Cytogenetic analysis of short-term cultures from 105 squamous cell carcinom
as of the larynx (LSCC) revealed clonal chromosome aberrations in 56 tumors
. Simple karyotypic changes (less than four aberrations per clone) were fou
nd in 24 cases, and the remaining 32 tumors had complex karyotypes with mul
tiple numerical as well as unbalanced structural rearrangements. Extensive
intratumor heterogeneity, in the Form of multiple related subclones or unre
lated clones, was observed in a large fraction of the tumors. The structura
l changes most often affected chromosomes 3, 1, 11, 7, 2, 15, 5, 4, 8, and
12, with rearrangements in the centromeric regions, i.e., the centromeric b
ands p10 and q10 and the juxtacentromeric bands p11 and q11, accounting for
43% of the total breakpoints. The most common imbalances brought about by
numerical and unbalanced structural rearrangements were loss of chromosomal
region 3p21-pter, chromosome arms 4p, 6q, 8p, 10p, 13p, 14p, 15p, and 17p,
and gain of chromosomal regions 3q21-qter, 7q31-pter, and 8q. Among 17 rec
urrent aberrations identified, the most common were i(8q), hsr(11)(q13), i(
3q), i(5p), and del(3)(p11). No statistically significant association was f
ound between major karyotypic features and histological differentiation or
TNM stage. The karyotypic features of the LSCC were also compared with prev
iously published oral SCC, a subgroup of SCC that has been more extensively
characterized cytogenetically. No clear-cut karyotypic differences were fo
und between LSCC and oral SCC, with the exception that i(8q) was significan
tly more frequent among the latter. Genes Chromosomes Cancer 28:66-76, 2000
. (C) 2000 Wiley-Liss, Inc.