Steinestel Konrad, Wardelmann Eva, Hartmann Wolfgang, Grünewald Inga
Gerhard Domagk Institute of Pathology, University Hospital Münster, 48149 Münster, Germany.
Gastroenterol Res Pract. 2015;2015:930157. doi: 10.1155/2015/930157. Epub 2015 Aug 4.
Reorganization of the actin cytoskeleton underlies cell migration in a wide variety of physiological and pathological processes, such as embryonic development, wound healing, and tumor cell invasion. It has been shown that actin assembly and disassembly are precisely regulated by intracellular signaling cascades that respond to changes in the cell microenvironment, ligand binding to surface receptors, or oncogenic transformation of the cell. Actin-nucleating and actin-depolymerizing (ANFs/ADFs) and nucleation-promoting factors (NPFs) regulate cytoskeletal dynamics at the leading edge of migrating cells, thereby modulating cell shape; these proteins facilitate cellular movement and mediate degradation of the surrounding extracellular matrix by secretion of lytic proteases, thus eliminating barriers for tumor cell invasion. Accordingly, expression and activity of these actin-binding proteins have been linked to enhanced metastasis and poor prognosis in a variety of malignancies. In this review, we will summarize what is known about expression patterns and the functional role of actin regulators in gastrointestinal tumors and evaluate first pharmacological approaches to prevent invasion and metastatic dissemination of malignant cells.
肌动蛋白细胞骨架的重组是多种生理和病理过程中细胞迁移的基础,如胚胎发育、伤口愈合和肿瘤细胞侵袭。研究表明,肌动蛋白的组装和解聚受细胞内信号级联精确调控,这些信号级联对细胞微环境变化、配体与表面受体结合或细胞的致癌转化作出反应。肌动蛋白成核和肌动蛋白解聚因子(ANFs/ADFs)以及成核促进因子(NPFs)调节迁移细胞前缘的细胞骨架动力学,从而调节细胞形状;这些蛋白质促进细胞运动,并通过分泌溶蛋白性蛋白酶介导周围细胞外基质的降解,从而消除肿瘤细胞侵袭的障碍。因此,这些肌动蛋白结合蛋白的表达和活性与多种恶性肿瘤的转移增强和预后不良有关。在这篇综述中,我们将总结关于肌动蛋白调节剂在胃肠道肿瘤中的表达模式和功能作用的已知信息,并评估预防恶性细胞侵袭和转移扩散的首批药理学方法。