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pmid:26484225

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

Yei-Tsung Chen · Oi-Wah Liew · Arthur Mark Richards

Genomics data · 2015 doi:10.1016/j.gdata.2015.05.020

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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MicroRNA expression profiles of human left ventricle derived cardiac cells in normoxic and hypoxic conditions.
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10.1016/j.gdata.2015.05.020
pmid
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Yei-Tsung Chen
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Oi-Wah Liew
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Arthur Mark Richards
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Genomics data
year
2015
abstract
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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Student's t-test was applied to compare the difference of 4 signal intensity readouts for individual microRNAs between experimental groups (normoxia vs. hypoxia), and microRNAs with significant difference between experimental groups (p < 0.05) were included for further analysis.
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Student's t-test was applied to compare the difference of 4 signal intensity readouts for individual microRNAs between experimental groups (normoxia vs. hypoxia), and microRNAs with significant difference between experimental groups (p < 0.05) were included for further analysis.
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Human cardiac-derived cells subjected to 120-h hypoxic treatment showed differentially expressed microRNAs compared with normoxic controls; the source microarray data are available through GEO accession GSE55387.
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By comparing with the normoxic control state, we identified microRNAs differentially expressed in cardiac cells subjected to hypoxic challenge.
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Human cardiac-derived cells subjected to 120-h hypoxic treatment showed differentially expressed microRNAs compared with normoxic controls; the source microarray data are available through GEO accession GSE55387.
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Natriuretic Peptide Receptor 3 (NPR3) is regulated by microRNA-100
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