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Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin

Purpose. The interaction of hormones of the pituitary-adrenal axis and adrenal cortex-associated circulating microRNAs is mostly unknown. We have studied the effects of dexamethasone and adrenocorticotropin on the expression of five circulating microRNAs (hsa-miR-27a, hsa-miR-200b, hsa-miR-214, hsa-...

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Autores principales: Igaz, Ivan, Nyírő, Gábor, Nagy, Zoltán, Butz, Henriett, Nagy, Zsolt, Perge, Pál, Sahin, Peter, Tóth, Miklós, Rácz, Károly, Igaz, Peter, Patócs, Attila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487905/
https://www.ncbi.nlm.nih.gov/pubmed/26161091
http://dx.doi.org/10.1155/2015/589230
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author Igaz, Ivan
Nyírő, Gábor
Nagy, Zoltán
Butz, Henriett
Nagy, Zsolt
Perge, Pál
Sahin, Peter
Tóth, Miklós
Rácz, Károly
Igaz, Peter
Patócs, Attila
author_facet Igaz, Ivan
Nyírő, Gábor
Nagy, Zoltán
Butz, Henriett
Nagy, Zsolt
Perge, Pál
Sahin, Peter
Tóth, Miklós
Rácz, Károly
Igaz, Peter
Patócs, Attila
author_sort Igaz, Ivan
collection PubMed
description Purpose. The interaction of hormones of the pituitary-adrenal axis and adrenal cortex-associated circulating microRNAs is mostly unknown. We have studied the effects of dexamethasone and adrenocorticotropin on the expression of five circulating microRNAs (hsa-miR-27a, hsa-miR-200b, hsa-miR-214, hsa-miR-483-5p, and hsa-miR-503) reported to be related to the adrenal cortex in plasma samples. Methods. Expression of microRNAs was studied in plasma samples of 10 individuals examined by 1 mg dexamethasone suppression test and another 10 individuals stimulated by 250 μg tetracosactide (adrenocorticotropin). Total RNA was isolated and microRNA expression was analyzed by real-time reverse transcription quantitative polymerase chain reaction normalized to cel-miR-39 as reference. Results. Only circulating hsa-miR-27a proved to be significantly modulated in vivo by hormonal treatments: its expression was upregulated by dexamethasone whereas it was suppressed by adrenocorticotropin. Secreted hsa-miR-27a was significantly induced by dexamethasone in vitro in NCI-H295R cells, as well. The expression of hsa-miR-483-5p proposed as diagnostic marker for adrenocortical malignancy was not affected by dexamethasone or tetracosactide administration. Conclusions. hsa-miR-27a expression is modulated by hormones of the hypothalamic-pituitary-adrenal axis both in vitro and in vivo. The biological relevance of hsa-miR-27a modulation by hormones is unclear, but the responsiveness of circulating microRNAs to hormones of the pituitary-adrenal axis is noteworthy.
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spelling pubmed-44879052015-07-09 Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin Igaz, Ivan Nyírő, Gábor Nagy, Zoltán Butz, Henriett Nagy, Zsolt Perge, Pál Sahin, Peter Tóth, Miklós Rácz, Károly Igaz, Peter Patócs, Attila Int J Endocrinol Clinical Study Purpose. The interaction of hormones of the pituitary-adrenal axis and adrenal cortex-associated circulating microRNAs is mostly unknown. We have studied the effects of dexamethasone and adrenocorticotropin on the expression of five circulating microRNAs (hsa-miR-27a, hsa-miR-200b, hsa-miR-214, hsa-miR-483-5p, and hsa-miR-503) reported to be related to the adrenal cortex in plasma samples. Methods. Expression of microRNAs was studied in plasma samples of 10 individuals examined by 1 mg dexamethasone suppression test and another 10 individuals stimulated by 250 μg tetracosactide (adrenocorticotropin). Total RNA was isolated and microRNA expression was analyzed by real-time reverse transcription quantitative polymerase chain reaction normalized to cel-miR-39 as reference. Results. Only circulating hsa-miR-27a proved to be significantly modulated in vivo by hormonal treatments: its expression was upregulated by dexamethasone whereas it was suppressed by adrenocorticotropin. Secreted hsa-miR-27a was significantly induced by dexamethasone in vitro in NCI-H295R cells, as well. The expression of hsa-miR-483-5p proposed as diagnostic marker for adrenocortical malignancy was not affected by dexamethasone or tetracosactide administration. Conclusions. hsa-miR-27a expression is modulated by hormones of the hypothalamic-pituitary-adrenal axis both in vitro and in vivo. The biological relevance of hsa-miR-27a modulation by hormones is unclear, but the responsiveness of circulating microRNAs to hormones of the pituitary-adrenal axis is noteworthy. Hindawi Publishing Corporation 2015 2015-06-16 /pmc/articles/PMC4487905/ /pubmed/26161091 http://dx.doi.org/10.1155/2015/589230 Text en Copyright © 2015 Ivan Igaz et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Igaz, Ivan
Nyírő, Gábor
Nagy, Zoltán
Butz, Henriett
Nagy, Zsolt
Perge, Pál
Sahin, Peter
Tóth, Miklós
Rácz, Károly
Igaz, Peter
Patócs, Attila
Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
title Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
title_full Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
title_fullStr Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
title_full_unstemmed Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
title_short Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin
title_sort analysis of circulating micrornas in vivo following administration of dexamethasone and adrenocorticotropin
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487905/
https://www.ncbi.nlm.nih.gov/pubmed/26161091
http://dx.doi.org/10.1155/2015/589230
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