Real-time RT-PCR for the detection and quantification of AML1/MTG8 fusion transcripts in t(8;21)-positive AML patients

被引:49
作者
Krauter, J
Wattjes, MP
Nagel, S
Heidenreich, O
Krug, U
Kafert, S
Bunjes, D
Bergmann, L
Ganser, A
Heil, G
机构
[1] Hannover Med Sch, Dept Haematol Oncol, D-30623 Hannover, Germany
[2] Univ Tubingen, Inst Cell Biol, Dept Mol Biol, D-72074 Tubingen, Germany
[3] Univ Ulm, Dept Internal Med 3, D-89069 Ulm, Germany
关键词
AML; karyotype; RT-PCR; chemotherapy; minimal residual disease;
D O I
10.1046/j.1365-2141.1999.01674.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AML1/MTG8 eras quantified relative to the expression of the GAPDH housekeeping gene by real-time RT-PCR in 22 patients with t(8;21)-positive acute myeloblastic leukaemia (AML) at initial diagnosis and in seven of these patients also during/after chemotherapy and allogeneic bone marrow transplantation. Real-time PCR was able to specifically detect and quantify AML1/MTG8 over a 5 log range. The detection limit far t(8;21)-positive cells was a dilution of 1:10(5). The AML1/MTG8 expression varied considerably among the 22 AML patients at intial diagnosis with a ratio AML1/MTG8:GAPDH of 0.5135 +/- 0.536 (range 0.1-2.14, median 0.318). In six patients with t(8;21)positive ANO; a marked decline of AML1/MTG8 could be induced by chemotherapy. These patients are in ongoing complete haematological remission (CR) with a constant low-level AML1/MTG8 expression. In another patient a rapid rise of AML1/MTG8 transcripts could be detected in CR after allogeneic bone marrow transplantation and the patient relapsed 10 weeks later. In conclusion, real-time RT-PCR is a suitable approach for the quantification of AML1/MTG8 transcripts in the monitoring of AML patients with t(8:21) during/after chemotherapy and can provide data of prognostic relevance.
引用
收藏
页码:80 / 85
页数:6
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