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Involvement of deleted chromosome 5 in complex chromosomal aberrations in newly diagnosed myelodysplastic syndromes (MDS) is correlated with extremely adverse prognosis

Z. Zemanova, K. Michalova, H. Buryova, J. Brezinova, K. Kostylkova, D. Bystricka, M. Novakova, I. Sarova, S. Izakova, L. Lizcova, S. Ransdorfova, Z. Krejcik, MD. Merkerova, A. Dohnalova, M. Siskova, A. Jonasova, R. Neuwirtova, J. Cermak,

. 2014 ; 38 (5) : 537-44.

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc14063686

MDS with complex chromosomal aberrations (CCA) are characterized by short survival and a high rate of transformation to AML. A comprehensive genome-wide analysis of bone-marrow cells of 157 adults with newly diagnosed MDS and CCA revealed a large spectrum of nonrandom genomic changes related to the advanced stages of MDS. Chromosome shattering, probably resulting from chromothripsis, was found in 47% of patients. Deleted chromosome 5 was unstable and often involved in different types of cryptic unbalanced rearrangements. No true monosomy 5 was observed. Patients with CCA involving deleted chromosome 5 had an extremely poor prognosis (median overall survival, 2 months).

Citace poskytuje Crossref.org

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