Ivkov Robert, Bunz Fred
a Department of Radiation Oncology and Molecular Radiation Sciences ; The Kimmel Cancer Center at Johns Hopkins ; Baltimore MD USA.
Cell Cycle. 2015;14(18):2886-90. doi: 10.1080/15384101.2015.1068483. Epub 2015 Jul 15.
Chromothripsis is a recently recognized mode of genetic instability that generates chromosomes with strikingly large numbers of segmental re-arrangements. While the characterization of these derivative chromosomes has provided new insights into the processes by which cancer genomes can evolve, the underlying signaling events and molecular mechanisms remain unknown. In medulloblastomas, chromothripsis has been observed to occur in the context of mutational inactivation of p53 and activation of the canonical Hedgehog (Hh) pathway. Recent studies have illuminated mechanistic links between these 2 signaling pathways, including a novel PTCH1 homolog that is regulated by p53. Here, we integrate this new pathway into a hypothetical model for the catastrophic DNA breakage that appears to trigger profound chromosomal rearrangements.
染色体碎裂是一种最近才被认识到的基因不稳定模式,它会产生具有大量片段重排的染色体。虽然对这些衍生染色体的特征描述为癌症基因组进化过程提供了新的见解,但其潜在的信号事件和分子机制仍然未知。在髓母细胞瘤中,已观察到染色体碎裂发生在p53突变失活和经典刺猬(Hh)信号通路激活的背景下。最近的研究揭示了这两条信号通路之间的机制联系,包括一种受p53调控的新型PTCH1同源物。在这里,我们将这条新通路整合到一个假设模型中,该模型用于解释似乎触发深度染色体重排的灾难性DNA断裂。