miRNA Expression Profiles and Potential as Biomarkers in Nontuberculous Mycobacterial Pulmonary Disease

被引:22
作者
Han, Sun Ae [1 ]
Jhun, Byung Woo [1 ]
Kim, Su-Young [1 ]
Moon, Seong Mi [1 ]
Yang, Bumhee [1 ]
Kwon, O. Jung [1 ]
Daley, Charles L. [2 ,3 ]
Shin, Sung Jae [4 ]
Koh, Won-Jung [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Div Pulm & Crit Care Med,Sch Med, Seoul, South Korea
[2] Natl Jewish Hlth, Div Mycobacterial & Resp Infect, Dept Med, Denver, CO USA
[3] Univ Colorado, Dept Med, Aurora, CO USA
[4] Yonsei Univ, Coll Med, Brain Korea PLUS Project Med Sci 21, Dept Microbiol,Inst Immunol & Immunol Dis, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
CIRCULATING MICRORNAS; TUBERCULOSIS; DIAGNOSIS; SERUM; IDENTIFICATION; EPIDEMIOLOGY; INFECTION; MIR-155; MARKERS; GENES;
D O I
10.1038/s41598-020-60132-0
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
Pulmonary disease (PD) due to nontuberculous mycobacteria (NTM) is increasing globally, but specific biomarkers for NTM-PD have not been established. As circulating miRNAs are promising biomarkers for various diseases, we investigated whether miRNAs have potential as NTM-PD biomarkers. Sera from 12 NTM-PD patients due to Mycobacterium avium, M. intracellulare, M. abscessus, or M. massiliense and three healthy controls were initially evaluated via small RNA sequencing. Multiple miRNAs showed significant differences in expression in patients compared to in healthy controls, with some expression differences unique to PD caused by a specific mycobacterial species. Notably, 14 miRNAs exhibited significant expression differences in PD associated with all four mycobacteria. Validation by quantitative reverse-transcription-PCR in an additional 40 patients with NTM-PD and 40 healthy controls confirmed that four differentially expressed miRNAs (hsa-miR-484, hsa-miR-584-5p, hsa-miR-625-3p, and hsa-miR-4732-5p) showed significantly higher serum expressions in NTM-PD patients than in controls. Receiver operating characteristic curve analysis of these four miRNAs supported the discriminative potential for NTM-PD and their combination provided an improved diagnostic value for NTM-PD. Furthermore, bioinformatics analysis revealed their 125 target genes, which were mostly associated with immune responses. Collectively, this study identified four miRNAs as potential biomarkers for NTM-PD and provided insight into NTM-PD pathophysiology.
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页数:13
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