Related Experiment Video
Updated: Nov 30, 2025

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Aberrant DNA Methylation in Esophageal Squamous Cell Carcinoma: Biological and Clinical Implications
Lehang Lin1, Xu Cheng1, Dong Yin1
1Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Medical Research Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Abstract:
Almost all cancer cells possess multiple epigenetic abnormalities, which cooperate with genetic alterations to enable the acquisition of cancer hallmarks during tumorigenesis. As the most frequently found epigenetic change in human cancers, aberrant DNA methylation manifests at two major forms: global genomic DNA hypomethylation and locus-specific promoter region hypermethylation. It has been recognized as a critical contributor to esophageal squamous cell carcinoma (ESCC) malignant transformation. In ESCC, DNA methylation alterations affect genes involved in cell cycle regulation, DNA damage repair, and cancer-related signaling pathways. Aberrant DNA methylation patterns occur not only in ESCC tumors but also in precursor lesions. It adds another layer of complexity to the ESCC heterogeneity and may serve as early diagnostic, prognostic, and chemo-sensitive markers. Characterization of the DNA methylome in ESCC could help better understand its pathogenesis and develop improved therapies. We herein summarize the current research and knowledge about DNA methylation in ESCC and its clinical significance in diagnosis, prognosis, and treatment.
Insights
Aberrant DNA methylation is a key epigenetic change in esophageal squamous cell carcinoma (ESCC). Understanding these DNA methylation patterns is crucial for developing new diagnostic and therapeutic strategies for ESCC.
Area of Science:
- Epigenetics and Cancer Biology
- Molecular Oncology
- Genomic Medicine
Background:
- Epigenetic abnormalities, particularly aberrant DNA methylation, are hallmarks of cancer, cooperating with genetic alterations.
- Aberrant DNA methylation in esophageal squamous cell carcinoma (ESCC) includes global hypomethylation and locus-specific hypermethylation.
- These alterations impact genes critical for cell cycle regulation, DNA repair, and cancer signaling pathways in ESCC.
Purpose of the Study:
- To summarize current knowledge on DNA methylation in ESCC.
- To explore the clinical significance of DNA methylation in ESCC diagnosis, prognosis, and treatment.
- To highlight the role of DNA methylation in ESCC pathogenesis and heterogeneity.
Main Methods:
- Review of existing research on DNA methylation patterns in ESCC.
- Analysis of the impact of DNA methylation on gene expression and function in ESCC.
- Evaluation of DNA methylation as potential biomarkers for ESCC.
Main Results:
- Aberrant DNA methylation is prevalent in ESCC, affecting key cancer-related genes.
- Altered methylation patterns are observed in both ESCC tumors and precursor lesions.
- DNA methylation alterations contribute to ESCC heterogeneity and may serve as diagnostic and prognostic markers.
Conclusions:
- DNA methylation is a critical factor in ESCC development and progression.
- Characterizing the ESCC methylome offers insights into pathogenesis and potential therapeutic targets.
- Aberrant DNA methylation holds promise as biomarkers for early diagnosis, prognosis, and predicting chemosensitivity in ESCC.
Related Concept Videos
Epigenetic Regulation
X-chromosome...
Epigenetic Regulation
Barrett Esophagus-I: Introduction
This constant acid exposure transforms the esophagus's pink mucosal lining (stratified squamous epithelium) into a type of lining more...
Barrett Esophagus-II: Clinical Manifestations and Management
To diagnose Barrett's esophagus, healthcare providers often recommend an endoscopy for those showing symptoms of acid reflux. The procedure...
Abnormal Proliferation

