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Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations
Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) with genomic aberrations has been shown to resemble lymphoma-type adult T-cell leukemia/lymphoma (ATLL) in terms of its genomic aberration patterns, histopathology, and prognosis. We have shown recently that a majority of patients with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544466/ https://www.ncbi.nlm.nih.gov/pubmed/23342278 http://dx.doi.org/10.1002/cam4.34 |
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author | Yoshida, Noriaki Umino, Akira Liu, Fang Arita, Kotaro Karube, Kennosuke Tsuzuki, Shinobu Ohshima, Koichi Seto, Masao |
author_facet | Yoshida, Noriaki Umino, Akira Liu, Fang Arita, Kotaro Karube, Kennosuke Tsuzuki, Shinobu Ohshima, Koichi Seto, Masao |
author_sort | Yoshida, Noriaki |
collection | PubMed |
description | Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) with genomic aberrations has been shown to resemble lymphoma-type adult T-cell leukemia/lymphoma (ATLL) in terms of its genomic aberration patterns, histopathology, and prognosis. We have shown recently that a majority of patients with acute-type ATLL have multiple subclones that were likely produced in lymph nodes. In this study, we analyzed whether PTCL, NOS with genomic aberrations also has multiple subclones as found in ATLL by means of high-resolution oligo-array comparative genomic hybridization (CGH). Thirteen cases of PTCL, NOS were available for 44K high-resolution array CGH analysis. The results showed that 11 (84.6%) of the 13 cases had a log2 ratio imbalance, suggesting that multiple subclones exist in PTCL, NOS with genomic aberrations. In order to analyze the association between multiple subclones and prognosis, we used previous bacterial-artificial chromosome (BAC) array analyses for 29 cases and found that the existence of multiple subclones was associated with a poor prognosis (P = 0.0279). |
format | Online Article Text |
id | pubmed-3544466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-35444662013-01-22 Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations Yoshida, Noriaki Umino, Akira Liu, Fang Arita, Kotaro Karube, Kennosuke Tsuzuki, Shinobu Ohshima, Koichi Seto, Masao Cancer Med Cancer Biology Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) with genomic aberrations has been shown to resemble lymphoma-type adult T-cell leukemia/lymphoma (ATLL) in terms of its genomic aberration patterns, histopathology, and prognosis. We have shown recently that a majority of patients with acute-type ATLL have multiple subclones that were likely produced in lymph nodes. In this study, we analyzed whether PTCL, NOS with genomic aberrations also has multiple subclones as found in ATLL by means of high-resolution oligo-array comparative genomic hybridization (CGH). Thirteen cases of PTCL, NOS were available for 44K high-resolution array CGH analysis. The results showed that 11 (84.6%) of the 13 cases had a log2 ratio imbalance, suggesting that multiple subclones exist in PTCL, NOS with genomic aberrations. In order to analyze the association between multiple subclones and prognosis, we used previous bacterial-artificial chromosome (BAC) array analyses for 29 cases and found that the existence of multiple subclones was associated with a poor prognosis (P = 0.0279). WILEY-VCH Verlag 2012-12 2012-09-26 /pmc/articles/PMC3544466/ /pubmed/23342278 http://dx.doi.org/10.1002/cam4.34 Text en © 2012 The Authors. Published by Blackwell Publishing Ltd. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Cancer Biology Yoshida, Noriaki Umino, Akira Liu, Fang Arita, Kotaro Karube, Kennosuke Tsuzuki, Shinobu Ohshima, Koichi Seto, Masao Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations |
title | Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations |
title_full | Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations |
title_fullStr | Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations |
title_full_unstemmed | Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations |
title_short | Identification of multiple subclones in peripheral T-cell lymphoma, not otherwise specified with genomic aberrations |
title_sort | identification of multiple subclones in peripheral t-cell lymphoma, not otherwise specified with genomic aberrations |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544466/ https://www.ncbi.nlm.nih.gov/pubmed/23342278 http://dx.doi.org/10.1002/cam4.34 |
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