Evidence map›Paper›PMID 29856687›Full record

ArticleCancer biology & therapy2018

Induction of anaplastic lymphoma kinase (ALK) as a novel mechanism of EGFR inhibitor resistance in head and neck squamous cell carcinoma patient-derived models.

Xiaoming Ouyang, Ashley Barling, Aletha Lesch, Jeffrey W Tyner, Gabrielle Choonoo, Christina Zheng, Sophia Jeng, Toni M West, Daniel Clayburgh, Sara A Courtneidge and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Xiaoming Ouyanga Department of Dermatology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.ORCID 0000-0002-6632-3190
Ashley Barlinga Department of Dermatology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Aletha Lescha Department of Dermatology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Jeffrey W Tynerb Department of Cell , Developmental & Cancer Biology, Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Gabrielle Choonood Division of Bioinformatics and Computational Biology , Department of Medical Informatics & Clinical Epidemiology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Christina Zhengd Division of Bioinformatics and Computational Biology , Department of Medical Informatics & Clinical Epidemiology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Sophia Jengd Division of Bioinformatics and Computational Biology , Department of Medical Informatics & Clinical Epidemiology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Toni M Westf Department of Pharmacology , University of California at Davis , 451 Health Science Dr., Davis , California.
Daniel Clayburghg Department of Otolaryngology-Head and Neck Surgery , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Sara A Courtneidgeb Department of Cell , Developmental & Cancer Biology, Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Shannon K McWeeneyd Division of Bioinformatics and Computational Biology , Department of Medical Informatics & Clinical Epidemiology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Molly Kulesz-Martina Department of Dermatology , Oregon Health & Science University , 3181 SW Sam Jackson Park Rd., Portland , Oregon.
Oregon Health & Science University · USUniversity of California, Davis · US

Funding

Oregon Clinical and Translational Research Institute - The National COVID Cohort Collaborative (N3C)UL1TR002369 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Cynthia D Morris, Christopher G. Slatore · 2017 to 2026
$78.4M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Grace B Gill · 1997 to 2026
$60.5M
Illuminating molecular targetable pathways in HNSCCR01CA192405 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MCWEENEY, SHANNON K. · 2015 to 2019
$2.5M
Microenvironmental impact on HNSCC response to targeted therapyR21CA180576 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI KULESZ-MARTIN, MOLLY F. · 2013 to 2014
$363k
NCATS NIH HHS UL1 TR002369NCI NIH HHS P30 CA069533NCI NIH HHS R01 CA192405NCI NIH HHS R21 CA180576
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) currently only has one FDA-approved cancer intrinsic targeted therapy, the epidermal growth factor receptor (EGFR) inhibitor cetuximab, to which only approximately 10% of tumors are sensitive. In order to extend therapy options, we subjected patient-derived HNSCC cells to small-molecule inhibitor and siRNA screens, first, to find effective combination therapies with an EGFR inhibitor, and second, to determine a potential mechanistic basis for repurposing the FDA approved agents for HNSCC. The combinations of EGFR inhibitor with anaplastic lymphoma kinase (ALK) inhibitors demonstrated synergy at the highest ratio in our cohort, 4/8 HNSCC patients' derived tumor cells, and this corresponded with an effectiveness of siRNA targeting ALK combined with the EGFR inhibitor gefitinib. Co-targeting EGFR and ALK decreased HNSCC cell number and colony formation ability and increased annexin V staining. Because ALK expression is low and ALK fusions are infrequent in HNSCC, we hypothesized that gefitinib treatment could induce ALK expression. We show that ALK expression was induced in HNSCC patient-derived cells both in 2D and 3D patient-derived cell culture models, and in patient-derived xenografts in mice. Four different ALK inhibitors, including two (ceritinib and brigatinib) FDA approved for lung cancer, were effective in combination with gefitinib. Together, we identified induction of ALK by EGFR inhibitor as a novel mechanism potentially relevant to resistance to EGFR inhibitor, a high ratio of response of HNSCC patient-derived tumor cells to a combination of ALK and EGFR inhibitors, and applicability of repurposing ALK inhibitors to HNSCC that lack ALK aberrations.

Indexed as

Anaplastic Lymphoma KinaseAnimalsAntineoplastic AgentsCell Line, TumorDisease Models, AnimalDrug Resistance, NeoplasmErbB ReceptorsGene Expression Regulation, NeoplasticHumansMicePhosphorylationProtein Kinase InhibitorsRNA InterferenceRNA, Small InterferingSquamous Cell Carcinoma of Head and NeckXenograft Model Antitumor AssaysAnaplastic Lymphoma KinaseAntineoplastic AgentsErbB ReceptorsProtein Kinase InhibitorsRNA, Small InterferingALKEGFREGFR inhibitor resistanceHNSCCpatient-derived models

Identifiers

PMID29856687
PMCPMC6300392
OpenAlexW2806193092

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.