Evidence map›Paper›PMID 27935865›Full record

ArticleOncotarget2017

Bronchial airway gene expression signatures in mouse lung squamous cell carcinoma and their modulation by cancer chemopreventive agents.

Donghai Xiong, Jing Pan, Qi Zhang, Eva Szabo, Mark Steven Miller, Ronald A Lubet, Ming You, Yian Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Study on the Mechanism of Competing Endogenous Network of 'Current computer-aided drug design · 2025
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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

8 authors at 2 institutions in 1 country.

Donghai XiongCancer Center, Medical College of Wisconsin, WI 53226, USA.
Jing PanCancer Center, Medical College of Wisconsin, WI 53226, USA.
Qi ZhangCancer Center, Medical College of Wisconsin, WI 53226, USA.
Eva SzaboChemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Rockville, MD 20850, USA.
Mark Steven MillerChemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Rockville, MD 20850, USA.
Ronald A LubetChemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Rockville, MD 20850, USA.
Ming YouCancer Center, Medical College of Wisconsin, WI 53226, USA.
Yian WangCancer Center, Medical College of Wisconsin, WI 53226, USA.
Medical College of Wisconsin · USNational Cancer Institute · US

Funding

Chemoprevention of Lung Cancer with Mitochondria-Targeted HonokiolR01CA208648 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KALYANARAMAN, BALARAMAN, YOU, MING · 2017 to 2021
$3.1M
Genome-Wide Association Studies of Inherited Predisposition to Lung CancerR01CA134682 · NCI · WASHINGTON UNIVERSITY · PI LIU, PENGYUAN, YOU, MING · 2009 to 2013
$2.2M
MOLECULAR GENETICS OF LUNG TUMOR PROMOTION IN MICER01CA134433 · NCI · WASHINGTON UNIVERSITY · PI LIU, PENGYUAN, VIKIS, HARIS G. · 2009 to 2013
$1.5M
NCI NIH HHS R01 CA134433NCI NIH HHS R01 CA134682NCI NIH HHS R01 CA208648
6 · The paper itself

Abstract

Due to exposure to environmental toxicants, a "field cancerization" effect occurs in the lung resulting in the development of a field of initiated but morphologically normal appearing cells in the damaged epithelium of bronchial airways with dysregulated gene expression patterns. Using a mouse model of lung squamous cell carcinoma (SCC), we performed transcriptome sequencing (RNA-Seq) to profile bronchial airway gene expression and found activation of the PI3K and Myc signaling networks in cytologically normal bronchial airway epithelial cells of mice with preneopastic lung SCC lesions, which was reversed by treatment with the PI3K Inhibitor XL-147 and pioglitazone, respectively. Activated MYC signaling was also present in premalignant and tumor tissues from human lung SCC patients. In addition, we identified a key microRNA, mmu-miR-449c-5p, whose suppression significantly up-regulated Myc expression in the normal bronchial airway epithelial cells of mice with early stage SCC lesions. We developed a novel bronchial genomic classifier in mice and validated it in humans. In the classifier, Ppbp (pro-platelet basic protein) was overexpressed 115 fold in the bronchial airways of mice with preneoplastic lung SCC lesions. This is the first report that demonstrates Ppbp as a novel biomarker in the bronchial airway for lung cancer diagnosis.

Indexed as

AnimalsBiomarkers, TumorBronchiCarcinoma, Squamous CellChemokines, CXCChemopreventionDisease Models, AnimalGene Expression ProfilingLung NeoplasmsMicePioglitazonePrecancerous ConditionsQuinoxalinesSulfonamidesThiazolidinedionesTranscriptomeBiomarkers, TumorChemokines, CXCCxcl7 protein, mousePioglitazoneQuinoxalinesSulfonamidesThiazolidinedionesXL147AUC (area under the curve)GSEA (gene set enrichment analysis)IPA (Ingenuity Pathway Analysis)PPAR (peroxisome proliferator-activated receptor gamma)SCC (squamous cell carcinoma)

Identifiers

PMID27935865
PMCPMC5386655
OpenAlexW2560258182

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.