GM-CSF INCUBATION PRIOR TO TREATMENT WITH CYTARABINE OR DOXORUBICIN ENHANCES DRUG ACTIVITY AGAINST AML CELLS-INVITRO - A MODEL FOR LEUKEMIA CHEMOTHERAPY

被引:49
作者
BUTTURINI, A
SANTUCCI, MA
GALE, RP
PEROCCO, P
TURA, S
机构
[1] UNIV CALIF LOS ANGELES, DEPT MED, DIV HEMATOL ONCOL, LOS ANGELES, CA 90024 USA
[2] UNIV PARMA, DEPT PEDIAT, I-43100 PARMA, ITALY
[3] UNIV BOLOGNA, DEPT HEMATOL, I-40126 BOLOGNA, ITALY
[4] UNIV BOLOGNA, DEPT ONCOL, I-40126 BOLOGNA, ITALY
关键词
D O I
10.1016/0145-2126(90)90066-I
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We studied the effect of preincubation with recombinant GM-CSF on the activity of cytarabine and doxorubicin against clonogenic acute myeloid leukemia cells (CFU-AML). Leukemia cells from seven persons with AML, three myeloid cell lines (HL60, KG1, K562) and two control cell lines (U937, MOLT3) were tested. Preincubation with GM-CSF (0.01-0.1 μg/ml) increased DNA synthesis as measured by tritiated thymidine incorporation and intranuclear Ki67 expression in cells from six persons with AML and in HL60 cells. Leukemia cells preincubated with GM-CSF for 6-48 h were exposed to cytarabine (2-200 μg/ml) or doxorubicin (0.01-0.1 μg/ml) for 3 h and CFU-AML assayed. This approach further reduced CFU-AML in samples from six persons with AML and in HL60 and KG1 cells compared to cells not preincubated with GM-CSF prior to drug treatment. In most instances, reduced CFU-AML correlated with GM-CSF induced DNA synthesis. These data suggest a possible strategy of GM-CSF pretreatment to increase anti-leukemia efficacy of chemotherapy in AML. © 1990.
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收藏
页码:743 / 749
页数:7
相关论文
共 28 条
[1]  
ANDREEF M, 1990, IN PRESS ACUTE LEUKE, V2
[2]  
ANTIN JH, 1988, BLOOD, V72, P705
[3]  
BUCHNER T, 1990, IN PRESS ACUTE LEUKE, V2
[4]  
BUTTURINI A, 1987, PROGR BONE MARROW TR, P413
[5]  
CANNISTRA SA, 1989, LEUKEMIA, V3, P328
[6]  
CHAMPLIN R, 1987, BLOOD, V69, P1551
[7]  
DELWEL R, 1988, BLOOD, V72, P1944
[8]  
ESTEY E, 1990, IN PRESS ACUTE LEUKE, V2
[9]  
GRIFFIN JD, 1984, BLOOD, V63, P904
[10]  
GRIFFIN JD, 1986, BLOOD, V68, P1185