Detection of Promoter Hypermethylation and mRNA Expression of 14-3-3σ Gene in Tissues of Human Hepatocellular Carcinoma
LV Jun
Abstract
LV Jun
Abstract
Objective To investigate promoter methylation status,mRNA expression of 14-3-3σ gene and their relationship in hepatocellular carcinoma(HCC).Methods The methylation status of the 14-3-3σ gene in tissues were detected with methylation-specific PCR.The 14-3-3σ mRNA expression was examined by real-time PCR.Results Hypermethylation of CpG islands of the 14-3-3σ gene was detected in 93.2%(41/44) of the HCC tissues,56.1%(23/41)of cirrhotic tissues and 6.8%(3/41) of cancer-adjacent tissues,no significant difference between different clinical pathological features,such as gendre,differentiation and HBV infection status.mRNA expression of 14-3-3σ in tissues without methylated product approximated to the normal level,whereas,that in 58/64(90.6%) of samples with methylated product were lower than the detection limit,10.4% were lower than the normal level.The expression and methylation of 14-3-3σ were negatively correlated(P0.05).Conclusion These results indicate that hypermethylation plays a causal role in inactivation of the 14-3-3σ gene in HCC.Hypermethylation and the resulting loss of expression of the 14-3-3σ gene corresponds to one of the most common abnormalities reported to date in HCC,suggesting their crucial role in the development of HCC.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate promoter methylation status,mRNA expression of 14-3-3σ gene and their relationship in hepatocellular carcinoma(HCC).Methods The methylation status of the 14-3-3σ gene in tissues were detected with methylation-specific PCR.The 14-3-3σ mRNA expression was examined by real-time PCR.Results Hypermethylation of CpG islands of the 14-3-3σ gene was detected in 93.2%(41/44) of the HCC tissues,56.1%(23/41)of cirrhotic tissues and 6.8%(3/41) of cancer-adjacent tissues,no significant difference between different clinical pathological features,such as gendre,differentiation and HBV infection status.mRNA expression of 14-3-3σ in tissues without methylated product approximated to the normal level,whereas,that in 58/64(90.6%) of samples with methylated product were lower than the detection limit,10.4% were lower than the normal level.The expression and methylation of 14-3-3σ were negatively correlated(P0.05).Conclusion These results indicate that hypermethylation plays a causal role in inactivation of the 14-3-3σ gene in HCC.Hypermethylation and the resulting loss of expression of the 14-3-3σ gene corresponds to one of the most common abnormalities reported to date in HCC,suggesting their crucial role in the development of HCC.
Key concepts: Hepatocellular carcinoma, Methylation, DNA methylation, CpG site, Gene, Gene expression, Messenger RNA, Biology