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Lack of Ku80 Alteration in Multiple Myeloma

Chromosomal rearrangement involving the immunoglobulin gene locus, as a result of marked chromosomal instability, is the hallmark of human multiple myeloma (MM) cells. Since Ku80 plays a key role in the non‐homologous end‐joining (NHEJ) system, we investigated whether Ku80 alteration contributes to...

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Detalles Bibliográficos
Autores principales: Kato, Miyuki, Iida, Shinsuke, Komatsu, Hirokazu, Ueda, Ryuzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927006/
https://www.ncbi.nlm.nih.gov/pubmed/11985783
http://dx.doi.org/10.1111/j.1349-7006.2002.tb01264.x
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author Kato, Miyuki
Iida, Shinsuke
Komatsu, Hirokazu
Ueda, Ryuzo
author_facet Kato, Miyuki
Iida, Shinsuke
Komatsu, Hirokazu
Ueda, Ryuzo
author_sort Kato, Miyuki
collection PubMed
description Chromosomal rearrangement involving the immunoglobulin gene locus, as a result of marked chromosomal instability, is the hallmark of human multiple myeloma (MM) cells. Since Ku80 plays a key role in the non‐homologous end‐joining (NHEJ) system, we investigated whether Ku80 alteration contributes to this genetic instability by examining its status in 16 MM cell lines. Our study demonstrated a lack of Ku80 alterations at the protein, mRNA and gene level in 15 out of the 16 cell lines. Only the U266 cell line carried a missense mutation of Ser335Leu in one allele of the cDNA. Six marrow samples derived from myeloma patients also did not show any aberrant Ku80 protein, in terms of size. Accordingly, Ku80 alteration is unlikely to be involved in MM, in disagreement with a previous study reporting frequent presence of a 69‐kD Ku80 variant (Ku86v) with reduced DNA binding activity in MM cells.
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spelling pubmed-59270062018-05-11 Lack of Ku80 Alteration in Multiple Myeloma Kato, Miyuki Iida, Shinsuke Komatsu, Hirokazu Ueda, Ryuzo Jpn J Cancer Res Article Chromosomal rearrangement involving the immunoglobulin gene locus, as a result of marked chromosomal instability, is the hallmark of human multiple myeloma (MM) cells. Since Ku80 plays a key role in the non‐homologous end‐joining (NHEJ) system, we investigated whether Ku80 alteration contributes to this genetic instability by examining its status in 16 MM cell lines. Our study demonstrated a lack of Ku80 alterations at the protein, mRNA and gene level in 15 out of the 16 cell lines. Only the U266 cell line carried a missense mutation of Ser335Leu in one allele of the cDNA. Six marrow samples derived from myeloma patients also did not show any aberrant Ku80 protein, in terms of size. Accordingly, Ku80 alteration is unlikely to be involved in MM, in disagreement with a previous study reporting frequent presence of a 69‐kD Ku80 variant (Ku86v) with reduced DNA binding activity in MM cells. Blackwell Publishing Ltd 2002-04 /pmc/articles/PMC5927006/ /pubmed/11985783 http://dx.doi.org/10.1111/j.1349-7006.2002.tb01264.x Text en
spellingShingle Article
Kato, Miyuki
Iida, Shinsuke
Komatsu, Hirokazu
Ueda, Ryuzo
Lack of Ku80 Alteration in Multiple Myeloma
title Lack of Ku80 Alteration in Multiple Myeloma
title_full Lack of Ku80 Alteration in Multiple Myeloma
title_fullStr Lack of Ku80 Alteration in Multiple Myeloma
title_full_unstemmed Lack of Ku80 Alteration in Multiple Myeloma
title_short Lack of Ku80 Alteration in Multiple Myeloma
title_sort lack of ku80 alteration in multiple myeloma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927006/
https://www.ncbi.nlm.nih.gov/pubmed/11985783
http://dx.doi.org/10.1111/j.1349-7006.2002.tb01264.x
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