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Updated: Aug 7, 2026

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
Aberrant methylation of the CHFR gene in digestive tract cancer
Yuki Morioka1, Kenji Hibi, Mitsuru Sakai
1Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya 466-8560, Japan.
Background:
Recently, aberrant methylation of the CHFR gene associated with gene silencing has been reported in several cancers. The methylation status of the CHFR gene was examined in primary esophageal and gastric carcinomas.
Materials And Methods:
The methylation status of the CHFR promoter region and mRNA expression in cancer cell lines were examined first. The methylation status of the CHFR gene in 38 esophageal and 53 gastric cancers was subsequently examined and the correlation between CHFR methylation and the clinicopathological findings was investigated.
Results:
Aberrant methylation of the CHFR gene was detected in 9 out of 38 (24%) primary esophageal and 16 out of 53 (30%) primary gastric cancers. After methylation analysis of all the samples, the clinicopathological data were correlated with these results. There was a significant difference according to gender (p = 0.0404), indicating that female esophageal cancers were more frequently methylated than male. On the other hand, abnormal methylation was found in esophageal and gastric cancer patients at all clinical stages.
Conclusion:
Aberrant methylation of the CHFR gene was frequently shown in esophageal and gastric cancers. In addition, abnormal methylation was found in these cancer patients at all clinical stages, suggesting that this cancer could be methylated at an early stage.
Insights
Aberrant methylation of the CHFR gene is common in esophageal and gastric cancers. This gene methylation occurs across all clinical stages, suggesting it may be an early event in cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Aberrant methylation of the CHFR gene is linked to gene silencing in various cancers.
- The CHFR gene's methylation status was investigated in esophageal and gastric carcinomas.
Purpose of the Study:
- To examine the methylation status of the CHFR gene in primary esophageal and gastric cancers.
- To correlate CHFR gene methylation with clinicopathological findings.
Main Methods:
- CHFR promoter methylation and mRNA expression analyzed in cancer cell lines.
- CHFR gene methylation assessed in 38 esophageal and 53 gastric cancer samples.
- Correlation analysis between CHFR methylation and clinicopathological data performed.
Main Results:
- CHFR gene aberrant methylation detected in 24% of esophageal and 30% of gastric cancers.
- Female esophageal cancers showed significantly higher methylation rates than male cancers (p = 0.0404).
- Abnormal CHFR methylation was observed across all clinical stages for both cancer types.
Conclusions:
- Frequent aberrant methylation of the CHFR gene observed in esophageal and gastric cancers.
- CHFR gene methylation occurs at all clinical stages, indicating potential early-stage involvement.
- CHFR methylation may serve as an early biomarker for esophageal and gastric cancers.
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