MYCN oncogene amplification in neuroblastoma is statistically associated wi
th gain of chromosome segment 17q21-qter. In neuroblastoma cell lines and p
rimary tumors with MYCN amplification in the form of homogeneously staining
regions (hsrs), juxtaposition of chromosome 17 material with MYCN sequence
s has occasionally been reported, raising the possibility of a physical aff
inity between MYCN and chromosome arm 17q. We used FISH to test for associa
tion between chromosome 17 segments and MYCN in eight neuroblastoma cell li
nes and two neuroblastoma primary tumors known to include hsrs. Evidence of
an association was found in the chromosomes of both primary tumors; in one
, a MYCN hsr was inserted into a structurally abnormal chromosome 17, in th
e other, an hsr in 16p was shown to be flanked by 17 material. In cell line
NCG, hsrs in 4q and 16p were flanked by 17q material. These observations c
onfirm the juxtaposition of 17q material with MYCN sequences in some neurob
lastomas, and imply that there may be a physical or functional relationship
between these two features in MYCN amplified neuroblastoma. (C) 2001 Wiley
-Liss, Inc.