Blood · 1988 · 69 citations · 24 references
Life SciencesGeneticsOncologyCytogeneticsHematologic OncologyOncogenesChromosomal AberrationsChromosomal AbnormalitiesChromosome AberrationsMyelodysplastic SyndromesOncogene ActivationStructural Chromosome AbnormalitiesAberrant Ras ActivationAcute Myeloid Leukemia ProgressionChromosomal Abnormality DetectionChromosomal Abnormality RiskLeukemia CytogeneticsOncogenic Ras MutationsOncogenic Ras SignalingRas-driven Tumorigenesis
The relationship between chromosomal abnormality and oncogene activation was investigated during leukemic progression in two patients with myelodysplastic syndrome (MDS). Both patients had partial or complete deletion of chromosome 5 in metaphase cells obtained throughout the progression to leukemia. Analysis with specific oligonucleotide probes revealed that bone marrow cells containing an activated N-ras oncogene proliferated in a dominant manner during the process of leukemic conversion in both patients. These observations suggest that the chromosomal abnormality may precede activation of the N-ras gene in these patients, and that both the chromosomal abnormality and the activated N-ras oncogene contribute to the development of leukemia.
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Proposals for the classification of the myelodysplastic syndromes
John M. Bennett, Daniel Catovsky, MT Daniel et al. · British Journal of Haematology · 1982 · 3.7K citations
Medicine, Hematology, Pathology +12
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
J Groffen, John Stephenson, Nora Heisterkamp et al. · Cell · 1984 · 1.6K citations
Distinct haematological disorder with deletion of long arm of No. 5 chromosome
Herman Van den Berghe, Jean‐Jacques Cassiman, Guido David et al. · Nature · 1974 · 442 citations
Life Sciences, Genetics, Hematology +14
Prognostic implications of morphology and karyotype in primary myelodysplastic syndromes
Jacobs Rh, MA Cornbleet, JW Vardiman et al. · Blood · 1986 · 243 citations · Full text
Life Sciences, Genetics, Hematology +14