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Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia
Recently it was reported that microRNA from the miR-17 ~ 92 family may have a key role in chronic lymphocytic leukemia (CLL). Here, we designed specific oligonucleotides to target endogenous miR-17 (antagomiR17). In-vitro administration of antagomiR17 effectively reduced miR-17 expression and the pr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210490/ https://www.ncbi.nlm.nih.gov/pubmed/25339346 http://dx.doi.org/10.1186/s13045-014-0079-z |
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author | Dereani, Sara Macor, Paolo D’Agaro, Tiziana Mezzaroba, Nelly Dal-Bo, Michele Capolla, Sara Zucchetto, Antonella Tissino, Erika Del Poeta, Giovanni Zorzet, Sonia Gattei, Valter Bomben, Riccardo |
author_facet | Dereani, Sara Macor, Paolo D’Agaro, Tiziana Mezzaroba, Nelly Dal-Bo, Michele Capolla, Sara Zucchetto, Antonella Tissino, Erika Del Poeta, Giovanni Zorzet, Sonia Gattei, Valter Bomben, Riccardo |
author_sort | Dereani, Sara |
collection | PubMed |
description | Recently it was reported that microRNA from the miR-17 ~ 92 family may have a key role in chronic lymphocytic leukemia (CLL). Here, we designed specific oligonucleotides to target endogenous miR-17 (antagomiR17). In-vitro administration of antagomiR17 effectively reduced miR-17 expression and the proliferation of CLL-like MEC-1 cells. When injected in-vivo in tumor generated by the MEC-1 cells in SCID mice, antagomiR17 dramatically reduced tumor growth and significantly increase survival. Altogether, our results provide the rationale for the use of antagomiR17 as a novel potential therapeutic tool in CLL and in other lymphoproliferative disorders where miR-17 has a driver role in tumor progression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13045-014-0079-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4210490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42104902014-10-29 Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia Dereani, Sara Macor, Paolo D’Agaro, Tiziana Mezzaroba, Nelly Dal-Bo, Michele Capolla, Sara Zucchetto, Antonella Tissino, Erika Del Poeta, Giovanni Zorzet, Sonia Gattei, Valter Bomben, Riccardo J Hematol Oncol Letter to the Editor Recently it was reported that microRNA from the miR-17 ~ 92 family may have a key role in chronic lymphocytic leukemia (CLL). Here, we designed specific oligonucleotides to target endogenous miR-17 (antagomiR17). In-vitro administration of antagomiR17 effectively reduced miR-17 expression and the proliferation of CLL-like MEC-1 cells. When injected in-vivo in tumor generated by the MEC-1 cells in SCID mice, antagomiR17 dramatically reduced tumor growth and significantly increase survival. Altogether, our results provide the rationale for the use of antagomiR17 as a novel potential therapeutic tool in CLL and in other lymphoproliferative disorders where miR-17 has a driver role in tumor progression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13045-014-0079-z) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-23 /pmc/articles/PMC4210490/ /pubmed/25339346 http://dx.doi.org/10.1186/s13045-014-0079-z Text en © Dereani et al.; licensee BioMed Central Ltd. 2014 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Letter to the Editor Dereani, Sara Macor, Paolo D’Agaro, Tiziana Mezzaroba, Nelly Dal-Bo, Michele Capolla, Sara Zucchetto, Antonella Tissino, Erika Del Poeta, Giovanni Zorzet, Sonia Gattei, Valter Bomben, Riccardo Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia |
title | Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia |
title_full | Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia |
title_fullStr | Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia |
title_full_unstemmed | Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia |
title_short | Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia |
title_sort | potential therapeutic role of antagomir17 for the treatment of chronic lymphocytic leukemia |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210490/ https://www.ncbi.nlm.nih.gov/pubmed/25339346 http://dx.doi.org/10.1186/s13045-014-0079-z |
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