Stehn Justine R, Schevzov Galina, O'Neill Geraldine M, Gunning Peter W
Oncology Research Unit, The Children's Hospital at Westmead, Australia.
Curr Cancer Drug Targets. 2006 May;6(3):245-56. doi: 10.2174/156800906776842948.
The actin microfilament network is important in maintaining cell shape and function in eukaryotic cells. It has a multitude of roles in cellular processes such as cell adhesion, motility, cellular signalling, intracellular trafficking and cytokinesis. Alterations in the organisation of the cytoskeleton and changes in cellular morphology, motility and adhesiveness are characteristic features of transformed cancer cells. For this reason cytoskeletal microfilaments have become promising targets for chemotherapy. In contrast to the microtubules, which have been targeted successfully with anti-tumour drugs such as Taxol-like compounds and the Vinca alkaloids, very few actin targeting drugs have been characterised. To date, no actin targeting drugs have been used in clinical trials due to their severe cytotoxicity. One reason for this cytotoxicity is that drugs such as the cytochalasins and latrunculins disrupt actin microfilaments in both non-tumour and tumour cells. To circumvent this problem, actin filament populations need to be targeted more specifically. Not all actin filaments are the same and there is growing evidence that within a cell there are different populations of actin filaments which are spatially organised into distinct cellular compartments each with a unique function. The structure and function of the actin cytoskeleton is primarily regulated by the associated actin binding proteins. Tropomyosin is an intrinsic component of most actin filaments and over 40 isoforms have been identified in non-muscle cells. Tm isoforms are spatially segregated and current evidence suggests that they can specify the functional capacity of the actin microfilaments. Therefore the composition of these functionally distinct actin filaments may be important in determining their stability and function within the cell. If actin filament populations can be discriminated and targeted based on their tropomyosin composition then this becomes a powerful approach for anticancer therapy.
肌动蛋白微丝网络在维持真核细胞的细胞形状和功能方面很重要。它在细胞过程中发挥着多种作用,如细胞黏附、运动、细胞信号传导、细胞内运输和胞质分裂。细胞骨架组织的改变以及细胞形态、运动性和黏附性的变化是转化癌细胞的特征。因此,细胞骨架微丝已成为有前景的化疗靶点。与已被紫杉醇类化合物和长春花生物碱等抗肿瘤药物成功靶向的微管不同,很少有针对肌动蛋白的药物被鉴定出来。迄今为止,由于其严重的细胞毒性,尚无针对肌动蛋白的药物用于临床试验。这种细胞毒性的一个原因是,诸如细胞松弛素和拉春库林等药物会破坏非肿瘤细胞和肿瘤细胞中的肌动蛋白微丝。为了解决这个问题,需要更特异性地靶向肌动蛋白丝群体。并非所有肌动蛋白丝都是相同的,越来越多的证据表明,细胞内存在不同的肌动蛋白丝群体,它们在空间上组织成不同的细胞区室,每个区室都有独特的功能。肌动蛋白细胞骨架的结构和功能主要由相关的肌动蛋白结合蛋白调节。原肌球蛋白是大多数肌动蛋白丝的固有成分,在非肌肉细胞中已鉴定出40多种同工型。原肌球蛋白同工型在空间上是分离的,目前的证据表明它们可以指定肌动蛋白微丝的功能能力。因此,这些功能不同的肌动蛋白丝的组成可能对确定它们在细胞内的稳定性和功能很重要。如果能够根据原肌球蛋白组成区分并靶向肌动蛋白丝群体,那么这将成为一种强大的抗癌治疗方法。