Evidence map›Paper›PMID 32986729›Full record

ArticlePloS one2020

Signatures of somatic mutations and gene expression from p16INK4A positive head and neck squamous cell carcinomas (HNSCC).

Nabil F Saba, Ashok R Dinasarapu, Kelly R Magliocca, Bhakti Dwivedi, Sandra Seby, Zhaohui S Qin, Mihir Patel, Christopher C Griffith, Xu Wang, Mark El-Deiry and 5 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 25% 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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 1 country.

Nabil F SabaWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.ORCID 0000-0003-4972-1477
Ashok R DinasarapuDepartment of Human Genetics, Emory University, Atlanta, GA, United States of America.
Kelly R MaglioccaWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Bhakti DwivediWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Sandra SebyCenters for Disease Control (CDC), Atlanta, GA, United States of America.
Zhaohui S QinDepartment of Biostatistics and Bioinformatics, Emory University Atlanta, Atlanta, GA, United States of America.
Mihir PatelWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Christopher C GriffithDepartment of Pathology, Cleveland Clinics, Cleveland, OH, United States of America.
Xu WangWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Mark El-DeiryWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Conor Ernst SteuerWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Jeanne KowalskiDepartment of Oncology, Dell Medical School, Austin, Texas, United States of America.
Dong Moon ShinWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Michael E ZwickDepartment of Human Genetics, Emory University, Atlanta, GA, United States of America.
Zhuo Georgia ChenWinship Cancer Institute, Emory University, Atlanta, GA, United States of America.
Emory University · USCenters for Disease Control and Prevention · USCleveland Clinic · USDell Children's Medical Center of Central Texas · US

Funding

A Novel genomics-based approach to differentiate HPV-positive and -negative HNCR21CA182661 · NCI · EMORY UNIVERSITY · PI CHEN, ZHUO GEORGIA, SABA, NABIL F · 2014 to 2015
$373k
NCI NIH HHS R21 CA182661
6 · The paper itself

Abstract

Human papilloma virus (HPV) causes a subset of head and neck squamous cell carcinomas (HNSCC) of the oropharynx. We combined targeted DNA- and genome-wide RNA-sequencing to identify genetic variants and gene expression signatures respectively from patients with HNSCC including oropharyngeal squamous cell carcinomas (OPSCC). DNA and RNA were purified from 35- formalin fixed and paraffin embedded (FFPE) HNSCC tumor samples. Immuno-histochemical evaluation of tumors was performed to determine the expression levels of p16INK4A and classified tumor samples either p16+ or p16-. Using ClearSeq Comprehensive Cancer panel, we examined the distribution of somatic mutations. Somatic single-nucleotide variants (SNV) were called using GATK-Mutect2 ("tumor-only" mode) approach. Using RNA-seq, we identified a catalog of 1,044 and 8 genes as significantly expressed between p16+ and p16-, respectively at FDR 0.05 (5%) and 0.1 (10%). The clinicopathological characteristics of the patients including anatomical site, smoking and survival were analyzed when comparing p16+ and p16- tumors. The majority of tumors (65%) were p16+. Population sequence variant databases, including gnomAD, ExAC, COSMIC and dbSNP, were used to identify the mutational landscape of somatic sequence variants within sequenced genes. Hierarchical clustering of The Cancer Genome Atlas (TCGA) samples based on HPV-status was observed using differentially expressed genes. Using RNA-seq in parallel with targeted DNA-seq, we identified mutational and gene expression signatures characteristic of p16+ and p16- HNSCC. Our gene signatures are consistent with previously published data including TCGA and support the need to further explore the biologic relevance of these alterations in HNSCC.

Indexed as

AdultAgedCyclin-Dependent Kinase Inhibitor p16Databases, Nucleic AcidData ManagementDiagnostic Tests, RoutineDNA, ViralFemaleGene ExpressionGene Expression ProfilingHead and Neck NeoplasmsHumansMaleMiddle AgedMutationOropharyngeal NeoplasmsCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16DNA, Viral

Identifiers

PMID32986729
PMCPMC7521680
OpenAlexW3089701442

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.