In vitro study of relationship between miRNA205 promoter methylation and Barrett’s esophagus cancerous
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In vitro study of relationship between miRNA205 promoter methylation and Barrett’s esophagus cancerous
Journal of Chongqing Medical UniversityVol. 38, Issue 12, Pages: 1708-1712(2014)
作者机构:
重庆医科大学第二附属医院消化内科,重庆,400010
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Published:2014,
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Liu Tianyu, Lyu Lin, Mei Zhechuan, et al. In vitro study of relationship between miRNA205 promoter methylation and Barrett’s esophagus cancerous. [J]. Journal of Chongqing Medical University 38(12):1708-1712(2014)
DOI:
Liu Tianyu, Lyu Lin, Mei Zhechuan, et al. In vitro study of relationship between miRNA205 promoter methylation and Barrett’s esophagus cancerous. [J]. Journal of Chongqing Medical University 38(12):1708-1712(2014)DOI:
In vitro study of relationship between miRNA205 promoter methylation and Barrett’s esophagus cancerous
目的:探讨microRNA205(miR205)启动子甲基化与Barrett食管(Barrett’s esophagus,BE)癌变的关系。方法:运用RT-PCR检测经去甲基化处理前后BE、食管癌和正常食管粘膜细胞中miR205表达水平,采用甲基化特异性聚合酶链式反应(methylation specific polymerase chain reaction,MSP)检测样本中miR205启动子甲基化水平。结果:BE和食管癌细胞miR205表达量较正常食管明显减低(P=0.002);去甲基化处理后,样本miR205表达量水平明显升高(P=0.000)。MSP结果显示BE和食管癌细胞miR205启动子经去甲基化处理后呈低甲基化或非甲基化。结论:miR205在BE和食管癌细胞中表达降低与其启动子甲基化有关,miR205启动子甲基化贯穿了BE的癌变过程,有可能成为BE癌变过程中的关键分子生物学标志,并可能成为预防和治疗BE癌变的靶点。
Abstract
Objective:To explor the relationship between MiR205 promoter methylation and Barrett’s esophagus cancerous. Methods:The expression of miRNA205 in Barrett’s esophagus,esophageal cancer and normal esophageal mucosa cells before and after demethylation processing was detected by RT-PCR. MiR205 promoter methylation levels were measured by methylation specific polymerase chain reaction(MSP). Results:miR205 expression was reduced obviously in Barrett’s esophagus and esophageal cancer cells than in normal esophageal,with statistically significant differences(P=0.002). After demethylation,miR205 expression was sig-nificantly increased in Barrett’s esophagus(BT,B-T10) and esophageal cancer(EC109,TE-10,SEG-1) cells,with statistically sig-nificant differences(P=0.000). MSP showed miR205 promoter changes to be low-methylation or non-methylation. Conclusion:Re-duced expression of miR205 in Barrett’s esophagus and esophageal cancer cells is related to its promoter methylation. Throughout the carcinogenesis of Barrett’s esophagus,miR205 promoter methylation may become a key molecular biomarker in process of Barrett’s esophagus canceration and may become the prevention and treatment targets of Barrett’s esophagus canceration.
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