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作 者:邱冬妮[1,2] 张骏[1,2] 陈坚[1,2] 蒋蔚茹[1,2] 黄剑平[1,2] 蒋晓芸[1,2] 裴晓宇[1,2] 刘杰[1,2]
机构地区:[1]复旦大学附属华山医院消化内科 [2]复旦大学消化病研究所,上海200040
出 处:《国际消化病杂志》2014年第4期275-277,共3页International Journal of Digestive Diseases
基 金:上海市卫生局科研项目(2010Y057)
摘 要:目的研究microRNA let-7a(以下简称let-7a)对乙型肝炎病毒(HBV)复制的影响。方法 (1)收集23例伴有慢性活动性乙型肝炎的肝细胞癌(HCC)患者的手术标本,用实时荧光定量PCR(real-time qRT-PCR)检测let-7a在HCC组织中的表达,分析let-7a的表达和HBV复制状态之间的关系。(2)用real-time qRT-PCR法检测HBV稳定复制的HCC细胞系HepG2.2.15及其亲本HCC细胞HepG2的let-7a表达。(3)通过细胞转染,利用let-7a特异的反义寡核苷酸抑制物下调HepG2.2.15细胞中let-7a的表达,通过实时PCR(real-time PCR)检测HBV DNA水平的变化。结果 let-7a在HBV高复制的临床HCC标本中明显高于HBV低复制者(P<0.05)。与HepG2相比,let-7a在HBV稳定复制的HepG2.2.15细胞系中表达上调(P<0.05)。let-7a抑制剂能显著抑制HBV DNA的水平,并且具有时间依赖性(P<0.05)。结论 let-7a的表达和HBV的复制状态呈正相关,let-7a能促进HBV复制。Objective To investigate the effect of microRNA let-7a on replication of HBV. Methods (1) To detect let-7a with real-time qRT-PCR in 23 liver cancer samples with active chronic hepatitis B, and explore the relationship between let-7a level and HCV replication. (2) To detect let-7a with real-time qRT-PCR in HepG2.2. 15 and HepG2. (3) The specific antisense inhibitor for lev7a was transfected into HepG2.2. 15 cells to down-regulate its expression, and detect HBV DNA with real-time PCR. Results The level of let-7a was significantly higher in liver cancer samples in HBV high replicated rate than that in HBV low replicated rate (P〈0. 05). The level of let-7a was significantly higher in HepG2.2.15 than that in HepG2 (P〈0.05). The specific antisense inhibitor for let-7a inhibited HBV replication on HBV DNA levels (P〈0.05). Conclusions The expression of let-7a has a positive relationship with the replication of HBV. Then, let-7a can promote HBV replication.
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