Blood · 2012
High-resolution genomic profiling of chronic lymphocytic leukemia reveals new recurrent genomic alterations.
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Edelmann Jennifer, Holzmann Karlheinz, Miller Florian, Winkler Dirk, Bühler Andreas, Zenz Thorsten, Bullinger Lars, Kühn Michael W M, Gerhardinger Andreas, Bloehdorn Johannes, Radtke Ina, Su Xiaoping, Ma Jing, Pounds Stanley, Hallek Michael, Lichter Peter, Korbel Jan, Busch Raymonde, Mertens Daniel, Downing James R, Stilgenbauer Stephan, Döhner Hartmut
Аннотация
To identify genomic alterations in chronic lymphocytic leukemia (CLL), we performed single-nucleotide polymorphism-array analysis using Affymetrix Version 6.0 on 353 samples from untreated patients entered in the CLL8 treatment trial. Based on paired-sample analysis (n = 144), a mean of 1.8 copy number alterations per patient were identified; approximately 60% of patients carried no copy number alterations other than those detected by fluorescence in situ hybridization analysis. Copy-neutral loss-of-heterozygosity was detected in 6% of CLL patients and was found most frequently on 13q, 17p, and 11q. Minimally deleted regions were refined on 13q14 (deleted in 61% of patients) to the DLEU1 and DLEU2 genes, on 11q22.3 (27% of patients) to ATM, on 2p16.1-2p15 (gained in 7% of patients) to a 1.9-Mb fragment containing 9 genes, and on 8q24.21 (5% of patients) to a segment 486 kb proximal to the MYC locus. 13q deletions exhibited proximal and distal breakpoint cluster regions. Among the most common novel lesions were deletions at 15q15.1 (4% of patients), with the smallest deletion (70.48 kb) found in the MGA locus. Sequence analysis of MGA in 59 samples revealed a truncating mutation in one CLL patient lacking a 15q deletion. MNT at 17p13.3, which in addition to MGA and MYC encodes for the network of MAX-interacting proteins, was also deleted recurrently.
Предметные рубрики MeSH
Chromosome AberrationsDNA Copy Number VariationsFemaleGene Expression ProfilingGenomicsHumansImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionIn Situ Hybridization, FluorescenceKaplan-Meier EstimateLeukemia, Lymphocytic, Chronic, B-CellLoss of HeterozygosityMaleMutationOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideTumor Suppressor Protein p53