CDC91L1 (PIG-U) is a newly discovered oncogene in human bladder cancer

被引:72
作者
Guo, ZM
Linn, JF
Wu, GJ
Anzick, SL
Eisenberger, CF
Halachmi, S
Cohen, Y
Fomenkov, A
Hoque, MO
Okami, K
Steiner, G
Engles, JM
Osada, M
Moon, C
Ratovitski, E
Trent, JM
Meltzer, PS
Westra, WH
Kiemeney, LA
Schoenberg, MP
Sidransky, D [1 ]
Trink, B
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Div Head & Neck Canc Res, Baltimore, MD 21205 USA
[2] NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA
[3] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] Univ Med Ctr, Dept Urol, Dept Epidemiol & Biostat, NL-6500 HB Nijmegen, Netherlands
[6] Johns Hopkins Univ Hosp, Inst Med, Dept Urol, James Buchanan Brady Urol Inst, Baltimore, MD 21205 USA
关键词
D O I
10.1038/nm1010
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
Genomic amplification at 20q11-13 is a common event in human cancers. We isolated a germline translocation breakpoint at 20q11 from a bladder cancer patient. We identified CDC91L1, the gene encoding CDC91L1 (also called phosphatidylinositol glycan class U (PIG-U), a transamidase complex unit in the glycosylphosphatidylinositol (GPI) anchoring pathway), as the only gene whose expression was affected by the translocation. CDC91L1 was amplified and overexpressed in about one-third of bladder cancer cell lines and primary tumors, as well as in oncogenic uroepithelial cells transformed with human papillomavirus (HPV) E7. Forced overexpression of CDC91L1 malignantly transformed NIH3T3 cells in vitro and in vivo. Overexpression of CDC91L1 also resulted in upregulation of the urokinase receptor (uPAR), a GPI-anchored protein, and in turn increased STAT-3 phosphorylation in bladder cancer cells. Our findings suggest that CDC91L1 is an oncogene in bladder cancer, and implicate the GPI anchoring system as a potential oncogenic pathway and therapeutic target in human cancers.
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收藏
页码:374 / 381
页数:8
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