Integrative analysis reveals 53BP1 copy loss and decreased expression in a subset of human diffuse large B-cell lymphomas
p53-Binding protein 1 ( 53BP1 ) encodes a critical checkpoint protein that localizes to sites of DNA double-strand breaks (DSBs) and participates in DSB repair. Mice that are 53bp1 deficient or hemizygous have an increased incidence of lymphoid malignancies. However, 53BP1 abnormalities in primary h...
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Veröffentlicht in: | Oncogene 2008-01, Vol.27 (3), p.318-322 |
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Sprache: | eng |
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Zusammenfassung: | p53-Binding protein 1
(
53BP1
) encodes a critical checkpoint protein that localizes to sites of DNA double-strand breaks (DSBs) and participates in DSB repair. Mice that are
53bp1
deficient or hemizygous have an increased incidence of lymphoid malignancies. However, 53BP1 abnormalities in primary human tumors have not been described. By combining high-density single nucleotide polymorphism (HD SNP) array data and gene expression profiles, we found 9 of 63 newly diagnosed human diffuse large B-cell lymphomas (DLBCLs) with single copy loss of the chromosome 15q15 region including the
53BP1
locus; these nine tumors also had significantly lower levels of
53BP1
transcripts.
53BP1
single copy loss found with the HD SNP array platform was subsequently confirmed by fluorescence
in situ
hybridization. These studies highlight the role of
53BP1
copy loss in primary human DLBCLs and the value of integrative analyses in detecting this genetic lesion in human tumors. |
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ISSN: | 0950-9232 1476-5594 |
DOI: | 10.1038/sj.onc.1210650 |