Analysis of serum micro-RNAs as potential biomarker in chronic obstructive pulmonary disease

被引:102
作者
Akbas, Fahri [1 ]
Coskunpinar, Ender [2 ]
Aynaci, Engin [3 ]
Oltulu, Yasemin Musteri [2 ]
Yildiz, Pinar [3 ]
机构
[1] Fatih Univ, Dept Genet & Bioengn, TR-34500 Istanbul, Turkey
[2] Istanbul Univ, Inst Expt Med, Dept Mol Med, Istanbul, Turkey
[3] Yedikule Chest Dis & Chest Surg Training & Res Ho, Istanbul, Turkey
关键词
gene expression; molecular marker; quantitative RT-PCR; GROWTH-FACTOR RECEPTOR; DOWN-REGULATION; CIRCULATING MICRORNAS; GENETIC-VARIANTS; LUNG-DISEASE; EXPRESSION; CANCER; RISK; ASSOCIATION; ACTIVATION;
D O I
10.3109/01902148.2012.689088
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Chronic obstructive pulmonary disease (COPD) as a complex disease with genetic and environmental compound is one of the leading causes of death in worldwide. This disease is characterized by lower airway inflammation, and increases risk of lung cancer in smokers. Micro-RNA (miRNA) molecules are key regulators in gene expression that have been widely associated with a several diseases. Differential expression of miRNAs is involved in lung tissue of COPD, but there is no information about biomarker potential of circulating miRNAs in patients. To analyze the miRNA expression profile in COPD, levels of serum miRNAs were profiled by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) array system. The authors examined 72 miRNAs by qRT-PCR array, in 20 COPD patients and 12 control subjects. U6snRNA was used for normalization of the expression of miRNAs for each sample. According to the results, 5 miRNAs were found to be significantly dysregulated. There was down-regulation of miR-20a, miR-28-3p, miR-34c-5p, and miR-100, and up-regulation of miR-7, compared with the controls. This was the first study in COPD for screening of serum miRNAs for searching for biomarker. These results are preliminary screening data and should be confirmed with large patient groups. If so, these miRNAs are likely being involved in pathogenesis of COPD and may give clues for designing therapeutic strategy.
引用
收藏
页码:286 / 294
页数:9
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