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Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies?
MicroRNAs (miRNAs) are differentially expressed in the brain under pathologic conditions and may therefore represent both therapeutic targets and diagnostic or prognostic biomarkers for neurologic diseases, including epilepsy. In fact, miRNA expression profiles have been investigated in the hippocam...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939384/ https://www.ncbi.nlm.nih.gov/pubmed/29750217 http://dx.doi.org/10.1002/epi4.12023 |
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author | Roncon, Paolo Zucchini, Silvia Ferracin, Manuela Marucci, Gianluca Giulioni, Marco Michelucci, Roberto Rubboli, Guido Simonato, Michele |
author_facet | Roncon, Paolo Zucchini, Silvia Ferracin, Manuela Marucci, Gianluca Giulioni, Marco Michelucci, Roberto Rubboli, Guido Simonato, Michele |
author_sort | Roncon, Paolo |
collection | PubMed |
description | MicroRNAs (miRNAs) are differentially expressed in the brain under pathologic conditions and may therefore represent both therapeutic targets and diagnostic or prognostic biomarkers for neurologic diseases, including epilepsy. In fact, miRNA expression profiles have been investigated in the hippocampi of patients with epilepsy in comparison with control, nonepileptic cases. Unfortunately, the interpretation of these data is difficult because surgically resected epileptic tissue is generally compared with control tissue obtained from autopsies. To challenge the validity of this approach, we performed an miRNA microarray on the laser microdissected granule cell layer of the human hippocampus obtained from surgical samples of patients with epilepsy, autoptic nonepileptic controls, and patients with autoptic epilepsy, using the latter as internal control. Unfortunately, it is extremely difficult to collect autopsy material from documented epilepsy individuals who died of non–epilepsy‐related causes—we found only two such cases. However, hierarchical clustering of all samples showed that those obtained from autopsies of patients with epilepsy segregated with the other autoptic samples (controls) and not with the bioptic tissues from the surgery patients, suggesting that the origin of the tissue (surgery or autopsy) may be prevalent over the underlying pathology (epilepsy or not epilepsy). Even taking into account the limitations due to the small number of cases, this observation arises concerns on the use of autopsy tissue as control for this kind of studies. |
format | Online Article Text |
id | pubmed-5939384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59393842018-05-10 Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? Roncon, Paolo Zucchini, Silvia Ferracin, Manuela Marucci, Gianluca Giulioni, Marco Michelucci, Roberto Rubboli, Guido Simonato, Michele Epilepsia Open Short Research Articles MicroRNAs (miRNAs) are differentially expressed in the brain under pathologic conditions and may therefore represent both therapeutic targets and diagnostic or prognostic biomarkers for neurologic diseases, including epilepsy. In fact, miRNA expression profiles have been investigated in the hippocampi of patients with epilepsy in comparison with control, nonepileptic cases. Unfortunately, the interpretation of these data is difficult because surgically resected epileptic tissue is generally compared with control tissue obtained from autopsies. To challenge the validity of this approach, we performed an miRNA microarray on the laser microdissected granule cell layer of the human hippocampus obtained from surgical samples of patients with epilepsy, autoptic nonepileptic controls, and patients with autoptic epilepsy, using the latter as internal control. Unfortunately, it is extremely difficult to collect autopsy material from documented epilepsy individuals who died of non–epilepsy‐related causes—we found only two such cases. However, hierarchical clustering of all samples showed that those obtained from autopsies of patients with epilepsy segregated with the other autoptic samples (controls) and not with the bioptic tissues from the surgery patients, suggesting that the origin of the tissue (surgery or autopsy) may be prevalent over the underlying pathology (epilepsy or not epilepsy). Even taking into account the limitations due to the small number of cases, this observation arises concerns on the use of autopsy tissue as control for this kind of studies. John Wiley and Sons Inc. 2016-11-09 /pmc/articles/PMC5939384/ /pubmed/29750217 http://dx.doi.org/10.1002/epi4.12023 Text en © 2016 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Research Articles Roncon, Paolo Zucchini, Silvia Ferracin, Manuela Marucci, Gianluca Giulioni, Marco Michelucci, Roberto Rubboli, Guido Simonato, Michele Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? |
title | Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? |
title_full | Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? |
title_fullStr | Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? |
title_full_unstemmed | Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? |
title_short | Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? |
title_sort | is autopsy tissue a valid control for epilepsy surgery tissue in microrna studies? |
topic | Short Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939384/ https://www.ncbi.nlm.nih.gov/pubmed/29750217 http://dx.doi.org/10.1002/epi4.12023 |
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