DELETION OF THE SHORT ARM OF CHROMOSOME-3 IN BREAST-TUMORS

Citation
N. Pandis et al., DELETION OF THE SHORT ARM OF CHROMOSOME-3 IN BREAST-TUMORS, Genes, chromosomes & cancer, 18(4), 1997, pp. 241-245
Citations number
39
Categorie Soggetti
Oncology,"Genetics & Heredity
Journal title
ISSN journal
10452257
Volume
18
Issue
4
Year of publication
1997
Pages
241 - 245
Database
ISI
SICI code
1045-2257(1997)18:4<241:DOTSAO>2.0.ZU;2-H
Abstract
Deletions in the short arm of chromosome 3 have long been known to be common in many tumor types, including carcinomas of the lung and kidne y. Small interstitial deletions of the proximal-central region of 3p, with band 3p 14 as a minimal common deleted segment, have recently bee n shown to occur in as many as 10% of carcinomas of the breast, often as the only chromosomal change. Seemingly identical deletions may also be found in the epithelial cells of mixed-lineage benign tumors of th e breast and even in diffuse proliferative breast disease, a disorder that would not normally be accepted as neoplastic, but never in comple tely normal breast tissue. The cytogenetic evidence therefore indicate s that the putative tumor suppressor gene deleted from 3p14 influences cellular proliferation; evidently, its loss is often not sufficient f or a fully malignant phenotype to emerge. The first information about FHIT, a candidate suppressor gene recently identified in the FRA3B fra gile site in 3p 14 and found to be abnormal or lost in a high percenta ge of carcinomas of various organs, including breast, is compatible wi th such a general proliferation-regulating role. (C) 1997 Wiley-Liss, Inc.