Fu Zhengchuan, Qian Fang, Yang Xuhuan, Jiang Hailiang, Chen Yu, Liu Sihai
Department of Oncology, Zaozhuang Mining Group Central Hospital, Qilianshan Road, Zaozhuang, 277000, Shandong, China,
Med Oncol. 2014 Sep;31(9):164. doi: 10.1007/s12032-014-0164-8. Epub 2014 Aug 17.
Previous studies have revealed the significance of circulating microRNAs as biomarkers for cancers. The aim of this study was to detect the levels of circulating microRNA-222 (miR-222) in plasma of gastric cancer (GC) patients and evaluate its diagnostic and prognostic value. Levels of circulating miR-222 were detected by using qRT-PCR in plasma of 114 GC patients, 36 chronic atrophic gastritis (CAG) patients and 56 healthy controls. The result showed that the expression of circulating miR-222 in plasma was significantly upregulated in GC compared with CAG and healthy controls (all at P < 0.001). And its high level was significantly correlated with clinical stages (P < 0.001) and lymph nodes metastasis (P = 0.009). The receiver operating characteristics (ROC) curve analyses revealed that miR-222 had considerable diagnostic accuracy, yielded an AUC (the areas under the ROC curve) of 0.850 with 66.1 % sensitivity and 88.3 % specificity in discriminating GC from healthy controls. Moreover, Kaplan-Meier analysis demonstrated a correlation between increased circulating miR-222 level and reduced disease-free survival (P = 0.016) and overall survival (P = 0.012). In multivariate analysis stratified for known prognostic variables, circulating miR-222 was identified as an independent prognostic marker. In conclusion, our findings suggested that circulating miR-222 in plasma might be a potential and useful noninvasive biomarker for the early detection and prognosis of GC.
既往研究已揭示循环微小RNA作为癌症生物标志物的重要性。本研究旨在检测胃癌(GC)患者血浆中循环微小RNA-222(miR-222)的水平,并评估其诊断和预后价值。采用qRT-PCR检测114例GC患者、36例慢性萎缩性胃炎(CAG)患者和56例健康对照者血浆中循环miR-222的水平。结果显示,与CAG患者和健康对照相比,GC患者血浆中循环miR-222的表达显著上调(均P<0.001)。其高水平与临床分期(P<0.001)和淋巴结转移(P=0.009)显著相关。受试者工作特征(ROC)曲线分析显示,miR-222具有相当高的诊断准确性,在区分GC与健康对照时,曲线下面积(AUC)为0.850,灵敏度为66.1%,特异性为88.3%。此外,Kaplan-Meier分析表明,循环miR-222水平升高与无病生存期缩短(P=0.016)和总生存期缩短(P=0.012)相关。在对已知预后变量进行分层的多变量分析中,循环miR-222被确定为独立的预后标志物。总之,我们的研究结果表明,血浆中循环miR-222可能是GC早期检测和预后的一种潜在且有用的非侵入性生物标志物。