Mcneil Truman Raleigh, Sikder Sweta, Dalal Yamini
Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA.
Open Biol. 2025 May;15(5):240388. doi: 10.1098/rsob.240388. Epub 2025 May 14.
Micronuclei exhibit defective proteomes rendering their chromatin vulnerable to fragmentation. This fragmentation process, known as chromothripsis, promotes tumorigenesis by catalysing the activation of oncogenes and the silencing of tumor suppressors. With this role in mind, micronuclei serve as promising targets for therapeutic intervention. This review will explore recent discoveries regarding how micronuclei form, their function in catalysing chromothripsis and how chromothripsis provides a selective advantage for cancer cells.
微核表现出有缺陷的蛋白质组,使其染色质容易发生片段化。这种片段化过程,即染色体碎裂,通过催化癌基因的激活和肿瘤抑制因子的沉默来促进肿瘤发生。考虑到微核的这一作用,它有望成为治疗干预的靶点。本综述将探讨关于微核如何形成、其在催化染色体碎裂中的作用以及染色体碎裂如何为癌细胞提供选择性优势的最新发现。