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首页|期刊导航|南京医科大学学报(自然科学版)|DNA甲基化异常对mir-615-5p在胰腺癌细胞株PANC-1中表达影响

DNA甲基化异常对mir-615-5p在胰腺癌细胞株PANC-1中表达影响

朱墨 高文涛 钱祝银 苗毅

南京医科大学学报(自然科学版)2011,Vol.31Issue(1):26-30,5.
南京医科大学学报(自然科学版)2011,Vol.31Issue(1):26-30,5.

DNA甲基化异常对mir-615-5p在胰腺癌细胞株PANC-1中表达影响

Abnormal DNA methylation in pancreatic cancer cell line PANC-1 affects mir-615-5p expression

朱墨 1高文涛 1钱祝银 1苗毅1

作者信息

  • 1. 南京医科大学第一附属医院胆胰外科,江苏南京210029
  • 折叠

摘要

Abstract

Objective: To observe the abnormal DNA methylation inhibits the miRNA expression in pancreatic cancer cell line,and DNA methyltransferase inhibitor on the miR-615-5p of the methylation status and expression in the pancreatic cancer cell line PANC-1. Methods: Methylation microarray was used to screen in pancreatic cancer cell line PANC-1 in the abnormal methylation of miRNA. PANC-1 cells were treated with demethylating agent 5-aza-2-adeoxycytidine (5-aza-dC) in vitro, Methylation specific polymerase chain reaction (methyla-tion- specific PCR, MSP) combination of bisulfite modified DNA sequencing method (bisulfite-sequencing PCR, BSP) were used to detect miR-615-5p methylation changes before and after treatment. The changes of miR-615-5p expression was detected by quantitative RT-PCR before and after treatment. Results: Methylation was significanfiy higher in pancreatic cancer cell line PANC-1 than in normal tissue by MSP and BSP methods. miR-615-5p reduction in methylation was associated with the expression reactivation in the pancreatic cancer cells PANC-1 treated with demethylation agent 5-asa-dC. Condlusion: This study demonstrates that aberrant DNA methylation of the miR-615-5p CpG island is closely linked to their inappropriate silencing in pancreatic cancer cell line PANC-1.

关键词

DNA甲基化/miR-615-5p胰腺癌/5-氮杂胞苷

Key words

DNA methylation/ miR-615-5p/ pancreatic cancer/ 5-aza-dC

分类

生物科学

引用本文复制引用

朱墨,高文涛,钱祝银,苗毅..DNA甲基化异常对mir-615-5p在胰腺癌细胞株PANC-1中表达影响[J].南京医科大学学报(自然科学版),2011,31(1):26-30,5.

基金项目

江苏省自然科学基金(BK2006241) (BK2006241)

国家自然科学基金(30500492) (30500492)

南京医科大学学报(自然科学版)

OA北大核心CSCDCSTPCD

1007-4368

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