Yang Jingwen, Dong Weiwei, Zhang He, Zhao Huixia, Zeng Zhiyan, Zhang Fengyun, Li Qiuwen, Duan Xiaohong, Hu Yanyan, Xiao Wenhua
Senior Department of Oncology, The Fifth Medical Center of PLA General Hospital, Beijing, China.
Department of Oncology, 4th Medical Center of PLA General Hospital, Beijing, China.
Front Cell Dev Biol. 2022 Sep 23;10:927251. doi: 10.3389/fcell.2022.927251. eCollection 2022.
Diagnostic tools for hepatocellular carcinoma (HCC) are critical for patient treatment and prognosis. Thus, this study explored the diagnostic value of the exosomal microRNA panel for HCC. Expression profiles of microRNAs in exosomes and plasma of HCC and control groups were assessed using microRNA microarray analysis. Reverse transcription-quantitative PCR was applied to evaluate the expression of candidate microRNAs in blood samples from 50 HCC patients, 50 hepatic cirrhosis patients, and 50 healthy subjects. The area calculated the diagnostic accuracy of the microRNAs and microRNA panel under the receiver operating characteristic curve (AUC). MicroRNA microarray analysis revealed that there were more differentially expressed microRNAs in the exosome HCC group than plasma HCC group. Among the 43 differentially expressed microRNAs contained in both exosomes and plasma, we finally decided to testify the expression and diagnostic significance of microRNA-26a, microRNA-29c, and microRNA-199a. The results indicated that expression of the microRNA-26a, microRNA-29c, and microRNA-199a in both exosomes and plasma was significantly lower in HCC patients compared with hepatic cirrhosis and healthy group. Interestingly, exosomal microRNAs were substantially more accurate in diagnosing HCC than microRNAs and alpha-fetoprotein in plasma. Moreover, the exosomal microRNA panel containing microRNA-26a, microRNA-29c, and microRNA-199a showed high accuracy in discriminating HCC from healthy (AUC = 0.994; sensitivity 100%; specificity 96%) and hepatic cirrhosis group (AUC = 0.965; sensitivity 92%; specificity 90%). This study revealed that the exosomal microRNA panel has high accuracy in diagnosing HCC and has important clinical significance.
肝细胞癌(HCC)的诊断工具对患者的治疗和预后至关重要。因此,本研究探讨了外泌体微小RNA(miRNA)组合对HCC的诊断价值。使用miRNA微阵列分析评估HCC组和对照组外泌体及血浆中miRNA的表达谱。应用逆转录定量PCR评估50例HCC患者、50例肝硬化患者和50例健康受试者血液样本中候选miRNA的表达。计算miRNA及miRNA组合在受试者工作特征曲线(AUC)下的诊断准确性。miRNA微阵列分析显示,外泌体HCC组中差异表达的miRNA比血浆HCC组更多。在同时存在于外泌体和血浆中的43种差异表达miRNA中,我们最终决定验证miR-26a、miR-29c和miR-199a的表达及诊断意义。结果表明,与肝硬化组和健康组相比,HCC患者外泌体和血浆中miR-26a、miR-29c和miR-199a的表达均显著降低。有趣的是,外泌体miRNA在诊断HCC方面比血浆中的miRNA和甲胎蛋白更准确。此外,包含miR-26a、miR-29c和miR-199a的外泌体miRNA组合在区分HCC与健康组(AUC = 0.994;敏感性100%;特异性96%)和肝硬化组(AUC = 0.965;敏感性92%;特异性90%)方面显示出高准确性。本研究表明,外泌体miRNA组合在诊断HCC方面具有高准确性,具有重要的临床意义。