Mouse spectral karyotyping (SKY) was employed to analyze 29 primary BALB/c
plasmacytomas (PCTs) for the presence of chromosomal aberrations that took
place subsequent to the Myc-activating T(12F1;15D2) or T(6C1;15D2) transloc
ations, the initiating oncogenic mutations in plasmacytomagenesis. Recurren
t amplifications of chromosome (Chr) 1 (48% prevalence) and promiscuous non
-reciprocal translocations of Chr 5 (52% prevalence) suggested the existenc
e of important PCT progressor genes on bands I B/C and 5F. The additional o
ccurrence of sporadic aberrations (93% prevalence) most likely reflected th
e general instability of the PCT genome. This instability, however, was not
consistent, as two PCTs lacked secondary cytogenetic changes detectable by
SKY. Our findings led us to conclude that BALB/c PCTs show a remarkably si
milar degree of cytogenetic heterogeneity to human multiple myeloma, despit
e being genetically defined (inbred mouse strain) and uniformly initiated (
deregulation of Myc). Genes Chromosomes Cancer 29:70-74, 2000. Published 20
00 Wiley-Liss, Inc.dagger.