Down-regulation of thyroid hormone receptor β1 gene expression in gastric cancer involves promoter methylation

被引:7
|
作者
Ling, Yaqin [1 ]
Shi, Xiangqun [2 ]
Wang, Yong [2 ]
Ling, Xiaoling [3 ]
Li, Qing [1 ]
机构
[1] Lanzhou Univ, Coll Basic Med, Dept Pathophysiol, Lanzhou 730020, Gansu, Peoples R China
[2] Lanzhou Mil Command PLA, Lanzhou Gen Hosp, Lanzhou 730050, Gansu, Peoples R China
[3] Lanzhou Univ, Hosp 1, Lanzhou 730020, Gansu, Peoples R China
关键词
Gastric cancer; Promoter methylation; Thyroid hormone receptor beta 1; Quantitative methylation-specific PCR (Q-MSP); DNA METHYLATION; HETEROZYGOSITY; RAS; HYPERMETHYLATION; ASSOCIATION; PROTEIN; COLON;
D O I
10.1016/j.bbrc.2014.01.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypermethylation has been shown in the promoter region of the thyroid hormone receptor beta 1 (TR beta 1) gene in several human tumors. However, its role in gastric cancer formation is still unclear. In the study, we analyzed mRNA expression of TR beta 1 gene using real-time quantitative PCR (qPCR). A quantitative methylation-specific PCR (Q-M5P) assay was used to determine the methylation status of the TR beta 1 gene promoter region in 46 pair-matched gastric neoplastic and adjacent non-neoplastic tissues. The results showed that TR beta 1 mRNA expression was significantly reduced in gastric cancer specimens. The methylation of promoter of TR beta 1 gene in gastric cancer tissues was significantly higher than in adjacent normal tissues. Promoter hypermethylation of the TRIM gene correlated with tumor infiltration, lymph node metastasis, and distant metastasis, but it was not associated with other clinicopathological characteristics. We treated gastric cancer cell lines MKN-45, MKN-28, SGC-7901, NCI-N87, and SNU-1 with 5-Aza-2-deoxycytidine (5-Aza-dC). The results showed the expression of TR beta 1 mRNA was increased in MKN-45, MKN-28, SGC-7901, but not increased in NCI-N87 and SNU-1. These results suggest that the TR beta 1 gene plays important roles in the development of gastric cancer partially through epigenetic mechanisms. (C) 2014 Elsevier Inc. All rights reserved.
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页码:147 / 152
页数:6
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