Evidence map›Paper›PMID 32600451›Full record

ArticleClinical epigenetics2020

Identifying epigenetic biomarkers of established prognostic factors and survival in a clinical cohort of individuals with oropharyngeal cancer.

Ryan Langdon, Rebecca Richmond, Hannah R Elliott, Tom Dudding, Nabila Kazmi, Chris Penfold, Kate Ingarfield, Karen Ho, Andrew Bretherick, Chris Haley and 10 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Review
  7. 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

20 authors at 6 institutions in 3 countries.

Ryan LangdonMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK. ryan.langdon@bristol.ac.uk.ORCID 0000-0003-3543-6480
Rebecca RichmondMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK. rebecca.richmond@bristol.ac.uk.
Hannah R ElliottMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Tom DuddingMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Nabila KazmiMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Chris PenfoldNIHR Bristol Biomedical Research Centre, University Hospitals Bristol and University of Bristol, Bristol, UK.
Kate IngarfieldNIHR Bristol Biomedical Research Centre, University Hospitals Bristol and University of Bristol, Bristol, UK.
Karen HoMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Andrew BretherickMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Scotland, Bristol, EH4 2XU, UK.
Chris HaleyMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Scotland, Bristol, EH4 2XU, UK.
Yanni ZengMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Scotland, Bristol, EH4 2XU, UK.
Rosie M WalkerMedical Genetics Section, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Michael PawlitaInfections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Tim WaterboerInfections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Tom GauntMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
George Davey SmithMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Matthew SudermanMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Steve ThomasNIHR Bristol Biomedical Research Centre, University Hospitals Bristol and University of Bristol, Bristol, UK.
Andy NessNIHR Bristol Biomedical Research Centre, University Hospitals Bristol and University of Bristol, Bristol, UK.
Caroline ReltonMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
University of Bristol · GBGerman Cancer Research Center · DEWestern General Hospital · GBAt Bristol · GBInstitute of Genetics and Cancer · GBSun Yat-sen University · CN

Funding

Biotechnology and Biological Sciences Research CouncilCancer Research UK 19169Cancer Research UK C18281/A19169Cancer Research UK C18281/A20988Chief Scientist Office CZD/16/6Department of Health RP-PG-0707-10034Medical Research Council G0700704Medical Research Council MC_PC_U127592696Medical Research Council MC_UU_00007/10Medical Research Council MC_UU_00011/4Medical Research Council MC_UU_00011/5Medical Research Council MR/K026992/1Wellcome TrustWellcome Trust 104036/Z/14/ZWellcome Trust 201268/Z/16/ZWellcome Trust 204979/Z/16/Z
6 · The paper itself

Abstract

backgroundSmoking status, alcohol consumption and HPV infection (acquired through sexual activity) are the predominant risk factors for oropharyngeal cancer and are thought to alter the prognosis of the disease. Here, we conducted single-site and differentially methylated region (DMR) epigenome-wide association studies (EWAS) of these factors, in addition to ∼ 3-year survival, using Illumina Methylation EPIC DNA methylation profiles from whole blood in 409 individuals as part of the Head and Neck 5000 (HN5000) study. Overlapping sites between each factor and survival were then assessed using two-step Mendelian randomization to assess whether methylation at these positions causally affected survival.

resultsUsing the MethylationEPIC array in an OPC dataset, we found novel CpG associations with smoking, alcohol consumption and ~ 3-year survival. We found no CpG associations below our multiple testing threshold associated with HPV16 E6 serological response (used as a proxy for HPV infection). CpG site associations below our multiple-testing threshold (P

conclusionsPart of the effect of smoking on survival in those with oropharyngeal cancer may be mediated by methylation at the SPEG gene locus. Replication in data from independent datasets and data from HN5000 with longer follow-up times is needed to confirm these findings.

Indexed as

AdultAlcohol DrinkingBiomarkersCase-Control StudiesCohort StudiesCpG IslandsDNA MethylationEpigenesis, GeneticEpigenomeEpigenomicsFemaleHumansMaleMendelian Randomization AnalysisMiddle AgedMuscle ProteinsBiomarkersE6 protein, Human papillomavirus type 16KHDC3L protein, humanMuscle ProteinsOncogene Proteins, ViralProteinsProtein Serine-Threonine KinasesRepressor ProteinsSPEG protein, human

Identifiers

PMID32600451
PMCPMC7322918
OpenAlexW3037742494

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.