Family Kinase Inhibition Targets YES1 and YAP1 as Primary Drivers of Lung Cancer and as Mediators of Acquired Resistance to ALK and Epidermal Growth Factor Receptor Inhibitors.

Hiroki Sato, Daisuke Kubota, Huan Qiao, Achim Jungbluth, Natasha Rekhtman, Adam J Schoenfeld, Helena A Yu, Gregory J Riely, Shinichi Toyooka, Christine M Lovly and 3 more

Open access · hybridAbstract read
In one paragraph

Article in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Emerging Roles of YES1 in Cancer: The Putative Target in Drug Resistance.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Review
  10. 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

13 authors at 3 institutions in 2 countries.

Hiroki SatoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Daisuke KubotaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Huan QiaoVanderbilt Ingram Cancer Center and Department of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN.
Achim JungbluthDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Natasha RekhtmanDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-5801-3144
Adam J SchoenfeldDivision of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-2644-1416
Helena A YuDivision of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-0377-9510
Gregory J RielyDivision of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-5357-4313
Shinichi ToyookaDepartment of Thoracic, Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.ORCID 0000-0002-7588-6745
Christine M LovlyVanderbilt Ingram Cancer Center and Department of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0002-3641-6361
Paul PaikDivision of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-9464-3984
Marc LadanyiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-9055-7213
Pang-Dian FanDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-7968-7516
Memorial Sloan Kettering Cancer Center · USVanderbilt University Medical Center · USOkayama University · JP

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The Role of Focal Oncogene Amplifications in Lung CancerP01CA129243 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Marc Ladanyi · 2007 to 2026
$31.2M
NCI NIH HHS P01 CA129243NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeThe identification of novel oncogenic driver alterations and novel mechanisms of acquired resistance (AR) is the key for further development of personalized therapy. The current study investigates the potential role of

methodsModels of ectopic expression were established and characterized for YES1 and YAP1 in human bronchial epithelial cells and

resultsWe report response to SRC family kinase (SFK) inhibition in a patient whose lung cancer exhibited

conclusionOur results demonstrate the therapeutic potential of SFK inhibition in primary tumorigenesis and AR driven by YES1/YAP1 signaling.

Indexed as

Adenocarcinoma of LungLung NeoplasmsAnaplastic Lymphoma KinaseCarcinogenesisErbB ReceptorsHumansProtein Kinase InhibitorsProto-Oncogene Proteins c-yessrc-Family KinasesYAP-Signaling ProteinsAnaplastic Lymphoma KinaseErbB ReceptorsProtein Kinase InhibitorsProto-Oncogene Proteins c-yessrc-Family KinasesYAP1 protein, humanYAP-Signaling ProteinsYES1 protein, human

Identifiers

PMID35952318
PMCPMC9384924
OpenAlexW4291000429

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.