Candidate tumor-suppressor genes on chromosome arm 8p in early-onset and high-grade breast cancers

被引:90
作者
Armes, JE [1 ]
Hammet, F
de Silva, M
Ciciulla, J
Ramus, SJ
Soo, WK
Mahoney, A
Yarovaya, N
Henderson, MA
Gish, K
Hutchins, AM
Price, GR
Venter, DJ
机构
[1] St Vincents Hosp, Dept Anat Pathol, Fitzroy, Vic 3065, Australia
[2] Victorian Breast Canc Res Consortium, Mol Pathol Lab, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
[4] Royal Childrens Hosp, Canc Genom Lab, Murdoch Childrens Res Inst, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Peter MacCallum Canc Inst, Melbourne, Vic 3010, Australia
[6] Univ Melbourne, Dept Surg, Melbourne, Vic 3010, Australia
[7] Prot Design Labs, Fremont, CA 94555 USA
[8] Womens & Childrens Hlth, Melbourne, Vic 3053, Australia
基金
英国医学研究理事会;
关键词
breast cancer; comparative genomic hybridization; expression microarrays; tumor-suppressor genes; chromosome; 8;
D O I
10.1038/sj.onc.1207740
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Loss of genetic material from chromosome arm 8p occurs commonly in breast carcinomas, suggesting that this region is the site of one or more tumor-suppressor genes (TSGs). Comparative genomic hybridization analysis showed that 8p loss is more common in breast cancers from pre-menopausal compared with post-menopausal patients, as well as in high-grade breast cancers, regardless of the menopausal status. Subsequent high-resolution gene expression profiling of genes mapped to chromosome arm 8p, on an extended cohort of clinical tumor samples, indicated a similar dichotomy of breast cancer clinicopathologic types. Some of these genes showed differential downregulation in early-onset and later-onset, high-grade cancers compared with lower-grade, later-onset cancers. Three such genes were analysed further by in situ technologies, performed on tissue microarrays representing breast tumor and normal tissue samples. PCM1, which encodes a centrosomal protein, and DUSP4/MKP-2, which encodes a MAP kinase phosphatase, both showed frequent gene and protein loss in carcinomas. In contrast, there was an excess of cases showing loss of expression in the absence of reduced gene copy number of SFRP1, which encodes a dominant-negative receptor for Wnt-family ligands. These candidate TSGs may constitute some of the molecular drivers of chromosome arm 8p loss in breast carcinogenesis.
引用
收藏
页码:5697 / 5702
页数:6
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