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癌症进展和转移中的肌动蛋白调节剂:从结构和功能到细胞骨架动力学。

Actin regulators in cancer progression and metastases: From structure and function to cytoskeletal dynamics.

机构信息

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.

出版信息

Int Rev Cell Mol Biol. 2020;356:131-196. doi: 10.1016/bs.ircmb.2020.05.006. Epub 2020 Jul 4.

Abstract

The cytoskeleton is a central factor contributing to various hallmarks of cancer. In recent years, there has been increasing evidence demonstrating the involvement of actin regulatory proteins in malignancy, and their dysregulation was shown to predict poor clinical prognosis. Although enhanced cytoskeletal activity is often associated with cancer progression, the expression of several inducers of actin polymerization is remarkably reduced in certain malignancies, and it is not completely clear how these changes promote tumorigenesis and metastases. The complexities involved in cytoskeletal induction of cancer progression therefore pose considerable difficulties for therapeutic intervention; it is not always clear which cytoskeletal regulator should be targeted in order to impede cancer progression, and whether this targeting may inadvertently enhance alternative invasive pathways which can aggravate tumor growth. The entire constellation of cytoskeletal machineries in eukaryotic cells are numerous and complex; the system is comprised of and regulated by hundreds of proteins, which could not be covered in a single review. Therefore, we will focus here on the actin cytoskeleton, which encompasses the biological machinery behind most of the key cellular functions altered in cancer, with specific emphasis on actin nucleating factors and nucleation-promoting factors. Finally, we discuss current therapeutic strategies for cancer which aim to target the cytoskeleton.

摘要

细胞骨架是导致癌症多种特征的核心因素。近年来,越来越多的证据表明肌动蛋白调节蛋白参与恶性肿瘤,其失调可预测不良的临床预后。尽管增强的细胞骨架活性通常与癌症进展相关,但在某些恶性肿瘤中,肌动蛋白聚合诱导物的表达显著降低,尚不清楚这些变化如何促进肿瘤发生和转移。细胞骨架诱导癌症进展的复杂性因此给治疗干预带来了相当大的困难;尚不清楚为了阻止癌症进展应该针对哪个细胞骨架调节剂,以及这种靶向是否可能无意中增强可以加重肿瘤生长的替代侵袭途径。真核细胞中细胞骨架的整个机器系统数量众多且复杂;该系统由数百种蛋白质组成并受其调控,这些内容无法在一篇综述中涵盖。因此,我们将在这里重点关注肌动蛋白细胞骨架,它包含了癌症中改变的大多数关键细胞功能背后的生物学机制,特别强调了肌动蛋白成核因子和成核促进因子。最后,我们讨论了目前针对癌症的旨在靶向细胞骨架的治疗策略。

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