The t(1;3) breakpoint-spanning involved in clear cell renal cell genes LSAMP and NORE1 are carcinomas

被引:95
作者
Chen, JD
Lui, WO
Vos, MD
Clark, GJ
Takahashi, M
Schoumans, J
Khoo, SK
Petillo, D
Lavery, T
Sugimura, J
Astuti, D
Zhang, C
Kagawa, S
Maher, ER
Larsson, C
Alberts, AS
Kanayama, HO
Teh, BT [1 ]
机构
[1] Van Andel Res Inst, Canc Genet Lab, Grand Rapids, MI 49503 USA
[2] Van Andel Res Inst, Lab Cell Struct & Signal Integrat, Grand Rapids, MI 49503 USA
[3] Karolinska Hosp, Dept Mol Med, SE-17176 Stockholm, Sweden
[4] NCI, Dept Cell & Canc Biol, NIH, Rockville, MD 20850 USA
[5] Univ Tokushima, Sch Med, Dept Urol, Tokushima 770, Japan
[6] Univ Birmingham, Sch Med, Canc Res UK Renal Mol Oncol Res Grp, Sect Med & Mol Genet, Birmingham, W Midlands, England
关键词
D O I
10.1016/S1535-6108(03)00269-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
By positional cloning, we identified two breakpoint-spanning genes in a familial clear cell renal cell carcinoma (CCRCC)-associated t(1;3)(q32.1;q13.3): LSAMP and NORE1 (RASSF1 homolog). Both genes are downregulated in 9 of 9 RCC cell lines. While the NORE1A promoter predominantly presents partial methylation in 6 of the cell lines and 17/53 (32%) primary tumors, the LSAMP promoter is completely methylated in 5 of 9 cell lines and in 14/53 (26%) sporadic and 4 familial CCRCCs. Expression of LSAMP and NORE1 A proteins in CCRCC cell lines inhibited cell proliferation. These characteristics indicate that LSAMP and NORE1A may represent new candidate tumor suppressors for CCRCC.
引用
收藏
页码:405 / 413
页数:9
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