Wang Ruoxiang, Xu Jianchun, Saramäki Outi, Visakorpi Tapio, Sutherland William M, Zhou Jianguang, Sen Buer, Lim So Dug, Mabjeesh Nicola, Amin Mahul, Dong Jin-Tang, Petros John A, Nelson Peter S, Marshall Fray F, Zhau Haiyen E, Chung Leland W K
Molecular Urology and Therapeutics, Department of Urology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Cancer Res. 2004 Mar 1;64(5):1589-94. doi: 10.1158/0008-5472.can-03-3331.
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.
我们报告了一种先前未被识别的前列腺特异性蛋白,即PrLZ(前列腺亮氨酸拉链蛋白),它是肿瘤蛋白D52(TPD52)家族的一个新成员。PrLZ基因定位于8号染色体q21.1区域,该位点在人类前列腺癌中最常发生扩增。多种组织分析表明PrLZ主要存在于前列腺中。尽管在表达雄激素受体的细胞中其表达受雄激素增强,但在所有人类前列腺癌细胞系中均检测到PrLZ,无论其雄激素受体状态如何。制备了单克隆抗PrLZ抗体,并且在前列腺上皮内瘤变和前列腺癌的前列腺上皮细胞中观察到PrLZ强烈的免疫组化染色,而在前列腺的正常和良性上皮成分中检测到较低水平的染色。作为在前列腺癌中最常扩增的基因组区域中鉴定出的唯一前列腺特异性基因,PrLZ可能是8号染色体q扩增与前列腺上皮恶性转化之间的联系。