The Distribution of the Philadelphia Chromosome in Patients with Chronic Myelogenous Leukemia

JACQUELINE WHANG(National Institutes of Health), Emil Frei(National Institutes of Health), J. H. Tjio(National Institute of Arthritis and Musculoskeletal and Skin Diseases), Paul P. Carbone(National Institutes of Health), George Brecher(National Institute of Arthritis and Musculoskeletal and Skin Diseases)
Blood
December 1, 1963
Cited by 295Open Access
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Abstract

Abstract Thirteen patients with chronic myelogenous leukemia continued to have the Ph1 chromosomes in 90-100 per cent dividing marrow cells during drug-induced clinical remissions. The Ph1 chromosome was present in erythroid as well as granulocytic marrow cells, and possibly in megakaryocytes. The presence of Ph1 chromosomes was also studied in cultures of peripheral blood. In six patients in relapse, 40 per cent of metaphases contained the Ph1 chromosome, and the percentage of these cells corresponded roughly to the relative frequency of immature granulocytes in the blood. In contrast, during remission, few or no Ph1 chromosomes were found in peripheral blood cultures, presumably because in the absence of immature granulocytes the dividing cells in the cultures originate from lymphocytes, as they do in normal blood. It is suggested that the Ph1 chromosome usually arises in a precursor cell common to the erythroid, granulocytic, and megakaryocytic, but not the lymphoid series of hemopoietic cells.


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