R. Dubinsky et al., FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) FOR RETROSPECTIVE DETECTIONOF TRISOMY-3 AND TRISOMY-7 IN MULTIPLE-MYELOMA, Cancer genetics and cytogenetics, 83(2), 1995, pp. 115-118
The malignant plasma cells of multiple myeloma (MM) have a low prolife
rative activity and therefore cytogenetic studies of the disease have
been severely limited. We evaluated the role of fluorescence in situ h
ybridization (FISH) in the detection of numerical chromosomal abnormal
ities in early stages of myeloma and the applicability of the method t
o stored archival slides. Old air-dried bone marrow smears From 15 mye
loma patients obtained at presentation were probed with a satellite DN
A sequences to chromosomes 3 and 7. Numerical chromosome aberrations w
ere found in eight (53%) of the patients, including six (of 12) with t
risomy 7, and two (of eight) with trisomy 3. This study demonstrates t
hat FISH is a sensitive method for the detection of numerical aberrati
ons in myeloma and for the study of old slides for retrospective analy
sis.