Premium
Correlation between 1p deletions and aneusomy in human colorectal adenomas
Author(s) -
Di Vinci Angela,
Infusini Edmondo,
Peveri Consuelo,
Sciutto Andrea,
Geido Elio,
Risio Mauro,
Rossini Francesco P.,
Giaretti Walter
Publication year - 1998
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/(sici)1097-0215(19980105)75:1<45::aid-ijc8>3.0.co;2-1
Subject(s) - correlation , colorectal cancer , medicine , oncology , biology , cancer , mathematics , geometry
Human sporadic colorectal adenomas are characterized by a relatively high occurrence of aneuploidy. Similarly, 1p deletions have been reported to be an early event in colorectal tumorigenesis, while chromosome 7, 17 and 18 gain/losses were also found. The present study investigated 1p deletions, the numerical aberrations of chromosomes 1, 7, 17 and 18, and the nuclear DNA content as obtained by flow cytometry in a series of 34 human sporadic colorectal adenomas. From these adenomas, 51 intra‐adenoma regions were microdissected according to 2 degrees of dysplasia and presence of foci of early cancer. Isolated epithelial nuclei were analyzed by fluorescence in situ hybridization interphase cytogenetics using centromeric probes for chromosomes 7, 17 and 18 and, in a double‐target analysis, a centromeric probe for chromosome 1 simultaneously with a telomeric probe mapping to the 1p36 band. Aneuploidy incidence due to presence of numerical aberrations for at least one among the investigated chromosomes and/or abnormal flow‐cytometric DNA content was 35%, while 1p deletion incidence was 38%. The correlation of 1p deletions with aneuploidy was statistically highly significant ( p = 0.003), suggesting that loss of genes in this region may be implicated in chromosome instability. Int. J. Cancer 75:45–50, 1998.© 1998 Wiley‐Liss, Inc.