Department of Oncology, KU Leuven, University of Leuven, LKI, Leuven Cancer Institute, Leuven, Belgium.
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland.
Cancer Discov. 2017 Oct;7(10):1069-1087. doi: 10.1158/2159-8290.CD-17-0550. Epub 2017 Sep 18.
A wealth of novel findings, including congenital ribosomal mutations in ribosomopathies and somatic ribosomal mutations in various cancers, have significantly increased our understanding of the relevance of ribosomes in oncogenesis. Here, we explore the growing list of mechanisms by which the ribosome is involved in carcinogenesis-from the hijacking of ribosomes by oncogenic factors and dysregulated translational control, to the effects of mutations in ribosomal components on cellular metabolism. Of clinical importance, the recent success of RNA polymerase inhibitors highlights the dependence on "onco-ribosomes" as an Achilles' heel of cancer cells and a promising target for further therapeutic intervention. The recent discovery of somatic mutations in ribosomal proteins in several cancers has strengthened the link between ribosome defects and cancer progression, while also raising the question of which cellular mechanisms such defects exploit. Here, we discuss the emerging molecular mechanisms by which ribosomes support oncogenesis, and how this understanding is driving the design of novel therapeutic strategies.
大量新的发现,包括核糖体病中的先天性核糖体突变和各种癌症中的体细胞核糖体突变,极大地提高了我们对核糖体在肿瘤发生中的相关性的理解。在这里,我们探讨了核糖体参与致癌作用的不断增加的机制列表-从致癌因子和失调的翻译控制对核糖体的劫持,到核糖体成分突变对细胞代谢的影响。具有临床重要意义的是,RNA 聚合酶抑制剂的最近成功突出了对“癌核糖体”的依赖性,作为癌细胞的致命弱点和进一步治疗干预的有前途的靶标。最近在几种癌症中发现核糖体蛋白的体细胞突变,加强了核糖体缺陷与癌症进展之间的联系,同时也提出了这样的问题,即这些缺陷利用了哪些细胞机制。在这里,我们讨论了核糖体支持致癌作用的新兴分子机制,以及这种理解如何推动新型治疗策略的设计。