British journal of haematology · 2013
Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
Клинический случайСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Fernandez-Mercado Marta, Pellagatti Andrea, Di Genua Cristina, Larrayoz Maria Jose, Winkelmann Nils, Aranaz Paula, Burns Adam, Schuh Anna, Calasanz Maria Jose, Cross Nicholas C P, Boultwood Jacqueline
Аннотация
Whole exome sequencing was performed in a patient with myelodysplastic syndrome before and after progression to acute myeloid leukaemia. Mutations in several genes, including SETBP1, were identified following leukaemic transformation. Screening of 328 patients with myeloid disorders revealed SETBP1 mutations in 14 patients (4·3%), 7 of whom had -7/del(7q) and 3 had i(17)(q10), cytogenetic markers associated with shortened overall survival and increased risk of leukaemic evolution. SETBP1 mutations were frequently acquired at the time of leukaemic evolution, coinciding with increase of leukaemic blasts. These data suggest that SETBP1 mutations may play a role in MDS and chronic myelomonocytic leukaemia disease progression.
Предметные рубрики MeSH
Biomarkers, TumorCarrier ProteinsCell Transformation, NeoplasticChromosome AberrationsChromosome DeletionChromosomes, Human, Pair 7Disease ProgressionExomeHeterozygoteHigh-Throughput Nucleotide SequencingHumansLeukemia, Myelomonocytic, ChronicMaleMutationMyelodysplastic SyndromesNuclear ProteinsRecurrence