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Leuk Res ; 26(11): 979-84, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12363464

ABSTRACT

The c-kit mutation Asp-816-->Val is detectable not only in neoplastic mast cells (MCs) in patients with systemic mastocytosis (SM) but also in most associated hematologic non-MC lineage disease (AHNMD). In order to prove a monoclonal disease evolution we investigated DNA of pooled microdissected single cells for the presence of the mutation in a patient with SM and concomitant chronic myelomonocytic leukemia (CMML). LightCycler melting curve analysis and direct sequencing of nested polymerase chain reaction (PCR) products revealed the c-kit mutation in tryptase-positive MC and in leukemic CD15-positive cells in bone marrow infiltrates, but not in colonic epithelial cells, thus, suggesting a monoclonal evolution of SM and concurrent CMML on the basis of a somatic mutation in a common hematologic progenitor.


Subject(s)
Leukemia, Myelomonocytic, Chronic/genetics , Mastocytosis, Systemic/genetics , Point Mutation , Proto-Oncogene Proteins c-kit/genetics , Aged , Aspartic Acid/genetics , Bone Marrow Cells/pathology , DNA Primers/chemistry , DNA, Neoplasm/genetics , Epithelial Cells/metabolism , Humans , Immunoenzyme Techniques , Lasers , Leukemia, Myelomonocytic, Chronic/complications , Leukemia, Myelomonocytic, Chronic/pathology , Male , Mast Cells/pathology , Mastocytosis, Systemic/complications , Mastocytosis, Systemic/pathology , Polymerase Chain Reaction , Valine/genetics
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