Evidence map›Paper›PMID 26917230›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2016

A Sensitive NanoString-Based Assay to Score STK11 (LKB1) Pathway Disruption in Lung Adenocarcinoma.

Lu Chen, Brienne E Engel, Eric A Welsh, Sean J Yoder, Stephen G Brantley, Dung-Tsa Chen, Amer A Beg, Chunxia Cao, Frederic J Kaye, Eric B Haura and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Comprehensively Testing the Function of Missense Variation in thebioRxiv : the preprint server for biology · 2025
    Article
  4. LKB1 biology: assessing the therapeutic relevancy of LKB1 inhibitors.Cell communication and signaling : CCS · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. BeyondPharmaceuticals (Basel, Switzerland) · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Somatic Mutations and Ancestry Markers in Hispanic Lung Cancer Patients.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2017
    Article
  19. Article
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 3 institutions in 1 country.

Lu ChenDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida; Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Brienne E EngelDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Eric A WelshDepartment of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Sean J YoderMolecular Genomics Core, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Stephen G BrantleyPathology Services M2Gen, Tampa, Florida.
Dung-Tsa ChenDepartment of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Amer A BegDepartment of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Chunxia CaoDepartment of Medicine, University of Florida, Gainesville, Florida.
Frederic J KayeDepartment of Medicine, University of Florida, Gainesville, Florida.
Eric B HauraDepartment of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Matthew B SchabathDepartment of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
W Douglas CressDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida. Electronic address: Douglas.Cress@moffitt.org.
Moffitt Cancer Center · USMolecular Oncology (United States) · USUniversity of Florida · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI John L. Cleveland · 1998 to 2026
$93.5M
SPORE in Lung CancerP50CA119997 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI HAURA, ERIC B. · 2008 to 2012
$11.0M
Transcriptional Control of Mcl-1 and Bok/Mtd by E2F1R01CA090489 · NCI · H. LEE MOFFITT CANCER CTR &RES INST · PI CRESS, WILLIAM D · 2003 to 2007
$1.6M
Partnership--Moffitt Cancer--Puerto Rico Cancer CenterP20CA091353 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI PLEDGER, WARREN JACKSON · 2001 to 2004
$690k
NCI NIH HHS P20 CA091353NCI NIH HHS P30 CA076292NCI NIH HHS P50 CA119997NCI NIH HHS R01 CA090489
6 · The paper itself

Abstract

introductionSerine/threonine kinase 11 gene (STK11), better known as liver kinase β1, is a tumor suppressor that is commonly mutated in lung adenocarcinoma (LUAD). Previous work has shown that mutational inactivation of the STK11 pathway may serve as a predictive biomarker for cancer treatments, including phenformin and cyclooxygenase-2 inhibition. Although immunohistochemical (IHC) staining and diagnostic sequencing are used to measure STK11 pathway disruption, there are serious limitations to these methods, thus emphasizing the importance of validating a clinically useful assay.

methodsAn initial STK11 mutation mRNA signature was generated using cell line data and refined using three large, independent patient databases. The signature was validated as a classifier using The Cancer Genome Atlas (TCGA) LUAD cohort as well as a 442-patient LUAD cohort developed at Moffitt. Finally, the signature was adapted to a NanoString-based format and validated using RNA samples isolated from formalin-fixed, paraffin-embedded tissue blocks corresponding to a cohort of 150 patients with LUAD. For comparison, STK11 IHC staining was also performed.

resultsThe STK11 signature was found to correlate with null mutations identified by exon sequencing in multiple cohorts using both microarray and NanoString formats. Although there was a statistically significant correlation between reduced STK11 protein expression by IHC staining and mutation status, the NanoString-based assay showed superior overall performance, with a -0.1588 improvement in area under the curve in receiver-operator characteristic curve analysis (p < 0.012).

conclusionThe described NanoString-based STK11 assay is a sensitive biomarker to study emerging therapeutic modalities in clinical trials.

Indexed as

MutationAdenocarcinomaAMP-Activated Protein Kinase KinasesBiological AssayBiomarkers, TumorCohort StudiesHumansLung NeoplasmsNanotechnologyNeoplasm StagingPrognosisProtein Serine-Threonine KinasesROC CurveAMP-Activated Protein Kinase KinasesBiomarkers, TumorProtein Serine-Threonine KinasesSTK11 protein, humanbiomarkerCOX-2 inhibitionLKB1NanoStringSTK11

Identifiers

PMID26917230
PMCPMC4877210
OpenAlexW2283559404

What OpenQuestion holds

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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.