Genes, chromosomes & cancer · 2013
The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemia.
Клинический случайСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Dobbins Sara E, Sherborne Amy L, Ma Yussanne P, Bardini Michela, Biondi Andrea, Cazzaniga Giovanni, Lloyd Amy, Chubb Daniel, Greaves Mel F, Houlston Richard S
Аннотация
Over 90% of infants (< 1-year-old) diagnosed with leukemia have pro-B acute lymphoblastic leukemia (ALL) containing the MLL-AF4 fusion. When compared with other forms of paediatric ALL affecting later B-cell differentiation, MLL-AF4 pro-B is associated with a dismal prognosis with a typical 5-year disease-free survival of <20%. MLL-AF4 may be sufficient on its own for leukemogenesis or the gene-fusion product may alternatively predispose transformed cells to global genetic instability, enhancing the acquisition of additional key mutations. To gain insight into the genomic landscape of infant MLL-AF4 pro-B ALL we performed whole genome sequencing of diagnostic leukemic blasts and matched germline samples from three MLL-AF4 pro-B ALL infants. Our analysis revealed few somatic changes (copy number abnormalities, loss of heterozygosity, or single nucleotide variants), demonstrating that only a very small number of mutations are necessary to generate infant MLL-leukemia.
Предметные рубрики MeSH
DNA Copy Number VariationsDNA Mutational AnalysisGenome, HumanGenomicsHumansINDEL MutationInfantInfant, NewbornLoss of HeterozygosityMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionPolymorphism, Single NucleotidePrecursor Cell Lymphoblastic Leukemia-LymphomaSequence Analysis, DNATranslocation, Genetic