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MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions

Studies in the cardiovascular research field have demonstrated the vital roles of microRNAs for proper cardiovascular development and functional maintenance. The involvement of aberrant microRNA expression leading to ontogenesis of cardiovascular diseases lends further support of the regulatory role...

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Autores principales: Chen, Yei-Tsung, Liew, Oi-Wah, Richards, Arthur Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583634/
https://www.ncbi.nlm.nih.gov/pubmed/26484225
http://dx.doi.org/10.1016/j.gdata.2015.05.020
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author Chen, Yei-Tsung
Liew, Oi-Wah
Richards, Arthur Mark
author_facet Chen, Yei-Tsung
Liew, Oi-Wah
Richards, Arthur Mark
author_sort Chen, Yei-Tsung
collection PubMed
description Studies in the cardiovascular research field have demonstrated the vital roles of microRNAs for proper cardiovascular development and functional maintenance. The involvement of aberrant microRNA expression leading to ontogenesis of cardiovascular diseases lends further support of the regulatory role of microRNAs in heart function. Hypoxic insult is one of the major factors that trigger downstream signal cascades which contribute to the pathogenesis of hypoxic/ischemic-related heart diseases. Here, we report the microRNA expression profile in human cardiac-derived cells subjected to 120-h hypoxic treatment. By comparing with the normoxic control state, we identified microRNAs differentially expressed in cardiac cells subjected to hypoxic challenge. MicroRNA microarray data are available at NCBI under the GEO accession number, GSE55387.
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spelling pubmed-45836342015-10-19 MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions Chen, Yei-Tsung Liew, Oi-Wah Richards, Arthur Mark Genom Data Data in Brief Studies in the cardiovascular research field have demonstrated the vital roles of microRNAs for proper cardiovascular development and functional maintenance. The involvement of aberrant microRNA expression leading to ontogenesis of cardiovascular diseases lends further support of the regulatory role of microRNAs in heart function. Hypoxic insult is one of the major factors that trigger downstream signal cascades which contribute to the pathogenesis of hypoxic/ischemic-related heart diseases. Here, we report the microRNA expression profile in human cardiac-derived cells subjected to 120-h hypoxic treatment. By comparing with the normoxic control state, we identified microRNAs differentially expressed in cardiac cells subjected to hypoxic challenge. MicroRNA microarray data are available at NCBI under the GEO accession number, GSE55387. Elsevier 2015-05-29 /pmc/articles/PMC4583634/ /pubmed/26484225 http://dx.doi.org/10.1016/j.gdata.2015.05.020 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Data in Brief
Chen, Yei-Tsung
Liew, Oi-Wah
Richards, Arthur Mark
MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
title MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
title_full MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
title_fullStr MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
title_full_unstemmed MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
title_short MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
title_sort microrna expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions
topic Data in Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583634/
https://www.ncbi.nlm.nih.gov/pubmed/26484225
http://dx.doi.org/10.1016/j.gdata.2015.05.020
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