Nucleoporin Gene Fusions and Hematopoietic Malignancies

B. Fahrenkrog
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引用次数: 20

Abstract

Nuclear pore complexes (NPCs) are the sole gateways between the nucleus and the cytoplasm of eukaryotic cells and they mediate all macromolecular trafficking between these cellular compartments. Nucleocytoplasmic transport is highly selective and precisely regulated and as such an important aspect of normal cellular function. Defects in this process or in its machinery have been linked to various human diseases, including cancer. Nucleoporins, which are about 30 proteins that built up NPCs, are critical players in nucleocytoplasmic transport and have also been shown to be key players in numerous other cellular processes, such as cell cycle control and gene expression regulation. This review will focus on the three nucleoporins Nup98, Nup214, and Nup358. Common to them is their significance in nucleocytoplasmic transport, their multiple other functions, and being targets for chromosomal translocations that lead to haematopoietic malignancies, in particular acute myeloid leukaemia. The underlying molecular mechanisms of nucleoporin-associated leukaemias are only poorly understood but share some characteristics and are distinguished by their poor prognosis and therapy outcome.
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核孔蛋白基因融合与造血恶性肿瘤
核孔复合物(NPCs)是真核细胞细胞核和细胞质之间的唯一通道,并介导这些细胞间的所有大分子运输。核细胞质运输具有高度选择性和精确调控,是正常细胞功能的重要方面。这一过程或其机制中的缺陷与包括癌症在内的各种人类疾病有关。核孔蛋白是约30种构建npc的蛋白质,是核胞质运输的关键参与者,也被证明是许多其他细胞过程的关键参与者,如细胞周期控制和基因表达调节。本文主要对三种核孔蛋白Nup98、Nup214和Nup358进行综述。它们的共同之处在于它们在核细胞质运输中的重要性,它们的多种其他功能,以及它们是导致造血恶性肿瘤,特别是急性髓性白血病的染色体易位的靶标。核孔蛋白相关白血病的潜在分子机制尚不清楚,但有一些共同的特点,其预后和治疗结果都很差。
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