R. Musilova et al., MULTIPLE UNRELATED CLONES IN MYELODYSPLASTIC SYNDROME AND IN ACUTE MYELOID-LEUKEMIA, Cancer genetics and cytogenetics, 88(2), 1996, pp. 141-143
We identified cytogenetically unrelated clones in the bone marrow of 1
2 of 240 patients with myelodysplastic syndrome (MDS) and in 3 of 232
patients with acute myeloid leukemia (AML). In addition, unrelated sin
gle-cell abnormalities were found in six MDS and two AML patients. The
most commonly encountered abnormalities present in the unrelated clon
es in patients with refractory anemia (RA) were del(5q), +8, and -7. I
n blastic types of MDS and AML trisomy 8 was found in two of eight pat
ients while in the remaining cases the chromosome abnormalities were d
iverse and nonspecific. The presence of the chromosomally unrelated cl
ones, together with recent data on the early appearance of monoclonali
ty provided by molecular biology studies, support the interpretation t
hat aberrations such as +8 and del(5q) are actually secondary abnormal
ities that develop during tumor progression in a cell with a primary s
ubmicroscopic genomic rearrangement.