Increased methotrexate polyglutamylation in acute megakaryocytic leukemia (M7) compared to other subtypes of acute myelocytic leukemia

被引:13
作者
Argiris, A
Longo, GSA
Gorlick, R
Tong, W
Steinherz, P
Bertino, JR
机构
[1] MEM SLOAN KETTERING CANC CTR,DEPT MOL PHARMACOL & THERAPEUT,NEW YORK,NY 10021
[2] MEM SLOAN KETTERING CANC CTR,DEPT PEDIAT,NEW YORK,NY 10021
[3] BETH ISRAEL MED CTR,DEPT MED,NEW YORK,NY 10003
关键词
acute myelocytic leukemia; acute megakaryocytic leukemia; methotrexate; polyglutamylation;
D O I
10.1038/sj.leu.2400647
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acute myelocytic leukemia (AML) is a malignancy that is intrinsically resistant to methotrexate (MTX). AML blasts, when incubated with radiolabeled MTX, form lower amounts of long chain polyglutamates compared to acute lymphocytic leukemia (ALL) blasts, thus providing an explanation far their lack of responsiveness to MTX. Leukemic blasts obtained from two children with acute megakaryocytic leukemia (M7 subtype) when incubated with radiolabeled MTX showed increased accumulation ai total as well as long chain MTX polyglutamates, comparable to levels previously demonstrated in another subtype of AML, acute monocytic leukemia (M5), as well as in blasts from patients with pre-B ALL. We suggest that M7-AML patients with blasts showing increased MTX polyglutamylation might benefit from treatment with MTX.
引用
收藏
页码:886 / 889
页数:4
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