Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2138000 | Leukemia Research | 2010 | 6 Pages |
Abstract
A clonal cytogenetic abnormality was observed in Philadelphia chromosome-negative bone marrow cells of 6/27 chronic myeloid leukemia patients (+8 in 4, −7 in 1, and 20q− in 1) with dasatinib-induced remissions. The X-linked human androgen receptor gene assay demonstrated clonality in one additional patient. Single nucleotide polymorphism array analysis revealed somatic uniparental disomy involving chromosome 17(p12-pter) in another patient. The TP53 gene had a 5′ splice site deletion of exon 6 that caused alternative splicing, frame shifting and introduction of a premature stop codon. After three years, no patient developed myelodysplastic syndrome or acute myeloid leukemia.
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Authors
Ronald L. Paquette, John Nicoll, Meenal Chalukya, Lucas Gondek, Monika Jasek, Charles L. Sawyers, Neil P. Shah, Jaroslaw Maciejewski,