Molecular Haematology Unit, Radcliffe Department of Medicine, The MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
Department of Oncology, The MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
Genes (Basel). 2021 Oct 29;12(11):1734. doi: 10.3390/genes12111734.
The study of the molecular pathways underlying cancer has given us important insights into how breaks in our DNA are repaired and the dire consequences that can occur when these processes are perturbed. Extensive research over the past 20 years has shown that the key molecular event underpinning a subset of cancers involves the deregulated repair of DNA double-strand breaks (DSBs) at telomeres, which in turn leads to telomere lengthening and the potential for replicative immortality. Here we discuss, in-depth, recent major breakthroughs in our understanding of the mechanisms underpinning this pathway known as the alternative lengthening of telomeres (ALT). We explore how this gives us important insights into how DSB repair at telomeres is regulated, with relevance to the cell-cycle-dependent regulation of repair, repair of stalled replication forks and the spatial regulation of DSB repair.
该研究的分子途径为基础的癌症给了我们重要的见解,如何打破我们的 DNA 修复和可怕的后果,可能发生时,这些过程受到干扰。过去 20 年来的广泛研究表明,关键的分子事件的基础上的子集的癌症涉及失调的修复 DNA 双链断裂 (DSBs) 在端粒,这反过来又导致端粒延长和潜在的复制永生。在这里,我们深入讨论,在过去的重大突破,在我们的理解机制的基础上,这条途径称为替代延长端粒 (ALT)。我们探讨如何这给了我们重要的见解,如何 DSB 修复端粒是监管,与细胞周期的监管有关的修复,修复停滞复制叉和空间调控 DSB 修复。