Avtor/Urednik		Laake, Kirsten; Launonen, Virpi; Niederacher, Dieter; Gudlaugsdottir, Sigfridur; Seitz, Susanne; Rio, Pascale; Champeme, Marie-Helene; Bieche, Ivan; Sever, Nataša; Peterlin, Borut; et al, ;
Naslov		Loss of heterozygosity at 11q23.1 and survival in breast cancer: results of a large European study
Tip		članek
Vir		Genes Chromosomes Cancer
Vol. in št.		Letnik 25, št. 3
Leto izdaje		1999
Obseg		str. 212-21
Jezik		eng
Abstrakt		Among the chromosomal regions commonly undergoing deletions in breast tumours is 11q23.1. The genes that are targets for loss of heterozygosity (LOH) in this region is not yet established. One of the candidate genes located in this region is ATM, responsible for the rare autosomal recessive disorder ataxia-teleangiectasia (A-T).. Interestingly, A-T heterozygotes may have an increased risk of cancer, in particular breast cancer, although this is still controversial. A common assumption has been that the target for the LOH at 11q23.1 in breast carcinoma is the ATM gene, but the area studied has been too large, the density of markers too low, and the number of tumors studied has been too small to draw any firm conclucions. The present study is a multicenter study including 918 breast cancer patients with clinical information and survival data available for most of them. Primary breast tumors were investigated for LOH using a high density of microsatellite markers spanning approximately 6 Mb around the ATM gene. Survival analyses showed that there are most likely one or more candidate genes in a 3-4 Mb region between the markers D11S1819 and D11S927 including the ATM gene. Cancer-specific survival was significantly reduced in patients whose tumors exhibited LOH of markers D11S2179 (within the ATM gene), D11S1778, D11S1294, and D11S1818. The highest survival hazard rations were 1.8 (Cl 1.2-2.8, P = 0.010) and 2.1 (Cl 1.4-3.0, P = 0.0004) for markers D 11S2179 and D11S1818, respectively. One or more of these markers are therefore most likely to be located close to or within genes associated with breast cancer survival.
Deskriptorji		BREAST NEOPLASMS CHROMOSOMES, HUMAN, PAIR 11 ALLELES CARCINOMA, INFILTRATING DUCT CHROMOSOME MAPPING GENETIC MARKERS TRANSLOCATION (GENETICS) SURVIVAL RATE