Evidence map›Paper›PMID 23451093›Full record

ArticlePloS one2013

Molecular subtypes in head and neck cancer exhibit distinct patterns of chromosomal gain and loss of canonical cancer genes.

Vonn Walter, Xiaoying Yin, Matthew D Wilkerson, Christopher R Cabanski, Ni Zhao, Ying Du, Mei Kim Ang, Michele C Hayward, Ashley H Salazar, Katherine A Hoadley and 15 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 193 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
193citing papers in PubMed, 2 pooled it
41.1field-weighted citation impact, top 1% 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

193 citing papers in PubMed, 2 syntheses or guidelines pooled it, 335 citations in OpenAlex.

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  8. Multivariate Random Forests for Cross-Modal Multi-Omics Integration.bioRxiv : the preprint server for biology · 2026
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133 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 5 institutions in 2 countries.

Vonn WalterLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Xiaoying Yin
Matthew D Wilkerson
Christopher R Cabanski
Ni Zhao
Ying Du
Mei Kim Ang
Michele C Hayward
Ashley H Salazar
Katherine A Hoadley
Karen Fritchie
Charles J Sailey
Charles G Sailey
Mark C Weissler
William W Shockley
Adam M Zanation
Trevor Hackman
Leigh B Thorne
William D Funkhouser
Kenneth L Muldrew
Andrew F Olshan
Scott H Randell
Fred A Wright
Carol G Shores
D Neil Hayes
University of North Carolina at Chapel Hill · USNational Cancer Centre Singapore · SGUniversity of Arkansas for Medical Sciences · USUniversity of Toledo · USWinnMed · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
Multidisciplinary Clinical Research Career Develop(RMI)K12RR023248 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ORRINGER, EUGENE P · 2005 to 2007
$6.3M
Space-time Modeling for Linking Climate Change,Pollutant Exposure, Built EnvironmR01ES014843 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI REICH, BRIAN J. · 2008 to 2013
$2.0M
NCI NIH HHS P30 CA016086NCRR NIH HHS K12 RR023248NCRR NIH HHS K12-RR-023248NIEHS NIH HHS P30 ES010126NIEHS NIH HHS R01 ES014843
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a frequently fatal heterogeneous disease. Beyond the role of human papilloma virus (HPV), no validated molecular characterization of the disease has been established. Using an integrated genomic analysis and validation methodology we confirm four molecular classes of HNSCC (basal, mesenchymal, atypical, and classical) consistent with signatures established for squamous carcinoma of the lung, including deregulation of the KEAP1/NFE2L2 oxidative stress pathway, differential utilization of the lineage markers SOX2 and TP63, and preference for the oncogenes PIK3CA and EGFR. For potential clinical use the signatures are complimentary to classification by HPV infection status as well as the putative high risk marker CCND1 copy number gain. A molecular etiology for the subtypes is suggested by statistically significant chromosomal gains and losses and differential cell of origin expression patterns. Model systems representative of each of the four subtypes are also presented.

Indexed as

AgedCarcinoma, Squamous CellChromosome AberrationsClass I Phosphatidylinositol 3-KinasesCyclin D1DNA Copy Number VariationsErbB ReceptorsFemaleHead and Neck NeoplasmsHumansIntracellular Signaling Peptides and ProteinsKelch-Like ECH-Associated Protein 1MaleMiddle AgedNF-E2-Related Factor 2Phosphatidylinositol 3-KinasesCCND1 protein, humanClass I Phosphatidylinositol 3-KinasesCyclin D1EGFR protein, humanErbB ReceptorsIntracellular Signaling Peptides and ProteinsKEAP1 protein, humanKelch-Like ECH-Associated Protein 1NFE2L2 protein, humanNF-E2-Related Factor 2Phosphatidylinositol 3-KinasesPIK3CA protein, humanSOX2 protein, humanSOXB1 Transcription FactorsTP63 protein, humanTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID23451093
PMCPMC3579892
OpenAlexW2076419931

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.