2007•Zhongliu fangzhi yanjiuRequires access

Relationship between Hypermethylation of Runx3 Gene in Promoter Region and Cogenesis, Metastasis of Gastric Carcinoma

Yu Liu

Open publisher page 0 citations

Abstract

Objective To investigate the felationship of methylation of human runt-related transcription factor 3 (Runx3) gene on metastasis and oncogenesis of gastric arcinoma. Methods Using RT-PCR technique, specimens from 80 gastric cancer patients (tumor tissues,adjacent tissues) were detected for their expression of the Runx3 gene. Meanwhile, Methylation-specific PCR was used to detect methylation of Runx3 promoter region. Results The expression of Runx3 gene mRNA detected in gastric carcinoma (0.5971±0.1013)was lower than that in adjacent tissues samples(0.8297±0.2912)(t=6.7480, P0.05). No methylation of Runx3 promoter was found in adjacent tissues samples. But it was found in 43 cases in 80 gastric carcinoma specimens. The rate of methylation of Runx3 promoter in gastric carcinoma was higher than that in adjacent tissues(P0.05).The Runx3 mRNA were down-regulated in lymphnode metastasis or poorly differentiated groups, but the Runx3 promoter methylation were detected in those groups markedly. A significant difference was noted between two groups (P0.05). ConclusionHypermethylation was one of reasons which induced Runx3 gene inactivation in human gastric carcinoma. Methylation of Runx3 promoter maybe correlated to on cogenesis, metastasis of gastric carcinoma.

About this research paper

What this paper is about

Objective To investigate the felationship of methylation of human runt-related transcription factor 3 (Runx3) gene on metastasis and oncogenesis of gastric arcinoma. Methods Using RT-PCR technique, specimens from 80 gastric cancer patients (tumor tissues,adjacent tissues) were detected for their expression of the Runx3 gene. Meanwhile, Methylation-specific PCR was used to detect methylation of Runx3 promoter region. Results The expression of Runx3 gene mRNA detected in gastric carcinoma (0.5971±0.1013)was lower than that in adjacent tissues samples(0.8297±0.2912)(t=6.7480, P0.05). No methylation of Runx3 promoter was found in adjacent tissues samples. But it was found in 43 cases in 80 gastric carcinoma specimens. The rate of methylation of Runx3 promoter in gastric carcinoma was higher than that in adjacent tissues(P0.05).The Runx3 mRNA were down-regulated in lymphnode metastasis or poorly differentiated groups, but the Runx3 promoter methylation were detected in those groups markedly. A significant difference was noted between two groups (P0.05). ConclusionHypermethylation was one of reasons which induced Runx3 gene inactivation in human gastric carcinoma. Methylation of Runx3 promoter maybe correlated to on cogenesis, metastasis of gastric carcinoma.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the felationship of methylation of human runt-related transcription factor 3 (Runx3) gene on metastasis and oncogenesis of gastric arcinoma. Methods Using RT-PCR technique, specimens from 80 gastric cancer patients (tumor tissues,adjacent tissues) were detected for their expression of the Runx3 gene. Meanwhile, Methylation-specific PCR was used to detect methylation of Runx3 promoter region. Results The expression of Runx3 gene mRNA detected in gastric carcinoma (0.5971±0.1013)was lower than that in adjacent tissues samples(0.8297±0.2912)(t=6.7480, P0.05). No methylation of Runx3 promoter was found in adjacent tissues samples. But it was found in 43 cases in 80 gastric carcinoma specimens. The rate of methylation of Runx3 promoter in gastric carcinoma was higher than that in adjacent tissues(P0.05).The Runx3 mRNA were down-regulated in lymphnode metastasis or poorly differentiated groups, but the Runx3 promoter methylation were detected in those groups markedly. A significant difference was noted between two groups (P0.05). ConclusionHypermethylation was one of reasons which induced Runx3 gene inactivation in human gastric carcinoma. Methylation of Runx3 promoter maybe correlated to on cogenesis, metastasis of gastric carcinoma.

Key concepts: Methylation, Carcinogenesis, DNA methylation, Metastasis, Promoter, Cancer research, Cancer, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Relationship between Hypermethylation of Runx3 Gene in Promoter Region and Cogenesis, Metastasis of Gastric Carcinoma — Research Paper | ScholarLens