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Arf proteins in cancer cell migration

机译:Arf蛋白在癌细胞迁移中的作用

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摘要

Members of the ADP-ribosylation factor (Arf) family of small OTP-binding (G) proteins regulate several aspects of membrane trafficking, such as vesicle budding, tethering and cytoskeleton organization. Arf family members, including Arf-like (Art) proteins have been implicated in several essential cellular functions, like cell spreading and migration. These functions are used by cancer cells to disseminate and invade the tissues surrounding the primary tumor, leading to the formation of metastases. Indeed, Arf and Arl proteins, as well as their guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) have been found to be abnormally expressed in different cancer cell types and human cancers. Here, we review the current evidence supporting the involvement of Arf family proteins and their GEFs and GAPs in cancer progression, focusing on 3 different mechanisms: cell-cell adhesion, integrin internalization and recycling, and actin cytoskeleton remodeling.
机译:小OTP结合(G)蛋白的ADP-核糖基化因子(Arf)家族成员调节膜运输的多个方面,例如囊泡发芽,束缚和细胞骨架组织。 Arf家族成员,包括Arf样(Art)蛋白已经牵涉到一些基本的细胞功能,例如细胞扩散和迁移。癌细胞利用这些功能来传播和侵袭原发肿瘤周围的组织,从而导致转移的形成。实际上,已经发现Arf和Arl蛋白,以及它们的鸟嘌呤核苷酸交换因子(GEF)和GTPase激活蛋白(GAP)在不同的癌细胞类型和人类癌症中异常表达。在这里,我们回顾了支持Arf家族蛋白及其GEF和GAP参与癌症进展的当前证据,重点关注3种不同的机制:细胞间粘附,整联蛋白内化和再循环以及肌动蛋白细胞骨架重塑。

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