抑制真核核糖体生物发生:为基础研究和医学应用挖掘新工具

IF 4.1 3区 生物学 Q2 CELL BIOLOGY
Lisa Kofler, Michael Prattes, Helmut Bergler
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引用次数: 0

摘要

新核糖体的形成是每个活细胞的基本细胞过程,与细胞周期控制和增殖紧密交织在一起。该途径的最小干扰可导致核糖体疾病,包括增加某些癌症类型的风险。因此,靶向核糖体生物发生是癌症治疗中的一种新兴策略。然而,由于其复杂性,我们才刚刚开始了解核糖体生物发生途径的动力学。一种新兴的方法是使用靶向化学抑制,它将帮助我们接受形成新核糖体所需的紧密及时的级联事件。然而,到目前为止,只有极少数核糖体生物发生途径的特异性化学抑制剂被鉴定出来。在这里,我们回顾了我们最近发表的筛选,以确定酵母中核糖体生物发生途径的新抑制剂(Awad et al.,2019,BMC Biology)。这些抑制剂可以为基础研究提供新的工具,并可以作为开发新的化疗药物的起点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibiting eukaryotic ribosome biogenesis: Mining new tools for basic research and medical applications.

The formation of new ribosomes is a fundamental cellular process for each living cell and is tightly interwoven with cell cycle control and proliferation. Minimal disturbances of this pathway can result in ribosomopathies including an increased risk for certain cancer types. Thus, targeting ribosome biogenesis is an emerging strategy in cancer therapy. However, due to its complex nature, we are only at the beginning to understand the dynamics of the ribosome biogenesis pathway. One arising approach that will help us to embrace the tight timely cascade of events that is needed to form a new ribosome is the use of targeted chemical inhibition. However, only very few specific chemical inhibitors of the ribosome biogenesis pathway have been identified so far. Here we review our recently published screen to identify novel inhibitors of the ribosome biogenesis pathway in yeast (Awad et al., 2019, BMC Biology). These inhibitors can provide novel tools for basic research and can serve as starting-points to develop new chemotherapeutics.

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来源期刊
Microbial Cell
Microbial Cell Multiple-
CiteScore
6.40
自引率
0.00%
发文量
32
审稿时长
12 weeks
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