Thymidylate synthase protein expression and activity are related to the cell proliferation rate in human cancer cell lines.

M Derenzini, L Montanaro, D Treré, A Chillà, P L Tazzari, F Dall'Olio, D Ofner
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引用次数: 31

Abstract

Aims: To ascertain whether the expression and enzyme activity of thymidylate synthase (TS) are related to the rapidity of cell proliferation in human cancer cell lines.

Methods: Ten asynchronously growing human cancer cell lines of different origin were used, characterised by various doubling times. TS expression was evaluated by western blot analysis using the TS 106 monoclonal antibody. TS activity was determined by the enzyme catalytic assay. The quantitative variation of TS in different phases of the cell cycle was investigated using two parameter flow cytometry for the TS protein and DNA analysis. The number of proliferating cells was evaluated by Ki67 immunostaining.

Results: TS expression and activity were significantly related to each other (r = 0.765; p = 0.01) and to the cell doubling time (r = -0.899; p < 0.001 and r = -0.919; p < 0.001, respectively). Ki67 immunolabelling showed no association between the number of cycling cells and TS protein expression and activity. Two parameter flow cytometry indicated that differences of TS expression in the cell lines were not related to the cell cycle phases or to the proportion of S phase cells.

Conclusions: These results show that the expression and activity of the TS protein in asynchronously growing cancer cells are significantly related to the cell doubling time; the faster the cell proliferation, the greater the expression and activity of TS. These findings could explain why TS values are of prognostic value per se and why tumours with high TS expression benefit more from chemotherapy.

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胸苷酸合成酶蛋白的表达和活性与人癌细胞的增殖速率有关。
目的:探讨胸苷酸合成酶(thymidylate synthase, TS)的表达和酶活性是否与人癌细胞增殖速度有关。方法:采用10株不同来源的非同步生长的人癌细胞系,以不同的倍增次数为特征。western blot检测TS 106单克隆抗体的表达。用酶催化法测定TS活性。采用双参数流式细胞术对TS蛋白和DNA进行分析,研究TS在细胞周期不同时期的定量变化。Ki67免疫染色法检测增殖细胞数量。结果:TS表达与活性呈显著相关(r = 0.765;P = 0.01)和细胞倍增时间(r = -0.899;P < 0.001, r = -0.919;P < 0.001)。Ki67免疫标记显示,循环细胞数量与TS蛋白表达和活性之间无相关性。两参数流式细胞术显示,TS在细胞系中的表达差异与细胞周期和S期细胞比例无关。结论:这些结果表明,TS蛋白在非同步生长癌细胞中的表达和活性与细胞倍增时间显著相关;细胞增殖越快,TS的表达和活性越高。这些发现可以解释为什么TS值本身具有预后价值,以及为什么高TS表达的肿瘤从化疗中获益更多。
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