首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Tumor promoters stimulate hyperplasia of microtubule organizing center and inhibit DNA synthesis in cultured cells.
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Tumor promoters stimulate hyperplasia of microtubule organizing center and inhibit DNA synthesis in cultured cells.

机译:肿瘤启动子刺激微管组织中心的增生并抑制培养细胞中的DNA合成。

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摘要

Chemical tumor promoters induce significant morphologic changes in several cultured cell models. In this article we describe a new effect of two potent, chemically different tumor promoters, 12-O-tetradecanoylphorbol-13-acetate (TPA) and dihydroteleocidin B (DHTB) on cultured human HeLa and melanoma cells. Using immunofluorescence microscopy, we observed that TPA and DHTB induced a dramatic increase in the size (greater than or equal to 3X normal diameter) of the centrosome, a microtubule-organizing center, within 24 h of incubation. In HeLa cells the effect was serum- and dose-dependent, was observed in 76-92% of cells within 72 h of incubation, and was associated with an increase in cytoplasm-nucleus ratio and proliferation of microtubules from the centrosome. The tumor promoters inhibited serum-induced DNA synthesis in both cell lines. Electron microscopy revealed the presence of clumps of microcentriole bodies or fragments adjacent to the intact centriole.
机译:化学肿瘤启动子在几种培养的细胞模型中诱导明显的形态学变化。在本文中,我们描述了两种有效的化学上不同的肿瘤启动子12-O-十四烷酰phorbol-13-乙酸盐(TPA)和二氢teleocidin B(DHTB)对培养的人HeLa和黑素瘤细胞的新作用。使用免疫荧光显微镜,我们观察到TPA和DHTB在孵育24小时内诱导了一个微管组织中心的中心体大小(大于或等于3倍正常直径)的急剧增加。在HeLa细胞中,该作用是血清和剂量依赖性的,在孵育72小时内在76-92%的细胞中观察到了这种作用,并且与细胞质核比的增加和中心体中微管的增殖有关。肿瘤启动子抑制了两种细胞系中血清诱导的DNA合成。电子显微镜检查显示存在完整中心附近的微小中心体团块或碎片。

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