Schirmer Eric C, Latonen Leena, Tollis Sylvain
Institute of Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Institute of Biomedicine, University of Eastern Finland, Kuopio, Finland.
Front Cell Dev Biol. 2022 Oct 10;10:1022723. doi: 10.3389/fcell.2022.1022723. eCollection 2022.
Research on metastasis has recently regained considerable interest with the hope that single cell technologies might reveal the most critical changes that support tumor spread. However, it is possible that part of the answer has been visible through the microscope for close to 200 years. Changes in nuclear size characteristically occur in many cancer types when the cells metastasize. This was initially discarded as contributing to the metastatic spread because, depending on tumor types, both increases and decreases in nuclear size could correlate with increased metastasis. However, recent work on nuclear mechanics and the connectivity between chromatin, the nucleoskeleton, and the cytoskeleton indicate that changes in this connectivity can have profound impacts on cell mobility and invasiveness. Critically, a recent study found that reversing tumor type-dependent nuclear size changes correlated with reduced cell migration and invasion. Accordingly, it seems appropriate to now revisit possible contributory roles of nuclear size changes to metastasis.
近期,随着人们希望单细胞技术能够揭示支持肿瘤扩散的最关键变化,对转移的研究再度引起了广泛关注。然而,部分答案可能在近200年来一直就在显微镜下可见。当细胞发生转移时,许多癌症类型的细胞核大小会发生特征性变化。最初,这一现象被认为与转移扩散无关,因为根据肿瘤类型的不同,细胞核大小的增加和减少都可能与转移增加相关。然而,最近关于核力学以及染色质、核骨架和细胞骨架之间连接性的研究表明,这种连接性的变化可能对细胞迁移和侵袭产生深远影响。至关重要的是,最近一项研究发现,逆转肿瘤类型依赖的细胞核大小变化与细胞迁移和侵袭能力的降低相关。因此,现在重新审视细胞核大小变化对转移可能产生的作用似乎是恰当的。