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Identification of microRNAs Specifically Expressed in Hepatitis C Virus-Associated Hepatocellular Carcinoma

机译:在丙型肝炎病毒相关肝细胞癌中特异性表达的MicroRNA的鉴定

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摘要

Although several studies have investigated the association of miRNAs with hepatocellular carcinoma (HCC), the data published so far are not concordant. A reason for these discrepancies may be the fact that most studies used as a control the non-tumorous tissue surrounding the HCC lesion, which is almost invariably affected by cirrhosis or chronic hepatitis, as well as other pathological conditions such as hepatitis B virus (HBV) or hepatitis C virus (HCV) infection. Moreover, HCC is often analyzed as a single group regardless of the different viral etiologies. In this study, we investigated miRNAs differentially expressed in HCV-related HCC by comparing the tumorous tissues to a wide range of liver specimens, including healthy livers obtained from liver donors and patients who underwent liver resection for angioma, in addition to tissues from various acute and chronic liver diseases, including HCV-related cirrhosis not associated with HCC, HCV-related cirrhosis associated with HCC, and HBV-associated acute liver failure (ALF). Our study examined the whole set of 2,226 human miRNAs, including 1,121 pre miRNAs and 1,105 mature miRNAs, available in a microarray platform.Stringent statistical methods were applied to reduce the risk of false discoveries to less than 1%. Our data identified 18 miRNAs exclusively expressed in HCV-associated HCC, characterized by high specificity and selectivity versus all other liver diseases and healthy conditions, and connected into a regulatory network pivoting on p53, phosphatase and tensin homolog (PTEN), and all-trans retinoic acid signaling.
机译:尽管有几项研究调查了miRNA与肝细胞癌(HCC)的关联,但迄今为止发表的数据并不一致。这些差异的原因可能是因为大多数研究都将HCC病灶周围的非肿瘤组织用作对照,这一事实几乎总是受到肝硬化或慢性肝炎以及其他病理状况如乙型肝炎病毒(HBV)的影响)或丙型肝炎病毒(HCV)感染。此外,无论病毒病因如何,经常将HCC分为一组进行分析。在这项研究中,我们通过比较肿瘤组织与各种肝脏标本(包括从肝供体获得的健康肝脏和接受血管瘤切除术的患者)以及各种急性组织中的肿瘤组织,研究了在HCV相关HCC中差异表达的miRNA。慢性肝病,包括与HCC不相关的HCV相关性肝硬化,与HCC相关的HCV相关性肝硬化以及HBV相关的急性肝衰竭(ALF)。我们的研究检查了微阵列平台上可用的整套2226种人类miRNA,包括1,121个pre miRNA和1,105个成熟miRNA,并采用严格的统计方法将错误发现的风险降低到不足1%。我们的数据鉴定出18种仅在HCV相关HCC中表达的miRNA,与所有其他肝脏疾病和健康状况相比,其特点是高特异性和选择性,并连接到以p53,磷酸酶和张力蛋白同源物(PTEN)和全反式为中心的调控网络中视黄酸信号。

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