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Circular RNA profiles in mouse lung tissue induced by radon
BACKGROUND: Radon is a known human lung carcinogen, whose underlying carcinogenic mechanism remains unclear. Recently, circular RNA (circRNA), a class of endogenous non-protein coding RNAs that contain a circular loop, was found to exhibit multiple biological effects. In this study, circRNA profiles...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664590/ https://www.ncbi.nlm.nih.gov/pubmed/29165116 http://dx.doi.org/10.1186/s12199-017-0627-6 |
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author | Pei, Weiwei Tao, Lijing Zhang, Leshuai W. Zhang, Shuyu Cao, Jianping Jiao, Yang Tong, Jian Nie, Jihua |
author_facet | Pei, Weiwei Tao, Lijing Zhang, Leshuai W. Zhang, Shuyu Cao, Jianping Jiao, Yang Tong, Jian Nie, Jihua |
author_sort | Pei, Weiwei |
collection | PubMed |
description | BACKGROUND: Radon is a known human lung carcinogen, whose underlying carcinogenic mechanism remains unclear. Recently, circular RNA (circRNA), a class of endogenous non-protein coding RNAs that contain a circular loop, was found to exhibit multiple biological effects. In this study, circRNA profiles in mouse lung tissues between control and radon exposure were analyzed. METHODS: Six mice were exposed to radon at concentration of 100,000 Bq/m(3), 12 h/d, for up to cumulative doses of 60 working level months (WLM). H&E staining and immunohistochemistry of caspase-3 were used to detect the damages in lung tissue. The lung tissue of control and exposed group were selected for circRNA microarray study. The circRNA/microRNA interaction was analyzed by starBase prediction software. 5 highest expressing circRNAs were selected by real-time PCR to validate the consistency in mouse lung tissue exposed to radon. RESULTS: Inflammatory reaction was found in mouse lung tissue exposed to radon, and caspase-3 expression was significantly increased. Microarray screening revealed 107 up-regulated and 83 down-regulated circRNAs, among which top 30 circRNAs with the highest fold changes were chosen for further analysis, with 5 microRNAs binding sites listed for each circRNA. Consistency of the top 5 circRNAs with the highest expressions were confirmed in mice exposed with 60WLM of radon. CONCLUSION: Mouse lung tissue was severely injured when exposed to radon through pathological diagnosis and immunohistochemical analysis. A series of differentially expressed circRNAs demonstrated that they may play an important role in pulmonary toxicity induced by radon. |
format | Online Article Text |
id | pubmed-5664590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56645902017-11-08 Circular RNA profiles in mouse lung tissue induced by radon Pei, Weiwei Tao, Lijing Zhang, Leshuai W. Zhang, Shuyu Cao, Jianping Jiao, Yang Tong, Jian Nie, Jihua Environ Health Prev Med Research Article BACKGROUND: Radon is a known human lung carcinogen, whose underlying carcinogenic mechanism remains unclear. Recently, circular RNA (circRNA), a class of endogenous non-protein coding RNAs that contain a circular loop, was found to exhibit multiple biological effects. In this study, circRNA profiles in mouse lung tissues between control and radon exposure were analyzed. METHODS: Six mice were exposed to radon at concentration of 100,000 Bq/m(3), 12 h/d, for up to cumulative doses of 60 working level months (WLM). H&E staining and immunohistochemistry of caspase-3 were used to detect the damages in lung tissue. The lung tissue of control and exposed group were selected for circRNA microarray study. The circRNA/microRNA interaction was analyzed by starBase prediction software. 5 highest expressing circRNAs were selected by real-time PCR to validate the consistency in mouse lung tissue exposed to radon. RESULTS: Inflammatory reaction was found in mouse lung tissue exposed to radon, and caspase-3 expression was significantly increased. Microarray screening revealed 107 up-regulated and 83 down-regulated circRNAs, among which top 30 circRNAs with the highest fold changes were chosen for further analysis, with 5 microRNAs binding sites listed for each circRNA. Consistency of the top 5 circRNAs with the highest expressions were confirmed in mice exposed with 60WLM of radon. CONCLUSION: Mouse lung tissue was severely injured when exposed to radon through pathological diagnosis and immunohistochemical analysis. A series of differentially expressed circRNAs demonstrated that they may play an important role in pulmonary toxicity induced by radon. BioMed Central 2017-04-07 2017 /pmc/articles/PMC5664590/ /pubmed/29165116 http://dx.doi.org/10.1186/s12199-017-0627-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pei, Weiwei Tao, Lijing Zhang, Leshuai W. Zhang, Shuyu Cao, Jianping Jiao, Yang Tong, Jian Nie, Jihua Circular RNA profiles in mouse lung tissue induced by radon |
title | Circular RNA profiles in mouse lung tissue induced by radon |
title_full | Circular RNA profiles in mouse lung tissue induced by radon |
title_fullStr | Circular RNA profiles in mouse lung tissue induced by radon |
title_full_unstemmed | Circular RNA profiles in mouse lung tissue induced by radon |
title_short | Circular RNA profiles in mouse lung tissue induced by radon |
title_sort | circular rna profiles in mouse lung tissue induced by radon |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664590/ https://www.ncbi.nlm.nih.gov/pubmed/29165116 http://dx.doi.org/10.1186/s12199-017-0627-6 |
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