G. Hubner et al., MONITORING OF RELAPSE AND REMISSION IN ACUTE LEUKEMIAS BY DNA-FINGERPRINT ANALYSIS, British Journal of Haematology, 85(2), 1993, pp. 320-325
DNA-fingerprint (DNA-F) analysis was successfully performed with DNA f
rom 22 adult patients with acute leukaemia, including 13 patients with
acute myeloid leukaemia (AML) and nine patients with acute lymphoblas
tic leukaemia (ALL). The purpose of this study was to detect differenc
es between the leukaemic phase (at diagnosis or relapse) and remission
-phase DNA. We applied one simple repeat probe (GTG)5 and one minisate
llite (M13) after DNA-digestion with different restriction endonucleas
es (HinfI and HaeIII) and agarose gel electrophoresis. In 7/13 patient
s with AML and 5/9 patients with ALL. it was possible to detect loss o
f bands, additional bands or band shift with at least one of the probe
s. Together the probes M13 and (GTG)5 unveiled deviating fingerprint p
atterns in 54-6% of patients between leukaemic cells and remission-pha
se leucocytes. Allogeneic bone marrow transplantation was performed on
six patients. In each case the DNA-F pattern of the donor was differe
nt 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 b
one marrow transplantation.