Interactions between 14-3-3 Proteins and Actin Cytoskeleton and Its Regulation by microRNAs and Long Non-Coding RNAs in Cancer

J. Aseervatham
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Abstract

14-3-3s are a family of structurally similar proteins that bind to phosphoserine or phosphothreonine residues, forming the central signaling hub that coordinates or integrates various cellular functions, thereby controlling many pathways important in cancer, cell motility, cell death, cytoskeletal remodeling, neuro-degenerative disorders and many more. Their targets are present in all cellular compartments, and when they bind to proteins they alter their subcellular localization, stability, and molecular interactions with other proteins. Changes in environmental conditions that result in altered homeostasis trigger the interaction between 14-3-3 and other proteins to retrieve or rescue homeostasis. In circumstances where these regulatory proteins are dysregulated, it leads to pathological conditions. Therefore, deeper understanding is needed on how 14-3-3 proteins bind, and how these proteins are regulated or modified. This will help to detect disease in early stages or design inhibitors to block certain pathways. Recently, more research has been devoted to identifying the role of MicroRNAs, and long non-coding RNAs, which play an important role in regulating gene expression. Although there are many reviews on the role of 14-3-3 proteins in cancer, they do not provide a holistic view of the changes in the cell, which is the focus of this review. The unique feature of the review is that it not only focuses on how the 14-3-3 subunits associate and dissociate with their binding and regulatory proteins, but also includes the role of micro-RNAs and long non-coding RNAs and how they regulate 14-3-3 isoforms. The highlight of the review is that it focuses on the role of 14-3-3, actin, actin binding proteins and Rho GTPases in cancer, and how this complex is important for cell migration and invasion. Finally, the reader is provided with super-resolution high-clarity images of each subunit of the 14-3-3 protein family, further depicting their distribution in HeLa cells to illustrate their interactions in a cancer cell.
癌症14-3-3蛋白与肌动蛋白细胞骨架的相互作用及其微RNA和长非编码RNA的调控
14-3-3 -3是一个结构相似的蛋白家族,与磷丝氨酸或磷苏氨酸残基结合,形成协调或整合各种细胞功能的中央信号枢纽,从而控制癌症、细胞运动、细胞死亡、细胞骨架重塑、神经退行性疾病等许多重要途径。它们的靶标存在于所有的细胞区室中,当它们与蛋白质结合时,它们会改变其亚细胞定位、稳定性以及与其他蛋白质的分子相互作用。环境条件的变化导致体内平衡的改变,从而触发14-3-3与其他蛋白质之间的相互作用,以恢复或挽救体内平衡。在这些调节蛋白失调的情况下,它会导致病理状况。因此,需要对14-3-3蛋白如何结合以及这些蛋白是如何被调节或修饰的有更深入的了解。这将有助于在早期阶段发现疾病或设计抑制剂来阻断某些途径。近年来,人们对MicroRNAs和长链非编码rna的研究越来越多,它们在基因表达调控中起着重要的作用。虽然有很多关于14-3-3蛋白在癌症中的作用的综述,但它们并没有提供细胞变化的整体观点,这是本文的重点。该综述的独特之处在于,它不仅关注14-3-3亚基如何与它们的结合蛋白和调节蛋白结合和分离,而且还包括微rna和长链非编码rna的作用以及它们如何调节14-3-3亚型。本综述的重点是14-3-3、肌动蛋白、肌动蛋白结合蛋白和Rho gtpase在癌症中的作用,以及该复合物对细胞迁移和侵袭的重要作用。最后,为读者提供14-3-3蛋白家族每个亚基的超分辨率高清晰度图像,进一步描绘它们在HeLa细胞中的分布,以说明它们在癌细胞中的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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