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A Circulating MicroRNA Signature Capable of Assessing the Risk of Hepatocellular Carcinoma in Cirrhotic Patients

机译:能够评估肝硬化患者肝细胞癌风险的循环微瘤签名

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摘要

Abstract With the availability of potent antiviral therapies, complete suppression of hepatitis B virus (HBV) replication and total eradication of hepatitis C virus (HCV) can now be achieved. Despite these advances, hepatocellular carcinoma (HCC) still develops in a substantial proportion of cirrhotic patients, suggesting that host factors remain critical. Dysregulation of miRNAs is noted in many cancers, and circulating miRNAs can be readily assayed. In this study, we aimed to develop a circulating miRNA signature to assess the risk of HCC in cirrhotic patients. We first discovered that HBV- and HCV-related cirrhotic patients had distinguishable circulating miRNA profiles. A cohort of 330 cirrhotic patients was then compared against a cohort of 42 early HCC patients with complete remission. A score comprising 5 miRNAs and a binary etiology variable was established that was capable of differentiating between these two groups (AUC = 72.5%, P < 0.001). The 330 cirrhotic patients were further stratified into high- and low-risk groups, and all patients were longitudinally followed for 752 (11–891) days. Of them, 19 patients developed HCC. The high-risk group had significantly higher cumulative HCC incidence (P = 0.038). In summary, a circulating miRNA-based score was developed that is capable of assessing HCC risks in cirrhotic patients.
机译:摘要现在可以实现有效抗病毒疗法的可用性,完全抑制乙型肝炎病毒(HBV)复制和完全根除丙型肝炎病毒(HCV)。尽管有这些进步,但肝细胞癌(HCC)仍然以大量比例的肝硬化患者发展,这表明宿主因素仍然是至关重要的。在许多癌症中注意到miRNA的失调,并且可以容易地测定循环miRNA。在这项研究中,我们旨在开发循环miRNA签名,以评估肝硬化患者HCC的风险。我们首先发现HBV和HCV相关的肝硬化患者具有可区分的循环miRNA型材。然后将330名肝硬化患者的队列与42例早期HCC患者进行了完全缓解的群组。建立了包含5 miRNA和二元病因变量的分数,其能够区分这两组(AUC = 72.5%,P <0.001)。将330名肝硬化患者进一步分解为高风险群体,所有患者均纵向持续752(11-891)天。其中,19名患者开发出HCC。高风险组累积HCC发病率明显较高(P = 0.038)。总之,开发了基于循环的基于MiRNA的评分,其能够评估肝硬化患者的HCC风险。

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