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Updated: May 26, 2026

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
PDCD4 expression inversely correlated with miR-21 levels in gastric cancers
Zhang Cao1, Jung Hwan Yoon, Suk Woo Nam
1Department of Pathology, College of Medicine, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul 137-701, Korea.
Purpose:
The specific aim of this study was to investigate whether the PDCD4 gene is involved in the development and progression of gastric cancer.
Methods:
We examined the genetic and epigenetic alterations of the PDCD4 gene as well as the expression of PDCD4 protein in gastric cancers. The mRNA expression of PDCD4 and miRNA-21 expression were also analyzed using quantitative real-time RT-PCR.
Results:
Loss or reduced PDCD4 expression was observed in 79 (36.7%) of 215 gastric cancer specimens. Statistically, altered PDCD4 expression was not associated with the clinicopathological parameters, including tumor differentiation, location, lymph node metastasis and overall survival (P > 0.05). miRNA-21 overexpression was frequently detected in gastric cancers (31 of 46, 67.4%), and there was a significant inverse correlation between miRNA-21 and PDCD4 protein expression (P = 0.029), but not between miRNA-21 and PDCD4 mRNA expression. In genetic analysis, no mutation was detected in the coding region of the PDCD4 gene, and promoter hypermethylation was found in 24 (36.4%) of the 66 gastric cancer samples.
Conclusions:
Our data suggest that overexpression of miRNA-21 and reduced or loss of PDCD4 expression may play a role in the development and progression of gastric cancers.
Insights
Reduced Programmed Cell Death 4 (PDCD4) expression and elevated miRNA-21 levels are linked to gastric cancer development and progression. These findings suggest potential roles in the disease
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer remains a significant global health challenge.
- Understanding the molecular mechanisms underlying gastric cancer development is crucial for targeted therapies.
Purpose of the Study:
- To investigate the role of the Programmed Cell Death 4 (PDCD4) gene in gastric cancer.
- To analyze genetic and epigenetic alterations of PDCD4 and its protein expression in gastric tumors.
Main Methods:
- Examined genetic and epigenetic alterations of the PDCD4 gene.
- Assessed PDCD4 protein and mRNA expression via quantitative real-time RT-PCR.
- Analyzed miRNA-21 expression and its correlation with PDCD4.
Main Results:
- Loss or reduced PDCD4 expression occurred in 36.7% of gastric cancers.
- No association found between PDCD4 expression and clinicopathological parameters.
- miRNA-21 overexpression correlated inversely with PDCD4 protein but not mRNA levels.
- Promoter hypermethylation of PDCD4 was detected in 36.4% of samples.
Conclusions:
- Reduced PDCD4 expression and miRNA-21 overexpression may contribute to gastric cancer development.
- These molecular changes present potential therapeutic targets for gastric cancer.
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