CircRNA0001859, a new diagnostic and prognostic biomarkers for COPD and AECOPD

Background Dysregulation of circRNAs has been reported to be functionally associated with chronic obstructive pulmonary disease (COPD). The present investigation elucidated the potential role of CircRNA0001859 in regulating chronic obstructive pulmonary disease acute (COPD) and Acute Exacerbation of...

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Veröffentlicht in:BMC pulmonary medicine 2020-11, Vol.20 (1), p.1-311, Article 311
Hauptverfasser: Chen, Shuifang, Yao, Yinan, Lu, Shan, Chen, Junjun, Yang, Guangdie, Tu, Lingfang, Chen, Lina
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container_issue 1
container_start_page 1
container_title BMC pulmonary medicine
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creator Chen, Shuifang
Yao, Yinan
Lu, Shan
Chen, Junjun
Yang, Guangdie
Tu, Lingfang
Chen, Lina
description Background Dysregulation of circRNAs has been reported to be functionally associated with chronic obstructive pulmonary disease (COPD). The present investigation elucidated the potential role of CircRNA0001859 in regulating chronic obstructive pulmonary disease acute (COPD) and Acute Exacerbation of COPD (AECOPD). Methods Mice model of COPD was established to screen and verify the dysregulated expression of CircRNA0001859. Fluorescence in situ hybridization (FISH) and quantitative real-time PCR (qRT-PCR) were carried out to detect the expression of CircRNA0001859. 38 stable COPD patients, 24 AECOPD patients, 57 COPD with lung cancer patients and 28 healthy person with age and sex matched to total patients were used for the present investigation. Results circRNA0001859 was downregulated in the lung tissue of mice after the three kinds of treatments (Cigarette smoke (CS)/NK alone or CS + NNK) for inducing COPD. FISH assay verified the downregulation of circRNA0001859 both in the mice lung and human bronchial epithelial cell of COPD model. Furthermore,, the level of circRNA0001859 was also downregulated in the peripheral blood of COPD and lung cancer patients. CircRNA0001859 might act as a diagnostic and prognostic biomarker for the treatment of in COPD and AECOPD with Are under the receiver operating characteristic curve (ROC curve) (AUC) of 0.7433 and 0.8717, respectively. Conclusion We explored a novel circRNA0001859, which might act as a potential therapeutic biomarker for the treatment of COPD and AECOPD. Keywords: Circular RNA0001859 (CircRNA0001859), CS, NNK, Chronic obstructive pulmonary disease (COPD), Acute exacerbation of COPD (AECOPD), Lung cancer
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The present investigation elucidated the potential role of CircRNA0001859 in regulating chronic obstructive pulmonary disease acute (COPD) and Acute Exacerbation of COPD (AECOPD). Methods Mice model of COPD was established to screen and verify the dysregulated expression of CircRNA0001859. Fluorescence in situ hybridization (FISH) and quantitative real-time PCR (qRT-PCR) were carried out to detect the expression of CircRNA0001859. 38 stable COPD patients, 24 AECOPD patients, 57 COPD with lung cancer patients and 28 healthy person with age and sex matched to total patients were used for the present investigation. Results circRNA0001859 was downregulated in the lung tissue of mice after the three kinds of treatments (Cigarette smoke (CS)/NK alone or CS + NNK) for inducing COPD. FISH assay verified the downregulation of circRNA0001859 both in the mice lung and human bronchial epithelial cell of COPD model. Furthermore,, the level of circRNA0001859 was also downregulated in the peripheral blood of COPD and lung cancer patients. CircRNA0001859 might act as a diagnostic and prognostic biomarker for the treatment of in COPD and AECOPD with Are under the receiver operating characteristic curve (ROC curve) (AUC) of 0.7433 and 0.8717, respectively. Conclusion We explored a novel circRNA0001859, which might act as a potential therapeutic biomarker for the treatment of COPD and AECOPD. Keywords: Circular RNA0001859 (CircRNA0001859), CS, NNK, Chronic obstructive pulmonary disease (COPD), Acute exacerbation of COPD (AECOPD), Lung cancer</description><identifier>ISSN: 1471-2466</identifier><identifier>EISSN: 1471-2466</identifier><identifier>DOI: 10.1186/s12890-020-01333-1</identifier><identifier>PMID: 33239003</identifier><language>eng</language><publisher>London: BioMed Central Ltd</publisher><subject>Age ; Autoimmune diseases ; Biological markers ; Biomarkers ; Cell cycle ; Chronic obstructive pulmonary disease ; Cigarette smoke ; Cigarettes ; Coronaviruses ; COVID-19 ; Cytokines ; Diagnosis ; Drug dosages ; Epithelial cells ; Ethics ; Fluorescence in situ hybridization ; Genetic aspects ; Health aspects ; Humidity ; Hypertension ; Infections ; Lavage ; Lung cancer ; Lung diseases ; Lung diseases, Obstructive ; Medical research ; Obstructive lung disease ; Peripheral blood ; Pulmonary arteries ; Pulmonology ; RNA ; Tuberculosis ; Tumor necrosis factor-TNF</subject><ispartof>BMC pulmonary medicine, 2020-11, Vol.20 (1), p.1-311, Article 311</ispartof><rights>COPYRIGHT 2020 BioMed Central Ltd.</rights><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-9653c126c03f0ce10424daf4ebbe648f91c49c1e492666f97838a92152ca94b73</citedby><cites>FETCH-LOGICAL-c474t-9653c126c03f0ce10424daf4ebbe648f91c49c1e492666f97838a92152ca94b73</cites><orcidid>0000-0001-8463-0365</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688204/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688204/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Chen, Shuifang</creatorcontrib><creatorcontrib>Yao, Yinan</creatorcontrib><creatorcontrib>Lu, Shan</creatorcontrib><creatorcontrib>Chen, Junjun</creatorcontrib><creatorcontrib>Yang, Guangdie</creatorcontrib><creatorcontrib>Tu, Lingfang</creatorcontrib><creatorcontrib>Chen, Lina</creatorcontrib><title>CircRNA0001859, a new diagnostic and prognostic biomarkers for COPD and AECOPD</title><title>BMC pulmonary medicine</title><description>Background Dysregulation of circRNAs has been reported to be functionally associated with chronic obstructive pulmonary disease (COPD). The present investigation elucidated the potential role of CircRNA0001859 in regulating chronic obstructive pulmonary disease acute (COPD) and Acute Exacerbation of COPD (AECOPD). Methods Mice model of COPD was established to screen and verify the dysregulated expression of CircRNA0001859. Fluorescence in situ hybridization (FISH) and quantitative real-time PCR (qRT-PCR) were carried out to detect the expression of CircRNA0001859. 38 stable COPD patients, 24 AECOPD patients, 57 COPD with lung cancer patients and 28 healthy person with age and sex matched to total patients were used for the present investigation. Results circRNA0001859 was downregulated in the lung tissue of mice after the three kinds of treatments (Cigarette smoke (CS)/NK alone or CS + NNK) for inducing COPD. FISH assay verified the downregulation of circRNA0001859 both in the mice lung and human bronchial epithelial cell of COPD model. Furthermore,, the level of circRNA0001859 was also downregulated in the peripheral blood of COPD and lung cancer patients. CircRNA0001859 might act as a diagnostic and prognostic biomarker for the treatment of in COPD and AECOPD with Are under the receiver operating characteristic curve (ROC curve) (AUC) of 0.7433 and 0.8717, respectively. Conclusion We explored a novel circRNA0001859, which might act as a potential therapeutic biomarker for the treatment of COPD and AECOPD. 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The present investigation elucidated the potential role of CircRNA0001859 in regulating chronic obstructive pulmonary disease acute (COPD) and Acute Exacerbation of COPD (AECOPD). Methods Mice model of COPD was established to screen and verify the dysregulated expression of CircRNA0001859. Fluorescence in situ hybridization (FISH) and quantitative real-time PCR (qRT-PCR) were carried out to detect the expression of CircRNA0001859. 38 stable COPD patients, 24 AECOPD patients, 57 COPD with lung cancer patients and 28 healthy person with age and sex matched to total patients were used for the present investigation. Results circRNA0001859 was downregulated in the lung tissue of mice after the three kinds of treatments (Cigarette smoke (CS)/NK alone or CS + NNK) for inducing COPD. FISH assay verified the downregulation of circRNA0001859 both in the mice lung and human bronchial epithelial cell of COPD model. Furthermore,, the level of circRNA0001859 was also downregulated in the peripheral blood of COPD and lung cancer patients. CircRNA0001859 might act as a diagnostic and prognostic biomarker for the treatment of in COPD and AECOPD with Are under the receiver operating characteristic curve (ROC curve) (AUC) of 0.7433 and 0.8717, respectively. Conclusion We explored a novel circRNA0001859, which might act as a potential therapeutic biomarker for the treatment of COPD and AECOPD. Keywords: Circular RNA0001859 (CircRNA0001859), CS, NNK, Chronic obstructive pulmonary disease (COPD), Acute exacerbation of COPD (AECOPD), Lung cancer</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><pmid>33239003</pmid><doi>10.1186/s12890-020-01333-1</doi><orcidid>https://orcid.org/0000-0001-8463-0365</orcidid><oa>free_for_read</oa></addata></record>
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subjects Age
Autoimmune diseases
Biological markers
Biomarkers
Cell cycle
Chronic obstructive pulmonary disease
Cigarette smoke
Cigarettes
Coronaviruses
COVID-19
Cytokines
Diagnosis
Drug dosages
Epithelial cells
Ethics
Fluorescence in situ hybridization
Genetic aspects
Health aspects
Humidity
Hypertension
Infections
Lavage
Lung cancer
Lung diseases
Lung diseases, Obstructive
Medical research
Obstructive lung disease
Peripheral blood
Pulmonary arteries
Pulmonology
RNA
Tuberculosis
Tumor necrosis factor-TNF
title CircRNA0001859, a new diagnostic and prognostic biomarkers for COPD and AECOPD
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