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原发性胆汁性胆管炎患者血浆中环状RNA的基因芯片表达谱

Microarray Expression Profile of Circular RNAs in Plasma from Primary Biliary Cholangitis Patients.

作者信息

Zheng Jiajia, Li Zhenrong, Wang Tiancheng, Zhao Yang, Wang Yongfeng

机构信息

Department of Laboratory Medicine, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, China.

Department of Laboratory Medicine, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, China.

出版信息

Cell Physiol Biochem. 2017;44(4):1271-1281. doi: 10.1159/000485487. Epub 2017 Nov 29.

Abstract

BACKGROUND/AIMS: Circular RNAs (circRNAs) play a crucial role in the occurrence of several diseases, including autoimmune diseases. However, their role in primary biliary cholangitis (PBC) remains unclear. Here, we aimed to determine the circRNA expression profile in plasma from PBC patients and further explore the value of circRNA in diagnosing PBC.

METHODS

CircRNA microarrays were used to determine circRNA expression profiles in plasma samples from 6 PBC patients and 6 healthy controls. Statistical analyses identified differentially expressed circRNAs, and these circRNAs were verified by qRT-PCR in 29 PBC patients and 30 healthy controls. MicroRNA (miRNA) target prediction software identified putative miRNA response elements (MREs), which were used to construct a map of circRNA-miRNA interactions for the differentially expressed circRNAs.

RESULTS

Our results indicated that there were 18 up-regulated and 4 down-regulated circular RNAs in the plasma from PBC patients compared with that from healthy individuals. Among the differentially expressed circRNAs, hsa_circ_402458 (P=0.0033), hsa_circ_087631 and hsa_circ_406329 (P=0.0185) were up-regulated, and hsa_circ_407176 (P=0.0066) and hsa_circ_082319 were down-regulated in the PBC group versus the healthy group as demonstrated by qRT-PCR. In particular, hsa_circ_402458 was significantly higher in PBC patients not receiving UDCA treatment than in PBC patients receiving UDCA treatment (P=0.0338). The area under the receiver operating characteristic curve for hsa_circ_402458 for diagnosing PBC was 0.710 (P=0.005). For hsa_circ_402458, two putative miRNA targets, hsa-miR-522-3p and hsa-miR-943, were predicted.

CONCLUSIONS

circRNA dysregulation may play a role in PBC pathogenesis, and hsa_circ_402458 shows promise as a candidate biomarker for PBC.

摘要

背景/目的:环状RNA(circRNAs)在包括自身免疫性疾病在内的多种疾病发生中起关键作用。然而,它们在原发性胆汁性胆管炎(PBC)中的作用仍不清楚。在此,我们旨在确定PBC患者血浆中的circRNA表达谱,并进一步探索circRNA在诊断PBC中的价值。

方法

使用circRNA微阵列确定6例PBC患者和6例健康对照血浆样本中的circRNA表达谱。统计分析确定差异表达的circRNAs,并通过qRT-PCR在29例PBC患者和30例健康对照中对这些circRNAs进行验证。微小RNA(miRNA)靶标预测软件识别推定的miRNA反应元件(MREs),用于构建差异表达circRNAs的circRNA-miRNA相互作用图谱。

结果

我们的结果表明,与健康个体相比,PBC患者血浆中有18种环状RNA上调,4种下调。在差异表达circRNAs中,qRT-PCR显示,与健康组相比,PBC组中hsa_circ_402458(P = 0.0033)、hsa_circ_087631和hsa_circ_406329(P = 0.0185)上调,hsa_circ_40

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