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头颈部鳞状细胞癌细胞系中的DNA倍性与蛋白质合成

DNA ploidy and protein synthesis in squamous cell carcinoma cell lines of the head and neck.

作者信息

Görögh T, Lippert B M, Sprenger E, Saffran S, Heidorn K, Bergmann G, Henze E, Werner J A

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, University of Kiel, Germany.

出版信息

J Cancer Res Clin Oncol. 1997;123(1):39-44. doi: 10.1007/BF01212613.

Abstract

Aneuploidy as abnormal nuclear DNA content, is considered almost positive evidence of malignancy. In this study three diploid and three aneuploid squamous cell carcinoma (SCC) cell lines were examined for DNA content by flow cytometry. The DNA indices of the SCC cell lines were found to range from 1.0 to 2.1. The mitotic activity of the diploid cell lines was 1.6 times higher and the cells were smaller than aneuploid cells. To find a molecular basis for these differences, the pattern of the de-novo synthesized proteins was analyzed by means of [35S]methionine incorporation, electrophoresis, and autoradiography. In all aneuploid SCC cell lines tested in this experiment, the increase of nuclear DNA content is associated with the synthesis of a novel protein with a molecular mass of approximate 55 kDa as well as with altered synthesis rates of two preexisting proteins (50 kDa and 100 kDa). For determination of the amino acid uptake in diploid and aneuploid cells, the accumulation of [35S]methionine was measured as a function of time by liquid scintillation counting. No significant difference was found in the uptake rate between diploid and aneuploid cells with the same protein content. However, discrepancies were revealed when equal numbers of cells with different DNA index were used, suggesting, that protein turnover is different in diploid and aneuploid SCC cells.

摘要

非整倍体作为异常的核DNA含量,几乎被视为恶性肿瘤的肯定证据。在本研究中,通过流式细胞术检测了三个二倍体和三个非整倍体鳞状细胞癌(SCC)细胞系的DNA含量。发现SCC细胞系的DNA指数范围为1.0至2.1。二倍体细胞系的有丝分裂活性比非整倍体细胞高1.6倍,且细胞体积更小。为了找到这些差异的分子基础,通过[35S]甲硫氨酸掺入、电泳和放射自显影分析了从头合成蛋白质的模式。在本实验中测试的所有非整倍体SCC细胞系中,核DNA含量的增加与一种分子量约为55 kDa的新蛋白质的合成以及两种现有蛋白质(50 kDa和100 kDa)合成速率的改变有关。为了测定二倍体和非整倍体细胞中的氨基酸摄取,通过液体闪烁计数测量了[35S]甲硫氨酸的积累随时间的变化。在蛋白质含量相同的二倍体和非整倍体细胞之间,摄取率没有显著差异。然而,当使用具有不同DNA指数的相同数量的细胞时,发现了差异,这表明二倍体和非整倍体SCC细胞中的蛋白质周转不同。

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