Literature DB >> 23338559

Clinical relevance of plasma miR-106b levels in patients with chronic obstructive pulmonary disease.

Seiko Soeda1, Junko H Ohyashiki, Kazushige Ohtsuki, Tomohiro Umezu, Yasuhiro Setoguchi, Kazuma Ohyashiki.   

Abstract

Chronic obstructive pulmonary disease (COPD) is characterized by both chronic inflammation in the airway and systemic inflammation; however, the molecular mechanism of COPD has not been fully elucidated. By measuring microRNA (miRNA) expression in the plasma of COPD subjects, we aimed to identify the clinical relevance of plasma miRNA levels in these patients. Blood samples were obtained from COPD patients and age-matched normal controls. We initially produced plasma miRNA expression profiles using TaqMan low-density array screening. For further validation, individual qRT-PCRs were performed in 40 COPD patients and 20 healthy subjects. TaqMan low-density array screening showed that 9 miRNAs (miR-29b, miR-483-5p, miR-152, miR-629, miR-26b, miR-101, miR-106b, miR-532-5p and miR-133b) were significantly downregulated in the plasma from COPD patients when compared with normal smokers. Among these miRNAs, we focused on miR-106b. A reduction in the plasma miR-106b levels was evident in COPD ex-smokers and COPD current smokers compared with levels in smokers. There was a negative correlation between the plasma miR-106b level and the duration of disease since diagnosis in COPD ex-smokers and the duration of smoking in COPD current smokers. These findings support the concept that progressive reduction in the plasma miR-106b level may reflect persistent and systemic changes even after the discontinuation of smoking in COPD patients. miR-106b may therefore play an important role in the pathogenesis of COPD.

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Year:  2013        PMID: 23338559     DOI: 10.3892/ijmm.2013.1251

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  24 in total

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2.  Downregulated miR-486-5p acts as a tumor suppressor in esophageal squamous cell carcinoma.

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Authors:  Zuhu Yu; Liangchao Ni; Duqun Chen; Qiang Zhang; Zhengming Su; Yadong Wang; Wenshui Yu; Xionghui Wu; Jiongxian Ye; Shangqi Yang; Yongqing Lai; Xianxin Li
Journal:  J Mol Histol       Date:  2013-06-21       Impact factor: 2.611

Review 4.  Epigenetic targets for novel therapies of lung diseases.

Authors:  Brian S Comer; Mariam Ba; Cherie A Singer; William T Gerthoffer
Journal:  Pharmacol Ther       Date:  2014-11-15       Impact factor: 12.310

5.  Identification of common microRNA between COPD and non-small cell lung cancer through pathway enrichment analysis.

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Journal:  BMC Genom Data       Date:  2021-10-12

6.  Assay reproducibility in clinical studies of plasma miRNA.

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Journal:  PLoS One       Date:  2015-04-08       Impact factor: 3.240

Review 7.  Novel insights into miRNA in lung and heart inflammatory diseases.

Authors:  Amit Kishore; Jana Borucka; Jana Petrkova; Martin Petrek
Journal:  Mediators Inflamm       Date:  2014-05-27       Impact factor: 4.711

8.  MicroRNA-532 protects the heart in acute myocardial infarction, and represses prss23, a positive regulator of endothelial-to-mesenchymal transition.

Authors:  Ahmed S Bayoumi; Jian-Peng Teoh; Tatsuya Aonuma; Zhize Yuan; Xiaofen Ruan; Yaoliang Tang; Huabo Su; Neal L Weintraub; Il-Man Kim
Journal:  Cardiovasc Res       Date:  2017-11-01       Impact factor: 10.787

9.  Plasma Extracellular Vesicle miRNAs Can Identify Lung Cancer, Current Smoking Status, and Stable COPD.

Authors:  Hannah E O'Farrell; Rayleen V Bowman; Kwun M Fong; Ian A Yang
Journal:  Int J Mol Sci       Date:  2021-05-28       Impact factor: 5.923

Review 10.  Methodological challenges in utilizing miRNAs as circulating biomarkers.

Authors:  Leni Moldovan; Kara E Batte; Joanne Trgovcich; Jon Wisler; Clay B Marsh; Melissa Piper
Journal:  J Cell Mol Med       Date:  2014-02-18       Impact factor: 5.310

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