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首页> 外文期刊>BMC Cell Biology >Immortalized cells and one oncogene in malignant transformation: old insights on new explanation
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Immortalized cells and one oncogene in malignant transformation: old insights on new explanation

机译:永生化细胞和一种癌基因正处于恶性转化中:对新解释的旧见解

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Background Nearly thirty years ago, it was first shown that malignant transformation with single oncogene necessarily requires the immortal state of the cell. From that time this thesis for the cells of human origin was not disproved. The basic point which we want to focus on by this short communication is the correct interpretation of the results obtained on the widely used human embryonic kidney 293 (HEK293) cells. Results Intensive literature analysis revealed an increasing number of recent studies discovering new oncogenes with non-overlapping functions. Since the 1970s, dozens of oncogenes have been identified in human cancer. Cultured cell lines are often used as model systems in these experiments. In some investigations the results obtained on such cells are interpreted by the authors as a malignant transformation of normal animal or even normal human cells (as for example with HEK293 cells). However, when a cell line gains the ability to undergo continuous cell division, the cells are not normal any more, they are immortalized cells. Nevertheless, the authors consider these cells as normal human ones, what is basically incorrect. Moreover, it was early demonstrated that the widely used human embryonic kidney 293 (HEK293) cells have a relationship to neurons. Conclusions Thus, the experiments with established cell lines reinforce the notion that immortality is an essential requirement for malignant transformation that cooperates with other oncogenic changes to program the neoplastic state and substances under such investigation should be interpreted as factors which do not malignantly transform normal cells alone, but possess the ability to enhance the tumorigenic potential of already immortalized cells.
机译:背景技术大约三十年前,首次显示单一癌基因的恶性转化必然需要细胞的永生状态。从那时起,有关人类细胞的论文一直没有被驳斥。我们希望通过这种简短的交流来关注的基本点是对广泛使用的人类胚胎肾293(HEK293)细胞获得的结果的正确解释。结果大量的文献分析表明,越来越多的研究发现了具有不重叠功能的新癌基因。自1970年代以来,已在人类癌症中鉴定出数十种致癌基因。在这些实验中,通常将培养的细胞系用作模型系统。在一些研究中,作者将在此类细胞上获得的结果解释为正常动物甚至正常人细胞(例如HEK293细胞)的恶性转化。但是,当细胞系具有进行连续细胞分裂的能力时,这些细胞不再正常,它们是永生化的细胞。然而,作者认为这些细胞是正常的人类细胞,这基本上是错误的。此外,早期证明广泛使用的人胚胎肾293(HEK293)细胞与神经元有关。结论因此,建立细胞系的实验强化了以下观点:永生性是恶性转化的基本要求,恶性转化与其他致癌变化协同作用以编程形成肿瘤状态,在这种研究下,应将物质解释为不会单独恶性转化正常细胞的因素。 ,但具有增强已经永生化细胞的致瘤潜能的能力。

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