癌细胞中多余中心粒的阶段性特异性产生。

IF 3.1 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2025-06-01 Epub Date: 2025-04-23 DOI:10.1091/mbc.E24-08-0386
Byungho Shin, Myungse Kim, Yejoo Lee, Kunsoo Rhee
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引用次数: 0

摘要

尽管在有丝分裂过程中存在与灾难性结果相关的潜在风险,但许多癌细胞仍保持着多余的中心粒。在这项研究中,我们寻找在M期产生多余中心粒的癌细胞系,并在十几种检查的细胞系中鉴定出一些细胞系。PLK4活性也是M相特异生成多余中心粒所必需的。我们观察到,在许多癌细胞中,当中心粒周围物质(PCM)蛋白(如PCNT和CEP215)水平较低时,有丝分裂中心粒会过早分离。此外,多余中心粒的存在与有丝分裂PCM水平降低有关。值得注意的是,PCNT的过表达导致MDA-MB-157细胞中多余中心粒的减少。这些发现表明,有丝分裂PCM的减少可能是选择性癌细胞中M期特异性产生多余中心粒的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
M phase-specific generation of supernumerary centrioles in cancer cells.

Many cancer cells maintain supernumerary centrioles, despite the potential risks associated with catastrophic outcomes during mitosis. In this study, we searched for cancer cell lines in which supernumerary centrioles are generated during the M phase and identified a few cell lines among the dozen examined. PLK4 activity is also required for M phase-specific generation of supernumerary centrioles. We observed that mitotic centrioles prematurely separate in many cancer cells when levels of pericentriolar material (PCM) proteins, such as PCNT and CEP215, are low. Furthermore, the presence of supernumerary centrioles was correlated with reduced mitotic PCM levels. Notably, overexpression of PCNT led to a reduction in supernumerary centrioles in MDA-MB-157 cells. These findings suggest that diminution of mitotic PCM may be a cause of M phase-specific generation of supernumerary centrioles in selected cancer cells.

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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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