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Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
Comprehensive analysis reveals common DNA methylation patterns of tobacco-associated cancers: A pan-cancer analysis
Xingyu Liu1, Jiarui Chen1, Jiali Li1
1Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Abstract:
The role of tobacco in carcinogenesis has received increasing attention across a number of disciplines in recent years. Accumulating evidences reveal that tobacco consumption affects various epigenetic modifications, especially DNA methylation. However, the genetic modifications of methylation patterns involved in tobacco-attributable cancers remain poorly understood. In this manuscript, aberrant DNA methylation patterns were investigated in 9 tobacco-attributable cancers. Differential methylated probes (DMPs) were identified in each cancer type and a total of 2,392 hyper- and 736 hypomethylated pan-cancer DMPs (PDMPs) were screened out for further analysis. PDMP-associated genes were mostly enriched in metabolism-associated pathways, suggesting the potential roles of methylation alternation in reprogramming cancer cell metabolism. Hypomethylated PDMPs cg12422154, cg02772121 and cg06051311 constituted an enhancer region, significantly downregulating TRIM15, TRIM26 and RPP21, which serve as epigenetically therapeutic biomarkers. Forty-three hypermethylated and 13 hypomethylated transcription factor motifs were clustered into 6 groups, and exhibited various biological functions. Forty-nine PDMPs were reported to be associated with prognosis, providing effective tools to predict clinical outcomes. In summary, our studies revealed the characteristics, influences and potential mechanisms of DNA methylation patterns of tobacco-attributable cancer.
Insights
Tobacco use significantly alters DNA methylation patterns in nine cancers, impacting cellular metabolism and offering potential therapeutic biomarkers and prognostic tools for tobacco-attributable cancers.
Area of Science:
- Epigenetics
- Oncology
- Molecular Biology
Background:
- Tobacco consumption is a major cause of cancer.
- Epigenetic modifications, particularly DNA methylation, are implicated in tobacco-related carcinogenesis.
- Understanding methylation patterns in tobacco-attributable cancers is crucial.
Purpose of the Study:
- To investigate aberrant DNA methylation patterns in nine tobacco-attributable cancers.
- To identify pan-cancer differentially methylated probes (PDMPs) and associated genes.
- To explore the functional and prognostic implications of these methylation patterns.
Main Methods:
- Analysis of DNA methylation data across nine cancer types.
- Identification of differentially methylated probes (DMPs) and pan-cancer DMPs (PDMPs).
- Gene enrichment analysis and investigation of specific methylation sites and transcription factor motifs.
Main Results:
- Identified 2,392 hyper- and 736 hypomethylated PDMPs.
- PDMP-associated genes were enriched in metabolism-related pathways.
- Discovered specific hypomethylated probes regulating TRIM15, TRIM26, and RPP21, and identified 49 PDMPs associated with prognosis.
Conclusions:
- Tobacco-attributable cancers exhibit distinct DNA methylation characteristics.
- Aberrant DNA methylation influences cancer cell metabolism and provides potential therapeutic targets.
- PDMPs can serve as biomarkers for prognosis and therapeutic intervention in tobacco-related cancers.
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