Chen Hankui, Liu Helu, Zou Hanqing, Chen Rui, Dou Yuhong, Sheng Shile, Dai Shengming, Ai Junmei, Melson Joshua, Kittles Rick A, Pirooznia Mehdi, Liptay Michael J, Borgia Jeffrey A, Deng Youping
1. Rush University Cancer Center, Chicago, IL 60612;
1. Rush University Cancer Center, Chicago, IL 60612;; 8. Shenzhen Baoan District Shajing Hospital, Shenzhen, Guangdong 518104, China.
J Cancer. 2016 Feb 5;7(5):490-9. doi: 10.7150/jca.12351. eCollection 2016.
Stable blood based miRNA species have allowed for the differentiation of patients with various types of cancer. Therefore, specific blood-based miRNA might be considered as a methodology which could be informative of the presence of cancer potentially from multiple distinct organ sites. Recently, miR-21 has been identified as an "oncomir" in various tumors while miR-152 as a tumor suppressor. In this study, we investigated whether circulating miR-21 and miR-152 can be used for early detection of lung cancer (LuCa), colorectal carcinoma (CRC), breast cancer (BrCa) and prostate cancer (PCa), with distinguishing cancer from various benign lesions on these organ sites. We measured the two miRNA levels by using real-time RT-PCR in plasma samples from a total of 204 cancer patients, 159 various benign lesions, and 228 normal subjects. We observed significantly elevated expression of miR-21 and miR-152 in LuCa, CRC, and BrCa when compared with normal controls. We also found upregulation of plasma miR-21 and miR-152 levels in patients with benign lesions of lung and breast, as compared to normal controls, respectively. No significant expression variation of the two miRNAs was observed in PCa or prostatic benign lesions as compared to healthy controls. Receiver operating characteristic (ROC) analyses revealed that miR-21 and/or miR-152 can discriminate LuCa, CRC and BrCa from normal controls. Our results suggest that plasma miR-21 and miR-152 may serve as non-specific noninvasive biomarkers for early screening of LuCa, CRC, and BrCa, but not PCa.
血液中稳定的微小RNA(miRNA)种类有助于区分患有各种癌症的患者。因此,特定的血液miRNA可被视为一种方法,它可能有助于了解多个不同器官部位潜在的癌症存在情况。最近,miR-21已被确定为多种肿瘤中的“癌基因miRNA”,而miR-152则是一种肿瘤抑制因子。在本研究中,我们调查了循环miR-21和miR-152是否可用于肺癌(LuCa)、结直肠癌(CRC)、乳腺癌(BrCa)和前列腺癌(PCa)的早期检测,并区分这些器官部位的各种良性病变与癌症。我们使用实时逆转录聚合酶链反应(RT-PCR)测量了总共204例癌症患者、159例各种良性病变患者和228例正常受试者血浆样本中的这两种miRNA水平。我们观察到,与正常对照组相比,LuCa、CRC和BrCa中miR-21和miR-152的表达显著升高。我们还发现,与正常对照组相比,肺和乳腺良性病变患者血浆miR-21和miR-152水平分别上调。与健康对照组相比,在PCa或前列腺良性病变中未观察到这两种miRNA的显著表达变化。受试者工作特征(ROC)分析显示,miR-21和/或miR-152可将LuCa、CRC和BrCa与正常对照组区分开来。我们的结果表明,血浆miR-21和miR-152可能作为非特异性非侵入性生物标志物用于LuCa、CRC和BrCa的早期筛查,但不能用于PCa。