PMID- 15120910 OWN - NLM STAT- MEDLINE DCOM- 20040609 LR - 20061115 IS - 0165-4608 (Print) IS - 0165-4608 (Linking) VI - 151 IP - 1 DP - 2004 May TI - Genetic and pathologic significance of 1p, 17p, and 18q aneusomy and the ERBB2 gene in colorectal cancer and related normal colonic mucosa. PG - 52-9 AB - Among chromosome defects in colon cancer, deletions in 1p, 17p, and 18q have been reported as frequent events. To verify this, we investigated 1p, 17p, and 18q aneusomy in 60 colorectal cancers and their surrounding mucosa by means of fluorescence in situ hybridization (FISH). We also evaluated ERBB2 gene (alias HER-2/neu) amplification in a subset of tumors. The genetic picture in tumors was correlated with chromosomal alterations in normal colonic mucosae, as well with clinicopathologic variables. A population of cells in morphologically normal epithelium possesses genetic aberrations common to those in colon cancer, although in different percentages. No significant difference emerged in terms of fraction of nuclei with 17p monosomy between primary tumors and distal mucosal samples. Of tumor samples aneusomic for the three chromosomes, 58.3% also showed aneusomy in related normal colonic mucosa. In neoplastic samples, significant correlation existed between 1p aneusomy and mucosal component (P<0.007), between 17p aneusomy and increased depth of invasion (T3-T4) (P<0.05), and between 18q aneusomy and tumor site (P<0.03). None of the evaluated samples, neoplastic or normal, showed ERBB2 gene amplification. FAU - Cianciulli, A AU - Cianciulli A AD - Department of Clinical Pathology, Regina Elena Cancer Institute, IFO Via Elio Chianesi 53, 00144 Rome, Italy. cianciulli@ifo.it FAU - Cosimelli, M AU - Cosimelli M FAU - Marzano, R AU - Marzano R FAU - Merola, R AU - Merola R FAU - Piperno, G AU - Piperno G FAU - Sperduti, I AU - Sperduti I FAU - de la Iglesia, F AU - de la Iglesia F FAU - Leonardo, G AU - Leonardo G FAU - Graziano, F AU - Graziano F FAU - Mancini, R AU - Mancini R FAU - Guadagni, F AU - Guadagni F LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Cancer Genet Cytogenet JT - Cancer genetics and cytogenetics JID - 7909240 SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - *Chromosomes, Human, Pair 1 MH - *Chromosomes, Human, Pair 17 MH - *Chromosomes, Human, Pair 18 MH - Colon/*metabolism MH - Colorectal Neoplasms/*genetics MH - Female MH - Gene Amplification MH - *Genes, erbB-2 MH - Humans MH - In Situ Hybridization, Fluorescence MH - Intestinal Mucosa/metabolism MH - Male MH - Middle Aged EDAT- 2004/05/04 05:00 MHDA- 2004/06/21 10:00 CRDT- 2004/05/04 05:00 PHST- 2003/06/02 00:00 [received] PHST- 2003/09/08 00:00 [revised] PHST- 2003/09/15 00:00 [accepted] PHST- 2004/05/04 05:00 [pubmed] PHST- 2004/06/21 10:00 [medline] PHST- 2004/05/04 05:00 [entrez] AID - S0165460803004187 [pii] AID - 10.1016/j.cancergencyto.2003.09.013 [doi] PST - ppublish SO - Cancer Genet Cytogenet. 2004 May;151(1):52-9. doi: 10.1016/j.cancergencyto.2003.09.013.