miR-21/PTEN/E-Cadherin对慢性HCV感染不同阶段上皮-间质转化的干扰

Yasser B. M. Ali, M. Thabet, Abeer S. El-Maghraby, A. Gomaa, O. Khamiss, R. Talaat
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摘要

肝细胞癌(HCC)是与丙型肝炎病毒感染(HCV)相关的主要并发症。上皮-间质转化(epithelial-mesenchymal transition, EMT)是HCC侵袭和转移的关键。一些microrna (mirna)与hcv相关的HCC有关。本研究旨在评价miR-21、磷酸酶、10号染色体上缺失的紧张素同源物(PTEN)和E-Cadherin在HCV感染不同阶段EMT过程中的作用。研究了100例hcv感染患者,其中75例为hcv诱导的肝硬化(分为Child A、B、C), 25例为HCC。与此同时,45名健康志愿者被视为正常对照。采用定量逆转录聚合酶链反应(qRT-PCR)检测循环mir -21。采用酶联免疫吸附试验(ELISA)检测血清PTEN和e-钙粘蛋白水平。与对照组相比,HCC患者的miR-21水平明显升高(P值小于0.01)。肝细胞癌患者的E-cadherins和PTEN水平较肝硬化和正常人最低(P<0.01)。在HCC患者中,PTEN与E-cadherin呈正相关(r= 0.501;p < 0.01)。另一方面,miR-21与两种E-cadherins呈负相关(r= -0.455;p<0.01)和PTEN (r= -0.255;P <0.05)。因此,肿瘤中miR-21的上调是hcv阳性肝硬化肝癌发生的重要步骤,并可能导致PTEN和E-cadherin的下调,从而促进肿瘤的发生。我们的数据可能是第一个将miR-21、PTEN和E-cadherin在HCV感染的不同阶段(从肝硬化到HCC)联系起来的研究。
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Interference between miR-21/PTEN/E-Cadherin and Epithelial-Mesenchymal Transition in Various Stages of Chronic HCV Infection
Hepatocellular carcinoma (HCC) is a major complication associated with hepatitis C viral infection (HCV). The epithelial-mesenchymal transition (EMT) is critical in HCC invasion and metastasis. Several m icroRNAs (miRNAs) have been linked to HCV-related HCC. This study aimed to evaluate the relation between miR-21, phosphatase, tensin homolog deleted on chromosome ten (PTEN), and E-Cadherin with a flashlight on their role in the EMT process in HCV infection at different stages. One hundred HCV-infected patients were studied, 75 had HCV-induced cirrhosis (classified into Child A, B, and C), and 25 had HCC. In parallel, 45 healthy volunteers were considered normal controls. Circulating miR-21was detected by quantitative Reverse Transcription Polymerase Chain Reaction (qRT–PCR).PTEN and E-cadherin serum levels were measured using Enzyme-Linked Immunosorbent Assay (ELISA). A significant elevation in miR-21 was observed in HCC patients compared with control ones(P˂0.01). HCC patients had the lowest E-cadherins and PTEN (P<0.01) compared with cirrhotic and normal subjects. In HCC patients, PTEN was positively correlated with E-cadherin (r= 0.501; p<0.01). On the other hand, a negative correlation between miR-21 and both E-cadherins (r= -0.455; p<0.01) and PTEN (r= -0.255; p<0.05) was observed. Accordingly, up-regulation of miR-21 in the tumor is an important step in HCV-positive cirrhotic hepatocarcinogenesis and might result in concomitant down-regulation of PTEN and E-cadherin in favor of tumor promotion. Our data might be the first study that correlates miR-21, PTEN, and E-cadherin in different stages of HCV infection (from cirrhosis to HCC).
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