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Killing Me Softly—Future Challenges in Apoptosis Research

机译:温柔地杀了我—细胞凋亡研究的未来挑战

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摘要

The induction of apoptosis, a highly regulated and clearly defined mode of cell dying, is a vital tenet of modern cancer therapy. In this review we focus on three aspects of apoptosis research which we believe are the most crucial and most exciting areas currently investigated and that will need to be better understood in order to enhance the efficacy of therapeutic measures. First, we discuss which target to select for cancer therapy and argue that not the cancer cell as such, but its interaction with the microenvironment is a more promising and genetically stable site of attack. Second, the complexity of combination therapy is elucidated using the PI3-K-mediated signaling network as a specific example. Here we show that the current clinical approach to sensitize malignancies to apoptosis by maximal, prolonged inhibition of so-called survival pathways can actually be counter productive. Third, we propose that under certain conditions which will need to be clearly defined in future, chronification of a tumor might be preferable to the attempt at a cure. Finally, we discuss further problems with utilizing apoptosis induction in cancer therapy and propose a novel potential therapeutic approach that combines the previously discussed features.
机译:凋亡的诱导是一种高度调控且明确定义的细胞死亡方式,是现代癌症治疗的重要宗旨。在这篇综述中,我们着重于凋亡研究的三个方面,我们认为这是当前研究的最关键和最令人兴奋的领域,为了增强治疗措施的有效性,需要更好地理解它们。首先,我们讨论选择哪个目标进行癌症治疗,并认为不是癌细胞本身,而是癌细胞与微环境的相互作用是一个更有希望且遗传稳定的攻击部位。其次,使用PI3-K介导的信号网络作为一个具体例子,阐明了联合治疗的复杂性。在这里,我们表明,通过最大程度地,长期抑制所谓的生存途径使恶性肿瘤对细胞凋亡敏感的当前临床方法实际上可能适得其反。第三,我们建议在将来需要明确定义的某些条件下,肿瘤的定时化可能比治愈的尝试更为可取。最后,我们讨论了在癌症治疗中利用细胞凋亡诱导的其他问题,并提出了一种结合了先前讨论的功能的新型潜在治疗方法。

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