mdm-2癌蛋白在乳腺肿瘤(GI-101)原发和转移部位的表达。

Cancer biochemistry biophysics Pub Date : 1999-07-01
P Rathinavelu, A Malavé, S R Raney, J Hurst, C T Roberson, A Rathinavelu
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引用次数: 0

摘要

我们检测了mdm-2癌蛋白(p90)在人类乳腺肿瘤异种移植细胞系(GI-101)中的表达,该细胞系来源于一名57岁复发性浸润性导管腺癌(IIIa期,T3N2MX)的女性癌症患者。免疫沉淀偶联western blot分析了移植胸腺裸鼠的原发肿瘤,使用mdm-2 (Ab-1)小鼠单克隆抗体,初步发现了一个90 kD全长mdm-2蛋白的高水平表达。在GI-101肿瘤中,全长mdm-2 (p90)蛋白的表达水平随着肿瘤大小的增加而增加(100 ~ 2000 mm(3)),在2000 mm(3)的肿瘤中表达量最大。除了在原发部位表达外,在肺和肝组织中也检测到mdm-2蛋白(p90)的显著高水平表达,这是已知的GI-101异种移植肿瘤的转移部位。然而,在对照组小鼠的肺和肝组织中检测不到mdm-2蛋白的表达水平。从GI-101异种移植肿瘤中获得的细胞系(GI-101A)在经过几代传代后也显示出mdm-2蛋白的高水平表达。当GI-101A细胞用己烯雌酚(DES)处理10分钟后,mdm-2蛋白表达增加,并在40分钟时达到峰值。有趣的是,与未处理的细胞相比,DES(10和20微米)处理96小时后也增加了细胞总数。由此可见,mdm-2 (p90)可能在支持GI-101A细胞的肿瘤细胞生长和转移过程中发挥重要作用。
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Expression of mdm-2 oncoprotein in the primary and metastatic sites of mammary tumor (GI-101) implanted athymic nude mice.

The expression of mdm-2 oncoprotein (p90) was determined in a human breast tumor xenograft line (GI-101) that was derived from a 57 year old female cancer patient with recurrent, infiltrating ductal adenocarcinoma (Stage IIIa, T3N2MX). Immunoprecipitation coupled western blot analysis of the primary tumors that have been obtained from xenograft implanted athymic nude mice, using mdm-2 (Ab-1) mouse monoclonal antibody, primarily revealed high level expression of a 90 kD full length mdm-2 protein. In the GI-101 tumor the level of full length mdm-2 (p90) protein expression increased with the increase in the size of the tumor (100 to 2,000 mm(3)) and a maximum expression was detected in 2,000 mm(3) size tumors. In addition to the expression in the primary site, a significantly high level expression of mdm-2 protein (p90) was detected in the lung and liver tissues also, which are the known metastatic sites for GI-101 xenograft tumors. However, the level of mdm-2 protein expression was undetectable in the lung and liver tissues obtained from control mice. A cell line (GI-101A) derived from the GI-101 xenograft tumor also showed a high level expression of mdm-2 protein after several generations of cell passage. When the GI-101A cells were treated with DES (Diethylstilbestrol) the mdm-2 protein expression increased after 10 min treatment and reached a peak level at 40 min. Interestingly, DES (10 and 20 microM) treatment increased the total cell number also after 96 hr treatment compared to the non-treated cells. It appears that mdm-2 (p90) may have a significant role in supporting the tumor cell growth as well as the metastatic process of the GI-101A cells.

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