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Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas
The abnormal expression of microRNAs (miRNAs) is implicated in various human diseases, including cancers. Accordingly, miRNA expressions have been examined in many cancer tissues and blood, but there have been few studies examining smear samples from bone marrow (BM) or peripheral blood. Here we suc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072855/ https://www.ncbi.nlm.nih.gov/pubmed/25019040 http://dx.doi.org/10.1186/2193-1801-3-288 |
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author | Takei, Yoshifumi Ohnishi, Naomi Kisaka, Mayumi Mihara, Keichiro |
author_facet | Takei, Yoshifumi Ohnishi, Naomi Kisaka, Mayumi Mihara, Keichiro |
author_sort | Takei, Yoshifumi |
collection | PubMed |
description | The abnormal expression of microRNAs (miRNAs) is implicated in various human diseases, including cancers. Accordingly, miRNA expressions have been examined in many cancer tissues and blood, but there have been few studies examining smear samples from bone marrow (BM) or peripheral blood. Here we successfully isolated small RNAs from BM smears using a mirVana miRNA Isolation Kit with our original modifications. The isolated small RNAs were then used to measure the levels of representative miRNAs such as miR-155, let-7a, and U6 via real-time PCR with a specific TaqMan probe, although peaks for the ribosomal RNAs (18S, and 28S) were not identified. The PCR curves of the miRNAs were indistinguishable from those from BM living cells from the same donor. Finally, our method for BM smears identified numerous abnormally altered miRNAs (significantly decreased, 39 miRNAs; significantly increased, 27 miRNAs) in follicular lymphomas (FL) compared with normal donors via TaqMan real-time PCR miRNA array. The array indicated that miR-451 showed the greatest decrease in FL (a 345-fold decrease), while miR-338-5p showed the greatest increase in FL (172-fold) relative to normal donors. The miRNAs identified by our study might serve as markers to predict the invasion of FL cells into BM without biopsy. Furthermore, our method will provide a new avenue for the analysis of miRNAs in BM smear samples from various hematologic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi: 10.1186/2193-1801-3-288) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4072855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-40728552014-07-11 Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas Takei, Yoshifumi Ohnishi, Naomi Kisaka, Mayumi Mihara, Keichiro Springerplus Research The abnormal expression of microRNAs (miRNAs) is implicated in various human diseases, including cancers. Accordingly, miRNA expressions have been examined in many cancer tissues and blood, but there have been few studies examining smear samples from bone marrow (BM) or peripheral blood. Here we successfully isolated small RNAs from BM smears using a mirVana miRNA Isolation Kit with our original modifications. The isolated small RNAs were then used to measure the levels of representative miRNAs such as miR-155, let-7a, and U6 via real-time PCR with a specific TaqMan probe, although peaks for the ribosomal RNAs (18S, and 28S) were not identified. The PCR curves of the miRNAs were indistinguishable from those from BM living cells from the same donor. Finally, our method for BM smears identified numerous abnormally altered miRNAs (significantly decreased, 39 miRNAs; significantly increased, 27 miRNAs) in follicular lymphomas (FL) compared with normal donors via TaqMan real-time PCR miRNA array. The array indicated that miR-451 showed the greatest decrease in FL (a 345-fold decrease), while miR-338-5p showed the greatest increase in FL (172-fold) relative to normal donors. The miRNAs identified by our study might serve as markers to predict the invasion of FL cells into BM without biopsy. Furthermore, our method will provide a new avenue for the analysis of miRNAs in BM smear samples from various hematologic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi: 10.1186/2193-1801-3-288) contains supplementary material, which is available to authorized users. Springer International Publishing 2014-06-07 /pmc/articles/PMC4072855/ /pubmed/25019040 http://dx.doi.org/10.1186/2193-1801-3-288 Text en © Takei et al.; licensee Springer. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Takei, Yoshifumi Ohnishi, Naomi Kisaka, Mayumi Mihara, Keichiro Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas |
title | Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas |
title_full | Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas |
title_fullStr | Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas |
title_full_unstemmed | Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas |
title_short | Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas |
title_sort | determination of abnormally expressed micrornas in bone marrow smears from patients with follicular lymphomas |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072855/ https://www.ncbi.nlm.nih.gov/pubmed/25019040 http://dx.doi.org/10.1186/2193-1801-3-288 |
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