Evidence map›Paper›PMID 33495197›Full record

ArticleCancer discovery2021

TNIK Is a Therapeutic Target in Lung Squamous Cell Carcinoma and Regulates FAK Activation through Merlin.

Pedro Torres-Ayuso, Elvira An, Katherine M Nyswaner, Ryan C Bensen, Daniel A Ritt, Suzanne I Specht, Sudipto Das, Thorkell Andresson, Raul E Cachau, Roger J Liang and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 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
3.1field-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.

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, 56 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Impact of Targeting TRAF2 and NCK-Interacting Protein Kinase on Antitumor Effect and Tumor Immune Environment in c-MYC-High SCLC.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. TRAF2 and NCK interacting kinase: a novel regulator of integrin αResearch and practice in thrombosis and haemostasis · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. TNIK in disease: from molecular insights to therapeutic prospects.Apoptosis : an international journal on programmed cell death · 2024
    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

20 authors at 4 institutions in 1 country.

Pedro Torres-AyusoLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland. john.brognard@nih.gov torresayusop2@nih.gov.ORCID 0000-0003-2213-9014
Elvira AnLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
Katherine M NyswanerLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
Ryan C BensenLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
Daniel A RittLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
Suzanne I SpechtLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
Sudipto DasProtein Characterization Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Thorkell AndressonProtein Characterization Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Raul E CachauAdvanced Biomedical Computational Science, Biomedical Informatics and Data Science, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Roger J LiangLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
Amy L RiesLaboratory Animal Sciences Program, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Christina M RobinsonLaboratory Animal Sciences Program, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Simone DifilippantonioLaboratory Animal Sciences Program, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Brad GoukerMolecular Histopathology Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Laura BasselMolecular Histopathology Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Baktiar O KarimMolecular Histopathology Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Chad J MillerDepartment of Pharmacology, Yale School of Medicine, New Haven, Connecticut.ORCID 0000-0002-2087-6566
Benjamin E TurkDepartment of Pharmacology, Yale School of Medicine, New Haven, Connecticut.ORCID 0000-0001-9275-4069
Deborah K MorrisonLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland.
John BrognardLaboratory of Cell and Developmental Signaling, Center for Cancer Research, NCI, Frederick, Maryland. john.brognard@nih.gov torresayusop2@nih.gov.
Center for Cancer Research · USLeidos (United States) · USYale University · USFrederick National Laboratory for Cancer Research · US

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
Oncogenic Kinases in CancerZIABC011691 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BROGNARD, JOHN · 2016 to 2025
$14.4M
Role of Protein Scaffolds in RTKRas-dependent Signal TransductionZIABC011107 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MORRISON, DEBORAH · 2009 to 2025
$7.3M
Structure-directed investigations into the regulation of Ste20 kinasesR01GM102262 · NIGMS · YALE UNIVERSITY · PI BOGGON, TITUS JONATHON · 2012 to 2025
$4.2M
Intramural NIH HHS ZIA BC011691NCI NIH HHS 75N91019D00024NIGMS NIH HHS R01 GM102262
6 · The paper itself

Abstract

Lung squamous cell carcinoma (LSCC) is the second most prevalent type of lung cancer. Despite extensive genomic characterization, no targeted therapies are approved for the treatment of LSCC. Distal amplification of the 3q chromosome is the most frequent genomic alteration in LSCC, and there is an urgent need to identify efficacious druggable targets within this amplicon. We identify the protein kinase TNIK as a therapeutic target in LSCC.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Squamous CellCell Line, TumorEpithelial CellsGene Expression Regulation, NeoplasticHumansLung NeoplasmsMiceMolecular Targeted TherapyProtein Kinase InhibitorsProtein Serine-Threonine KinasesAntineoplastic AgentsProtein Kinase InhibitorsProtein Serine-Threonine KinasesTNIK protein, human

Identifiers

PMID33495197
PMCPMC8178189
OpenAlexW3121865115

What OpenQuestion holds

Textmetadata
LicenceTDM
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.