Department of Urology, Chang Gung Memorial Hospital, Kwei-Shan, Tao-Yuan, Taiwan, ROC.
Prostate. 2012 Sep 15;72(13):1431-42. doi: 10.1002/pros.22494. Epub 2012 Jan 30.
Glycoprotein transmembrane nmb (GPNMB) gene was originally identified in osteoblasts and belongs to the pmel-17/nmb family. The function or regulation of GPNMB in the human prostate remains unknown.
The expression of GPNMB in prostate carcinoma cells were determined by real-time reverse transcription-polymerase chain reaction (RT-qPCR) and immunoblot assays. Effects of ectopic GPNMB overexpression on cell proliferation, invasion, and tumorigenesis were determined by (3) H-thymidine incorporation, matrigel invasion, soft agar cloning assays, and murine xenograft study. Effects of GPNMB, p53, and androgen on target gene were assessed using RT-PCR, immunoblotting, and transient gene expression assays.
In vitro analysis using several prostate cell lines suggested that expression of GPNMB may be relevant to the extent of neoplasia. Ectopic overexpression of GPNMB significantly attenuated cell proliferation and invasion and exerted antitumorigenic activity on PC-3 cells in vitro and in vivo. GPNMB overexpression induced the gene expressions of N-myc downstream regulated gene 1 (Ndrg1) and maspin in PC-3 cells. Doxorubicin treatment or transient overexpression of p53 increased GPNMB expression. Androgen (R1881) treatment has a divergent effect on gene expression of prostate-specific antigen (PSA) and GPNMB in LNCaP cells. Androgen treatment enhanced cell proliferation but downregulated GPNMB protein expression in stably overexpressed androgen receptor (AR) CA-HPV-10 cells.
Together these results suggest that GPNMB gene is a p53- and androgen-dysregulated gene and should be regarded as an anti-tumor gene for prostate cancer. The enhancement of Ndrg1 and maspin gene expressions may account for the anti-proliferative and anti-invasive function of GPNMB in PC-3 cells.
糖蛋白跨膜 nmb(GPNMB)基因最初在成骨细胞中被鉴定出来,属于 pmel-17/nmb 家族。GPNMB 在人前列腺中的功能或调节仍不清楚。
通过实时逆转录-聚合酶链反应(RT-qPCR)和免疫印迹分析确定前列腺癌细胞中 GPNMB 的表达。通过(3)H-胸腺嘧啶掺入、基质胶侵袭、软琼脂克隆测定和小鼠异种移植研究确定过表达 GPNMB 对细胞增殖、侵袭和肿瘤发生的影响。使用 RT-PCR、免疫印迹和瞬时基因表达测定评估 GPNMB、p53 和雄激素对靶基因的影响。
使用几种前列腺细胞系进行的体外分析表明,GPNMB 的表达可能与肿瘤的程度有关。过表达 GPNMB 可显著减弱 PC-3 细胞的增殖和侵袭,并在体外和体内发挥抗肿瘤活性。GPNMB 过表达诱导 PC-3 细胞中 N-myc 下游调节基因 1(Ndrg1)和 maspin 的基因表达。多柔比星处理或瞬时过表达 p53 增加了 GPNMB 的表达。雄激素(R1881)处理对 LNCaP 细胞前列腺特异性抗原(PSA)和 GPNMB 的基因表达有不同的影响。雄激素处理增强了稳定过表达雄激素受体(AR)CA-HPV-10 细胞的细胞增殖,但下调了 GPNMB 蛋白表达。
这些结果表明,GPNMB 基因是一个 p53 和雄激素失调的基因,应被视为前列腺癌的抗肿瘤基因。Ndrg1 和 maspin 基因表达的增强可能解释了 GPNMB 在 PC-3 细胞中的抗增殖和抗侵袭功能。