Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Crown St, Liverpool L69 3BX, U.K.
Division of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, U.K.
Biochem Soc Trans. 2019 Oct 31;47(5):1209-1222. doi: 10.1042/BST20190034.
Due to cell-cycle dysregulation, many cancer cells contain more than the normal compliment of centrosomes, a state referred to as centrosome amplification (CA). CA can drive oncogenic phenotypes and indeed can cause cancer in flies and mammals. However, cells have to actively manage CA, often by centrosome clustering, in order to divide. Thus, CA is also an Achilles' Heel of cancer cells. In recent years, there have been many important studies identifying proteins required for the management of CA and it has been demonstrated that disruption of some of these proteins can cause cancer-specific inhibition of cell growth. For certain targets therapeutically relevant interventions are being investigated, for example, small molecule inhibitors, although none are yet in clinical trials. As the field is now poised to move towards clinically relevant interventions, it is opportune to summarise the key work in targeting CA thus far, with particular emphasis on recent developments where small molecule or other strategies have been proposed. We also highlight the relatively unexplored paradigm of reversing CA, and thus its oncogenic effects, for therapeutic gain.
由于细胞周期失调,许多癌细胞含有超过正常数量的中心体,这种状态被称为中心体扩增(CA)。CA 可以驱动致癌表型,实际上可以在果蝇和哺乳动物中引发癌症。然而,细胞必须积极地管理 CA,通常通过中心体聚集来进行分裂。因此,CA 也是癌细胞的阿喀琉斯之踵。近年来,有许多重要的研究确定了管理 CA 所需的蛋白质,并且已经证明破坏其中一些蛋白质可以导致针对癌细胞生长的特异性抑制。对于某些具有治疗意义的靶点,正在研究治疗相关的干预措施,例如小分子抑制剂,尽管目前尚无临床试验。由于该领域现在准备进行具有临床意义的干预,因此适时总结迄今为止针对 CA 的关键工作特别强调了最近提出的小分子或其他策略的新进展。我们还强调了逆转 CA 及其致癌作用以获得治疗益处的相对未被探索的范例。