Ependymomas are glial cell-derived tumors. They are, in contrast to ot
her gliomas (astrocytomas, oligodendrogliomas, and oligoastrocytomas),
ill-defined with respect to the genes and chromosomal segments import
ant in their tumorigenesis. In this study, we extensively screened 17
ependymomas for genetic changes characteristic of other gliomas. Allel
ic loss was detected on chromosome arm 22q in three tumors; on chromos
ome 10 in two tumors; on chromosome arm 17p in two tumors; and on chro
mosome arms 6q, 9p, 13q, and 19q, each in one tumor. No allelic losses
were found on chromosome arms 1p and 16q, None of the tumors had EGFR
gene amplification. In each case, the chromosomal segment affected by
the deletion included the region known to harbor a tumor suppressor g
ene important in glioma tumorigenesis. We conclude that ependymomas re
semble the other glial neoplasms with respect to type and location of
the chromosomal changes involved. Given the relatively infrequent occu
rrence of these genetic changes, ependymomas should be considered gene
tically as low-grade gliomas. (C) 1995 Wiley-Liss, Inc.