INCREASED TYROSINE PROTEIN-KINASE ACTIVITY IN HAIRY-CELL AND MONOCYTIC LEUKEMIAS

被引:7
|
作者
LOWER, EE [1 ]
FRANCO, RS [1 ]
MARTELO, OJ [1 ]
机构
[1] UNIV CINCINNATI,COLL MED,DEPT INTERNAL MED,DIV HEMATOL ONCOL,CINCINNATI,OH 45221
来源
AMERICAN JOURNAL OF THE MEDICAL SCIENCES | 1992年 / 303卷 / 06期
关键词
TYROSINE KINASE; LEUKEMIA;
D O I
10.1097/00000441-199206000-00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tyrosine protein kinases (TPK) help regulate cellular growth and differentiation. Several proto-oncogenes encode for protein products with associated tyrosine kinase activity. An assay for TPK activity was performed in cell extracts using a synthetic peptide substrate and [P-32] adenosine triphosphate (ATP). TPK activity was elevated in K-562 cells, which possess an amplified c-abl oncogene, compared to normal blood mononuclear cells (K-562 = 9.37 +/- 1.72 [mean +/- standard deviation] pmol ATP/10(6) cells/min; normal = 1.14 +/- 0.46, p < 0.01). TPK activity was measured in peripheral blood mononuclear cells from patients with hairy cell leukemia (HCL), myelomonocytic leukemia (MOL), acute myeloblastic leukemia (AML), and chronic lymphocytic leukemia (CLL). In patients with clinically active disease, elevated TPK activity was measured in mononuclear cells from five HCL patients (range 3.76-24.15) and from seven MOL patients. These elevated levels appeared to parallel disease activity, as low levels of TPK activity were measured in patients with inactive (treated) disease. Low levels of TPK were measured in mononuclear cells from active AML and CLL patients. Elevated TPK levels in patients with HCL and MOL may reflect the overexpression of a proto-oncogene or increased growth factor activity in immature or rapidly dividing leukemic cells. Serial TPK levels in HCL and MOL patients correlated with change in disease activity.
引用
收藏
页码:387 / 391
页数:5
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