Qian Cheng, Yan Wenying, Li Tengda, Cui Qingya, Liu Peng, Gu Mingli, Guo Jie, Zhang Weiwei, Ren Chuanlu, Wu Tianqin, Deng Anmei
Center for Systems Biology, Soochow University, Suzhou, China.
The 100th Hospital of PLA, Suzhou, China.
Cell Physiol Biochem. 2018;45(1):301-318. doi: 10.1159/000486811. Epub 2018 Jan 19.
BACKGROUND/AIMS: MicroRNAs (miRNAs) have been described to have important roles in primary immune thrombocytopenia (ITP). To gain additional understanding, we have now further evaluated the involvement of miRNAs in ITP.
Microarray experiments were performed to examine the expression profiles of miRNAs and mRNAs in samples from subjects with newly diagnosed ITP (G1), chronic ITP (G2), and normal controls. The systematic Pipeline of Outlier MicroRNA Analysis framework was applied to identify key miRNAs expressed in the G1 and G2 samples. Quantitative PCR and receiver operator characteristic curves were used to confirm the performance of key miRNAs.
Compared with normal controls, 14 miRNAs (12 over-expressed and 2 under-expressed) and 7 over-expressed miRNAs were identified as key in G1 and G2 samples, respectively. miR-106b-5p, miR-200c-3p, and miR-92a-3p exhibited significantly different expression profiles among the groups. In particular, miR-106b-5p and miR-200c-3p were expressed at higher levels in patients with ITP compared to the normal controls. Furthermore, these two miRNAs expressions were even higher in patients with chronic ITP.
MiR-106b-5p and miR-200c-3p may represent valuable biomarkers of ITP, although further studies are needed to confirm and assess the value of these potential biomarkers at various stages of ITP.
背景/目的:微小RNA(miRNA)已被描述在原发性免疫性血小板减少症(ITP)中发挥重要作用。为了进一步了解,我们现在进一步评估了miRNA在ITP中的作用。
进行微阵列实验以检测新诊断的ITP患者(G1组)、慢性ITP患者(G2组)和正常对照样本中miRNA和mRNA的表达谱。应用异常微小RNA分析框架的系统流程来鉴定在G1和G2样本中表达的关键miRNA。使用定量PCR和受试者工作特征曲线来确认关键miRNA的性能。
与正常对照相比,分别在G1和G2样本中鉴定出14个miRNA(12个过表达和2个低表达)和7个过表达的miRNA为关键miRNA。miR-106b-5p、miR-200c-3p和miR-92a-3p在各组之间表现出显著不同的表达谱。特别是,与正常对照相比,ITP患者中miR-106b-5p和miR-200c-3p的表达水平更高。此外,这两种miRNA在慢性ITP患者中的表达甚至更高。
MiR-106b-5p和miR-200c-3p可能代表ITP的有价值生物标志物,尽管需要进一步研究来确认和评估这些潜在生物标志物在ITP各个阶段的价值。