Hübner G, Battmer K, Paaz U, Link H
Department of Haematology and Oncology, Hanover University, Medical School, Germany.
Br J Haematol. 1993 Oct;85(2):320-5. doi: 10.1111/j.1365-2141.1993.tb03173.x.
DNA-fingerprint (DNA-F) analysis was successfully performed with DNA from 22 adult patients with acute leukaemia, including 13 patients with acute myeloid leukaemia (AML) and nine patients with acute lymphoblastic leukaemia (ALL). The purpose of this study was to detect differences between the leukaemic phase (at diagnosis or relapse) and remission-phase DNA. We applied one simple repeat probe (GTG)5 and one minisatellite (M13) after DNA-digestion with different restriction endonucleases (HinfI and HaeIII) and agarose gel electrophoresis. In 7/13 patients with AML and 5/9 patients with ALL it was possible to detect loss of bands, additional bands or band shift with at least one of the probes. Together the probes M13 and (GTG)5 unveiled deviating fingerprint patterns in 54.6% of patients between leukaemic cells and remission-phase leucocytes. Allogeneic bone marrow transplantation was performed on six patients. In each case the DNA-F pattern of the donor was different from the relapse and the remission-phase pattern. We conclude from our studies that the probes M13 and (GTG)5 are useful in the detection of relapse and remission in acute leukaemias after chemotherapy and bone marrow transplantation.
对22例成年急性白血病患者的DNA进行了DNA指纹(DNA-F)分析,其中包括13例急性髓细胞白血病(AML)患者和9例急性淋巴细胞白血病(ALL)患者。本研究的目的是检测白血病期(诊断时或复发时)与缓解期DNA之间的差异。在用不同的限制性内切酶(HinfI和HaeIII)消化DNA并进行琼脂糖凝胶电泳后,我们应用了一种简单重复探针(GTG)5和一种小卫星探针(M13)。在13例AML患者中的7例和9例ALL患者中的5例中,使用至少一种探针有可能检测到条带缺失、额外条带或条带移位。探针M13和(GTG)5共同揭示了54.6%的患者白血病细胞与缓解期白细胞之间存在不同的指纹图谱。对6例患者进行了异基因骨髓移植。在每种情况下,供体的DNA-F模式都与复发期和缓解期模式不同。我们从研究中得出结论,探针M13和(GTG)5可用于检测化疗和骨髓移植后急性白血病的复发和缓解情况。