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Identification of miR-15b as a transformation-related factor in mantle cell lymphoma

Mantle cell lymphoma (MCL) is an aggressive B cell lymphoma with a poor prognosis. It is characterized by the t(11;14)(q13;q32) translocation, resulting in overexpression of CCND1. Morphologically, MCL is categorised into two types: classical MCL (cMCL) and aggressive MCL (aMCL), with a proportion o...

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Autores principales: ARAKAWA, FUMIKO, KIMURA, YOSHIZO, YOSHIDA, NORIAKI, MIYOSHI, HIROAKI, DOI, ATUSHI, YASUDA, KAORI, NAKAJIMA, KAZUTAKA, KIYASU, JUNICHI, NIINO, DAISUKE, SUGITA, YASUO, TASHIRO, KOSUKE, KUHARA, SATORU, SETO, MASAO, OHSHIMA, KOICHI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725451/
https://www.ncbi.nlm.nih.gov/pubmed/26676972
http://dx.doi.org/10.3892/ijo.2015.3295
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author ARAKAWA, FUMIKO
KIMURA, YOSHIZO
YOSHIDA, NORIAKI
MIYOSHI, HIROAKI
DOI, ATUSHI
YASUDA, KAORI
NAKAJIMA, KAZUTAKA
KIYASU, JUNICHI
NIINO, DAISUKE
SUGITA, YASUO
TASHIRO, KOSUKE
KUHARA, SATORU
SETO, MASAO
OHSHIMA, KOICHI
author_facet ARAKAWA, FUMIKO
KIMURA, YOSHIZO
YOSHIDA, NORIAKI
MIYOSHI, HIROAKI
DOI, ATUSHI
YASUDA, KAORI
NAKAJIMA, KAZUTAKA
KIYASU, JUNICHI
NIINO, DAISUKE
SUGITA, YASUO
TASHIRO, KOSUKE
KUHARA, SATORU
SETO, MASAO
OHSHIMA, KOICHI
author_sort ARAKAWA, FUMIKO
collection PubMed
description Mantle cell lymphoma (MCL) is an aggressive B cell lymphoma with a poor prognosis. It is characterized by the t(11;14)(q13;q32) translocation, resulting in overexpression of CCND1. Morphologically, MCL is categorised into two types: classical MCL (cMCL) and aggressive MCL (aMCL), with a proportion of cMCL progressing to develop into aMCL. miRNAs are currently considered to be important regulators for cell behavior and are deregulated in many malignancies. Although several genetic alterations have been implicated in the transformation of cMCL to aMCL, the involvement of miRNAs in transformation is not known. In an effort to identify the miRNAs related to the transformation of MCL, miRNA microarray analyses were used for cMCL and aMCL cases. These analyses demonstrated significant differences in the expression of seven microRNAs based on a t-test (p-value <0.05); miR-15b was greatly upregulated in aMCL. Locked nucleic acid in situ hybridization showed increased staining of miR-15b in formalin-fixed paraffin-embedded sections of aMCL. These results correlated well with the microRNA microarray analysis. Although the molecular functions of miR-15b are largely unknown, it has been found to be associated with the cell cycle and apoptosis. However, the physiological significance of increased miR-15b in MCL is still unknown. Our present findings suggest that the upregulated expression of miR-15b is likely to play an important role in the transformation of cMCL to aMCL.
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spelling pubmed-47254512016-01-31 Identification of miR-15b as a transformation-related factor in mantle cell lymphoma ARAKAWA, FUMIKO KIMURA, YOSHIZO YOSHIDA, NORIAKI MIYOSHI, HIROAKI DOI, ATUSHI YASUDA, KAORI NAKAJIMA, KAZUTAKA KIYASU, JUNICHI NIINO, DAISUKE SUGITA, YASUO TASHIRO, KOSUKE KUHARA, SATORU SETO, MASAO OHSHIMA, KOICHI Int J Oncol Articles Mantle cell lymphoma (MCL) is an aggressive B cell lymphoma with a poor prognosis. It is characterized by the t(11;14)(q13;q32) translocation, resulting in overexpression of CCND1. Morphologically, MCL is categorised into two types: classical MCL (cMCL) and aggressive MCL (aMCL), with a proportion of cMCL progressing to develop into aMCL. miRNAs are currently considered to be important regulators for cell behavior and are deregulated in many malignancies. Although several genetic alterations have been implicated in the transformation of cMCL to aMCL, the involvement of miRNAs in transformation is not known. In an effort to identify the miRNAs related to the transformation of MCL, miRNA microarray analyses were used for cMCL and aMCL cases. These analyses demonstrated significant differences in the expression of seven microRNAs based on a t-test (p-value <0.05); miR-15b was greatly upregulated in aMCL. Locked nucleic acid in situ hybridization showed increased staining of miR-15b in formalin-fixed paraffin-embedded sections of aMCL. These results correlated well with the microRNA microarray analysis. Although the molecular functions of miR-15b are largely unknown, it has been found to be associated with the cell cycle and apoptosis. However, the physiological significance of increased miR-15b in MCL is still unknown. Our present findings suggest that the upregulated expression of miR-15b is likely to play an important role in the transformation of cMCL to aMCL. D.A. Spandidos 2015-12-15 /pmc/articles/PMC4725451/ /pubmed/26676972 http://dx.doi.org/10.3892/ijo.2015.3295 Text en Copyright: © Arakawa et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Articles
ARAKAWA, FUMIKO
KIMURA, YOSHIZO
YOSHIDA, NORIAKI
MIYOSHI, HIROAKI
DOI, ATUSHI
YASUDA, KAORI
NAKAJIMA, KAZUTAKA
KIYASU, JUNICHI
NIINO, DAISUKE
SUGITA, YASUO
TASHIRO, KOSUKE
KUHARA, SATORU
SETO, MASAO
OHSHIMA, KOICHI
Identification of miR-15b as a transformation-related factor in mantle cell lymphoma
title Identification of miR-15b as a transformation-related factor in mantle cell lymphoma
title_full Identification of miR-15b as a transformation-related factor in mantle cell lymphoma
title_fullStr Identification of miR-15b as a transformation-related factor in mantle cell lymphoma
title_full_unstemmed Identification of miR-15b as a transformation-related factor in mantle cell lymphoma
title_short Identification of miR-15b as a transformation-related factor in mantle cell lymphoma
title_sort identification of mir-15b as a transformation-related factor in mantle cell lymphoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725451/
https://www.ncbi.nlm.nih.gov/pubmed/26676972
http://dx.doi.org/10.3892/ijo.2015.3295
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