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Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
Relationships between MGMT promoter methylation and gastric cancer: a meta-analysis
1Department of Laboratory Medicine, Center for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Abstract:
A DNA repair enzyme, O6-methylguanine-DNA methyltransferase (MGMT), plays an important role in the development of gastric cancers. However, the role of MGMT promoter methylation in the occurrence of gastric cancer and its relationships with clinicopathologic characteristics has not been fully clarified. Thus, we performed a meta-analysis to evaluate the associations between MGMT promoter methylation and gastric cancer. Electronic databases, including PubMed and Web of Science, were used to systematically search related clinical studies published in English until April 1, 2016. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated to evaluate the associations between MGMT promoter methylation and gastric cancer risk or clinicopathologic characteristics. A total of 16 studies including 1,935 patients and 1,948 control persons were included in the analysis. Our study suggested that MGMT promoter methylation frequency was associated with gastric cancer (OR=3.46, 95% CI: 2.13-5.61, P<0.001). Moreover, the frequency of MGMT promoter methylation in the no lymph node metastasis group was lower than that in lymph node metastasis group, with marginal significance (OR=0.65, 95% CI: 0.42-1.01, P=0.05). Additionally, the methylation rate of the MGMT promoter was much lower in patients without distant metastases than in those with metastases (OR=0.27, 95% CI: 0.18-0.40, P<0.001). No significant association of MGMT promoter methylation with Lauren classification, tumor location, tumor invasion, or Helicobacter pylori infection was found. In conclusion, the methylation status of the MGMT promoter was related to gastric cancer risk, distant metastasis, and lymph node metastasis, which indicates that MGMT promoter methylation may play an important role in gastric cancer development.
Insights
O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation is linked to increased gastric cancer risk and metastasis. This finding highlights MGMT
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- O6-methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme crucial in gastric cancer development.
- The specific role of MGMT promoter methylation in gastric cancer occurrence and its association with clinical features remain unclear.
Purpose of the Study:
- To conduct a meta-analysis evaluating the association between MGMT promoter methylation and gastric cancer.
- To investigate the relationship between MGMT promoter methylation and various clinicopathologic characteristics of gastric cancer.
Main Methods:
- Systematic literature search of PubMed and Web of Science for studies published up to April 1, 2016.
- Inclusion of 16 studies comprising 1,935 gastric cancer patients and 1,948 controls.
- Calculation of Odds Ratios (ORs) and 95% Confidence Intervals (CIs) to assess associations.
Main Results:
- MGMT promoter methylation was significantly associated with an increased risk of gastric cancer (OR=3.46, P<0.001).
- Lower MGMT promoter methylation frequency was observed in patients without lymph node metastasis (OR=0.65, P=0.05).
- Significantly lower MGMT promoter methylation rates were found in patients without distant metastases compared to those with metastases (OR=0.27, P<0.001).
- No significant associations were found with Lauren classification, tumor location, invasion, or Helicobacter pylori infection.
Conclusions:
- MGMT promoter methylation is a significant risk factor for gastric cancer.
- MGMT promoter methylation status correlates with lymph node and distant metastasis in gastric cancer patients.
- These findings suggest MGMT promoter methylation plays a critical role in gastric cancer progression.
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