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Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells
Certain microRNAs (miRNAs) targeting the molecules in the insulin signaling cascades are dysregulated by saturated fatty acids (SFA), which can lead to insulin resistance and type 2 diabetes. This article reports the accompanying data collected using miRNAs microarrays to identify the changes in miR...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123059/ https://www.ncbi.nlm.nih.gov/pubmed/27900351 http://dx.doi.org/10.1016/j.dib.2016.11.062 |
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author | Yang, Won-Mo Min, Kyung-Ho Lee, Wan |
author_facet | Yang, Won-Mo Min, Kyung-Ho Lee, Wan |
author_sort | Yang, Won-Mo |
collection | PubMed |
description | Certain microRNAs (miRNAs) targeting the molecules in the insulin signaling cascades are dysregulated by saturated fatty acids (SFA), which can lead to insulin resistance and type 2 diabetes. This article reports the accompanying data collected using miRNAs microarrays to identify the changes in miRNA expression in HepG2 cells treated with SFA palmitate. Differentially expressed miRNA analyses in HepG2 cells showed that a range of upregulated (>1.5-fold) or downregulated (<0.5-fold) miRNAs. Further extensive insights into the implications of miRNAs, particularly miR-1271, in HepG2 cells can be found in "MiR-1271 upregulated by saturated fatty acid palmitate provokes impaired insulin signaling by repressing INSR and IRS-1 expression in HepG2 cells" (W.M. Yang, K.H. Min, W. Lee, 2016) [1]. |
format | Online Article Text |
id | pubmed-5123059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-51230592016-11-29 Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells Yang, Won-Mo Min, Kyung-Ho Lee, Wan Data Brief Data Article Certain microRNAs (miRNAs) targeting the molecules in the insulin signaling cascades are dysregulated by saturated fatty acids (SFA), which can lead to insulin resistance and type 2 diabetes. This article reports the accompanying data collected using miRNAs microarrays to identify the changes in miRNA expression in HepG2 cells treated with SFA palmitate. Differentially expressed miRNA analyses in HepG2 cells showed that a range of upregulated (>1.5-fold) or downregulated (<0.5-fold) miRNAs. Further extensive insights into the implications of miRNAs, particularly miR-1271, in HepG2 cells can be found in "MiR-1271 upregulated by saturated fatty acid palmitate provokes impaired insulin signaling by repressing INSR and IRS-1 expression in HepG2 cells" (W.M. Yang, K.H. Min, W. Lee, 2016) [1]. Elsevier 2016-11-19 /pmc/articles/PMC5123059/ /pubmed/27900351 http://dx.doi.org/10.1016/j.dib.2016.11.062 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Data Article Yang, Won-Mo Min, Kyung-Ho Lee, Wan Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells |
title | Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells |
title_full | Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells |
title_fullStr | Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells |
title_full_unstemmed | Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells |
title_short | Data for differentially expressed microRNAs in saturated fatty acid palmitate-treated HepG2 cells |
title_sort | data for differentially expressed micrornas in saturated fatty acid palmitate-treated hepg2 cells |
topic | Data Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123059/ https://www.ncbi.nlm.nih.gov/pubmed/27900351 http://dx.doi.org/10.1016/j.dib.2016.11.062 |
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