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模型系统和癌症中核大小调节的机制。

Mechanisms of nuclear size regulation in model systems and cancer.

机构信息

Department of Molecular Biology, University of Wyoming, 1000 E. University Avenue, Laramie, WY, 82071, USA,

出版信息

Adv Exp Med Biol. 2014;773:537-69. doi: 10.1007/978-1-4899-8032-8_25.

Abstract

Changes in nuclear size have long been used by cytopathologists as an important parameter to diagnose, stage, and prognose many cancers. Mechanisms underlying these changes and functional links between nuclear size and malignancy are largely unknown. Understanding mechanisms of nuclear size regulation and the physiological significance of proper nuclear size control will inform the interplay between altered nuclear size and oncogenesis. In this chapter we review what is known about molecular mechanisms of nuclear size control based on research in model experimental systems including yeast, Xenopus, Tetrahymena, Drosophila, plants, mice, and mammalian cell culture. We discuss how nuclear size is influenced by DNA ploidy, nuclear structural components, cytoplasmic factors and nucleocytoplasmic transport, the cytoskeleton, and the extracellular matrix. Based on these mechanistic insights, we speculate about how nuclear size might impact cell physiology and whether altered nuclear size could contribute to cancer development and progression. We end with some outstanding questions about mechanisms and functions of nuclear size regulation.

摘要

核大小的变化一直被细胞病理学家用作诊断、分期和预测许多癌症的重要参数。这些变化的机制以及核大小与恶性肿瘤之间的功能联系在很大程度上尚不清楚。了解核大小调节的机制以及适当控制核大小的生理意义将阐明改变的核大小与肿瘤发生之间的相互作用。在本章中,我们综述了基于酵母、非洲爪蟾、四膜虫、果蝇、植物、小鼠和哺乳动物细胞培养等模型实验系统的研究,对核大小控制的分子机制的了解。我们讨论了核大小如何受 DNA 倍性、核结构成分、细胞质因子和核质转运、细胞骨架和细胞外基质的影响。基于这些机制上的认识,我们推测核大小可能如何影响细胞生理学,以及改变的核大小是否可能导致癌症的发生和发展。最后,我们提出了一些关于核大小调节机制和功能的悬而未决的问题。

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