PrLZ, a novel prostate-specific and androgen-responsive gene of the TPD52 family, amplified in chromosome 8q21.1 and overexpressed in human prostate cancer

被引:91
作者
Wang, RX
Xu, JC
Saramäki, O
Visakorpi, T
Sutherland, WM
Zhou, JG
Sen, B
Lim, SD
Mabjeesh, N
Amin, M
Dong, JT
Petros, JA
Nelson, PS
Marshall, FF
Zhau, HE
Chung, LWK
机构
[1] Emory Univ, Sch Med, Dept Urol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Winship Canc Inst, Atlanta, GA 30322 USA
[4] Univ Tampere, Inst Med Technol, Canc Genet Lab, Tampere, Finland
[5] Tampere Univ Hosp, Tampere, Finland
[6] Univ Virginia, Sch Med, Dept Cell Biol, Charlottesville, VA USA
[7] Univ Washington, Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98195 USA
关键词
D O I
10.1158/0008-5472.CAN-03-3331
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report a previously unrecognized prostate-specific protein, PrLZ (prostate leucine zipper), a new member of the Tumor Protein D52 (TPD52) family. The gene for PrLZ was localized at chromosome 8q21.1 a locus most frequently amplified in human prostate cancer. Multiple tissue analyses demonstrated PrLZ predominantly in the prostate gland. Although its expression was enhanced by androgens in androgen receptor-expressing cells, PrLZ was detected in all of the human prostate cancer cell lines, regardless of androgen receptor status. Monoclonal anti-PrLZ antibodies were produced and intense immunohistochemical staining of PrLZ was observed in prostate epithelial cells in intraepithelial neoplasia and prostate cancer, whereas lower-level staining was detected in normal and benign epithelial components of the prostate gland. As the only prostate-specific gene identified in the most frequently amplified genomic region in prostate cancer, PrLZ may be the link between chromosome 8q amplification and malignant transformation of the prostate epithelia.
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页码:1589 / 1594
页数:6
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