High-Throughput Sequencing of Plasma MicroRNA in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis

被引:35
|
作者
Brenu, Ekua W. [1 ,2 ]
Ashton, Kevin J. [3 ]
Batovska, Jana [3 ]
Staines, Donald R. [2 ,4 ]
Marshall-Gradisnik, Sonya M. [1 ,2 ]
机构
[1] Griffith Univ, Griffith Hlth Ctr, Sch Med Sci, Gold Coast, Qld, Australia
[2] Griffith Univ, Natl Ctr Neuroimmunol & Emerging Dis, Gold Coast, Qld, Australia
[3] Bond Univ, Fac Hlth Sci & Med, Robina, Qld, Australia
[4] Queensland Hlth, Gold Coast Publ Hlth Unit, Gold Coast, Qld, Australia
来源
PLOS ONE | 2014年 / 9卷 / 09期
关键词
BLOOD MONONUCLEAR-CELLS; DIFFERENTIAL EXPRESSION; CIRCULATING MICRORNAS; POTENTIAL BIOMARKERS; GENE-EXPRESSION; DOWN-REGULATION; CANCER; IMMUNE; RNA; APOPTOSIS;
D O I
10.1371/journal.pone.0102783
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: MicroRNAs (miRNAs) are known to regulate many biological processes and their dysregulation has been associated with a variety of diseases including Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME). The recent discovery of stable and reproducible miRNA in plasma has raised the possibility that circulating miRNAs may serve as novel diagnostic markers. The objective of this study was to determine the role of plasma miRNA in CFS/ME. Results: Using Illumina high-throughput sequencing we identified 19 miRNAs that were differentially expressed in the plasma of CFS/ME patients in comparison to non-fatigued controls. Following RT-qPCR analysis, we were able to confirm the significant up-regulation of three miRNAs (hsa-miR-127-3p, hsa-miR-142-5p and hsa-miR-143-3p) in the CFS/ME patients. Conclusion: Our study is the first to identify circulating miRNAs from CFS/ME patients and also to confirm three differentially expressed circulating miRNAs in CFS/ME patients, providing a basis for further study to find useful CFS/ME biomarkers.
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页数:8
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