Evidence map›Paper›PMID 35042463›Full record

ArticleBMC genomics2022

Ferroptosis-associated DNA methylation signature predicts overall survival in patients with head and neck squamous cell carcinoma.

Yuanyuan Xu, Min Hong, Deyu Kong, Jun Deng, Zhaoming Zhong, Jin Liang

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
  5. The Role of Methylation in Ferroptosis.Journal of cardiovascular translational research · 2024
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  11. Regulation of Ferroptosis in Lung Adenocarcinoma.International journal of molecular sciences · 2023
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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

6 authors at 3 institutions in 1 country.

Yuanyuan XuDepartment of Oncology, First People's Hospital of Kunming, Kunming, 650000, China.
Min HongDepartment of Medical Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, 650000, China.
Deyu KongDepartment of Medical Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, 650000, China.
Jun DengDepartment of Medical Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, 650000, China.
Zhaoming ZhongDepartment of Medical Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, 650000, China. zhongzhm@ydyy.cn.
Jin LiangDepartment of Medical Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, 650000, China. liangjin@kmmu.edu.cn.
Kunming Medical University · CNFirst Affiliated Hospital of Kunming Medical University · CNThe First Hospital of Kunming · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHead and neck squamous cell carcinoma (HNSCC) is a common cancer characterized by late diagnosis and poor prognosis. The aim of this study was to identify a novel ferroptosis-related DNA methylation signature as an alternative diagnosis index for patients with HNSCC.

methodsMethylome and transcriptome data of 499 HNSCC patients, including 275 oral squamous cell carcinoma (OSCC) samples, were obtained from The Cancer Genome Atlas (TCGA). An additional independent methylation dataset of 50 OSCC patients from the NCBI Gene Expression Omnibus (GEO) database was used for validation. As an index of ferroptosis activity, the ferroptosis score (FS) of each patient was inferred from the transcriptome data using single-sample gene set enrichment analysis. Univariate, multivariate, and LASSO Cox regression analyses were used to select CpG sites for the construction of a ferroptosis-related DNA methylation signature for diagnosis of patients.

resultsWe initially inferred the FS of each TCGA HNSCC patient and divided the samples into high- and low-FS subgroups. Results showed that the high-FS subgroup displayed poor overall survival. Moreover, 378 differentially methylated CpG sites (DMCs) were identified between the two HNSCC subgroups, with 16 selected to construct a 16-DNA methylation signature for risk prediction in HNSCC patients using the LASSO and multivariate Cox regression models. Relative operating characteristic (ROC) curve analysis showed great predictive efficiency for 1-, 3-, and 5-year HNSCC survival using the 16-DNA methylation signature. Its predictive efficiency was also observed in OSCC patients from the TCGA and GEO databases. In addition, we found that the signature was associated with the fractions of immune types in the tumor immune microenvironment (TIME), suggesting potential interactions between ferroptosis and TIME in HNSCC progression.

conclusionsWe established a novel ferroptosis-related 16-DNA methylation signature that could be applied as an alternative tool to predict prognosis outcome in patients with HNSCC, including OSCC.

Indexed as

Carcinoma, Squamous CellFerroptosisHead and Neck NeoplasmsMouth NeoplasmsDNA MethylationGene Expression Regulation, NeoplasticHumansPrognosisSquamous Cell Carcinoma of Head and NeckTumor MicroenvironmentDiagnostic indicatorDNA methylation signatureFerroptosisHead and neck squamous cell carcinomaOral squamous cell carcinoma

Identifiers

PMID35042463
PMCPMC8767683
OpenAlexW4205201399

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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.