Cyclins of phases G1, S and G2/M are overexpressed in aneuploid mammary carcinomas.

P Collecchi, T Santoni, E Gnesi, A Giuseppe Naccarato, A Passoni, M Rocchetta, R Danesi, G Bevilacqua
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Abstract

Expression of cyclins A, B1 and D1 in human breast cancer was analyzed using dual-parameter flow cytometry with simultaneous evaluation of the DNA content. The asynchronous MCF-7 breast adenocarcinoma cells were used to implement flow cytometry analysis and to analyze the cell cycle distribution of cyclins. The patterns of the cyclin expression were also analyzed in vivo in fresh tissue specimens of human breast carcinomas. The combined measurement of DNA and cyclins showed a higher cyclin expression in aneuploid (11.5 +/- 2.0%, 4.3 +/- 1.1%, and 19.5 +/- 3.4% positive cells for cyclins A, B, and D1, respectively) than in diploid carcinomas (3.9 +/- 1.2%, 1.1 +/- 0.4%, and 5.0 +/- 1.2% positive cells for cyclins A, B, and D1, respectively). A positive relationship was also found between cyclin A and D1 expression and H(3)-thymidine labeling index. In the in vitro model, the asynchronous growing MCF-7 cells showed a variable number of cells expressing cyclins in an unscheduled way, unrelated to the phase at which these cyclins are expressed in normal cells. A similar condition was also observed in tumors. In conclusion, the data showed a deregulated expression of cyclins in a transformed adenocarcinoma cell line and in breast tumors. Furthermore, overexpression of these proteins is related to the aneuploid and high proliferative activity of human mammary carcinomas.

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G1期、S期和G2/M期细胞周期蛋白在非整倍体乳腺癌中过表达。
采用双参数流式细胞术分析细胞周期蛋白A、B1和D1在人乳腺癌组织中的表达,同时测定DNA含量。采用异步MCF-7乳腺腺癌细胞进行流式细胞术分析,分析细胞周期蛋白的细胞周期分布。我们还分析了细胞周期蛋白在人乳腺癌新鲜组织标本体内的表达模式。DNA和细胞周期蛋白的联合测量显示,细胞周期蛋白在非整倍体(细胞周期蛋白a、B和D1分别为11.5 +/- 2.0%、4.3 +/- 1.1%和19.5 +/- 3.4%阳性细胞)中的表达高于二倍体癌(细胞周期蛋白a、B和D1分别为3.9 +/- 1.2%、1.1 +/- 0.4%和5.0 +/- 1.2%阳性细胞)。细胞周期蛋白A和D1的表达与H(3)-胸腺嘧啶标记指数呈正相关。在体外模型中,异步生长的MCF-7细胞显示出不同数量的细胞以非预定的方式表达细胞周期蛋白,与这些细胞周期蛋白在正常细胞中表达的阶段无关。在肿瘤中也观察到类似的情况。总之,数据显示细胞周期蛋白在转化的腺癌细胞系和乳腺肿瘤中的表达不受调控。此外,这些蛋白的过表达与人类乳腺癌的非整倍体和高增殖活性有关。
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