Yamamoto Yusuke, Kondo Shunsuke, Matsuzaki Juntaro, Esaki Minoru, Okusaka Takuji, Shimada Kazuaki, Murakami Yoshiki, Enomoto Masaru, Tamori Akihiro, Kato Ken, Aoki Yoshiaki, Takizawa Satoko, Sakamoto Hiromi, Niida Shumpei, Takeshita Fumitaka, Ochiya Takahiro
Division of Molecular and Cellular Medicine National Cancer Center Research Institute Tokyo Japan.
Department of Hepatobiliary and Pancreatic Oncology National Cancer Center Hospital Tokyo Japan.
Hepatol Commun. 2019 Dec 19;4(2):284-297. doi: 10.1002/hep4.1451. eCollection 2020 Feb.
Hepatocellular carcinoma (HCC) is the fourth leading cause of cancer deaths worldwide. The high mortality rate in HCC is largely due to the difficulty of early detection. In this study, to improve patient outcomes, serum samples from 345 patients with HCC, 46 patients with chronic hepatitis (CH), 93 patients with liver cirrhosis (LC), and 1,033 healthy individuals were analyzed with microRNA (miRNA) microarrays. We investigated the diagnostic potential of circulating miRNAs in serum and developed a detection model of HCC, including early stage. A diagnostic model was constructed based on the expression levels of a combination of miRNAs in a discovery set. We selected 52 miRNAs that had altered expressions according to disease progression status, established the diagnostic model with a combination of eight miRNAs in the discovery set, and tested the model in a validation set. The diagnostic values for discriminating cancer from HCC at-risk control samples were as follows: area under the curve, 0.99; sensitivity, 97.7%; specificity, 94.7%. With this model, 98% of stage I HCC cases were detected; these results were much better than those observed from conventional methods. Circulating miRNAs could serve as biomarkers for the accurate detection of HCC. Because the diagnostic accuracy was maintained even in stage I, this may represent an accurate detection method even for early stage HCC.
肝细胞癌(HCC)是全球第四大致癌死亡原因。HCC的高死亡率主要归因于早期检测的困难。在本研究中,为改善患者预后,我们使用微小RNA(miRNA)微阵列分析了345例HCC患者、46例慢性肝炎(CH)患者、93例肝硬化(LC)患者以及1033名健康个体的血清样本。我们研究了血清中循环miRNA的诊断潜力,并开发了一种包括早期阶段的HCC检测模型。基于发现集中miRNA组合的表达水平构建了诊断模型。我们选择了52种根据疾病进展状态表达发生改变的miRNA,在发现集中用8种miRNA的组合建立了诊断模型,并在验证集中对该模型进行了测试。区分癌症与HCC风险对照样本的诊断价值如下:曲线下面积为0.99;敏感性为97.7%;特异性为94.7%。使用该模型,98%的I期HCC病例被检测到;这些结果比传统方法观察到的结果要好得多。循环miRNA可作为准确检测HCC的生物标志物。由于即使在I期也能保持诊断准确性,这可能代表了一种即使对于早期HCC也准确的检测方法。