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miRNA-221作为肝细胞癌新型预后生物标志物的临床潜力

Clinical potential of miRNA-221 as a novel prognostic biomarker for hepatocellular carcinoma.

作者信息

Chen Fan, Li Xin-Feng, Fu Dong-Sheng, Huang Jian-Guo, Yang Shun-E

机构信息

Department of Oncology, Urumqi General Hospital of Lanzhou Military Command of PLA, Urumqi, Xinjiang, China.

Department of Surgery, The Sixth Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.

出版信息

Cancer Biomark. 2017;18(2):209-214. doi: 10.3233/CBM-161671.

Abstract

miRNA-221 is one of the over 700 kinds of currently known microRNAs (miRNAs) and is up-regulated in multiple tumors, suggesting that it may be a potential carcinogenic miRNA. Few studies have explored the relationship between miRNA-221 and hepatocellular carcinoma (HCC). We performed real-time quantitative polymerase chain reaction (qPCR) to detect miRNA-221 expression in HCC and para-carcinoma tissues and to explore the relationship between abnormal expression of miRNA-221 and clinicopathological features of HCC patients. miRNA-221 expression was significantly higher in HCC tissues than in adjacent tissues (P < 0.001). We analyzed the relationship between miRNA-221 expression level and clinicopathological characteristics of HCC patients. Our results suggested that miRNA-221 expression level was closely related to tumor stage (P = 0.012), number of tumor nodes (P = 0.018), and microvascular invasion (P = 0.010) in HCC patients. The results of survival analysis suggested that HCC patients with up-regulated miRNA-221 expression had a shorter survival time. The high miRNA-221 expression indicates the poor prognosis of HCC patients; thus, miRNA-221 can be regarded an important molecular marker for HCC prognosis.

摘要

微小RNA-221是目前已知的700多种微小RNA(miRNA)之一,在多种肿瘤中呈上调表达,提示其可能是一种潜在的致癌性miRNA。很少有研究探讨微小RNA-221与肝细胞癌(HCC)之间的关系。我们进行了实时定量聚合酶链反应(qPCR),以检测HCC组织和癌旁组织中微小RNA-221的表达,并探讨微小RNA-221的异常表达与HCC患者临床病理特征之间的关系。微小RNA-221在HCC组织中的表达显著高于相邻组织(P < 0.001)。我们分析了微小RNA-221表达水平与HCC患者临床病理特征之间的关系。我们的结果表明,微小RNA-221表达水平与HCC患者的肿瘤分期(P = 0.012)、肿瘤结节数量(P = 0.018)和微血管侵犯(P = 0.010)密切相关。生存分析结果表明,微小RNA-221表达上调的HCC患者生存时间较短。微小RNA-221高表达提示HCC患者预后较差;因此,微小RNA-221可被视为HCC预后的重要分子标志物。

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