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细胞骨架作为抗肿瘤药物氯尼达明的亚细胞靶点。

The cytoskeleton as a subcellular target of the antineoplastic drug lonidamine.

作者信息

Malorni W, Meschini S, Matarrese P, Arancia G

机构信息

Department of Ultrastructures, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Anticancer Res. 1992 Nov-Dec;12(6B):2037-45.

PMID:1295447
Abstract

Lonidamine (LND), a dichlorinated derivative of indazole-3-carboxylic acid, has proved to exert a powerful antiproliferative effect and to impair the energy metabolism of normal and neoplastic cells. A target effect of the drug on the cell membrane structure was hypothesized. Thus, in order to elucidate better the mechanism of action of LND, the drug effects on the cell surface as well as on main cytoskeletal elements, i.e. actin microfilaments, microtubules and intermediate filaments, were investigated. In particular, an immunocytochemical and ultrastructural study was performed using two different cell lines: epithelial squamous carcinoma (A431) and melanoma (M14) cells. Treatment with 0.8 mM LND for 8 hr induced a remarkable rearrangement of the F-actin molecules with the disappearance of the stress fibers. As far as microtubules are concerned, formation of perinuclear patches of tubulin were detected after LND treatment. Intermediate filaments appeared to be differently affected by LND in the two cell types. Such changes were detected as an early phenomenon and the extent of the effects observed was positively related to the cell surface alterations and to the loss of cell viability, suggesting that the cytoskeletal elements might represent an additional target in the mechanisms of cytotoxic action of LND.

摘要

氯尼达明(LND)是吲唑 - 3 - 羧酸的二氯衍生物,已被证明具有强大的抗增殖作用,并损害正常细胞和肿瘤细胞的能量代谢。推测该药物对细胞膜结构有靶向作用。因此,为了更好地阐明LND的作用机制,研究了该药物对细胞表面以及主要细胞骨架成分,即肌动蛋白微丝、微管和中间丝的影响。特别是,使用两种不同的细胞系进行了免疫细胞化学和超微结构研究:上皮鳞状癌(A431)和黑色素瘤(M14)细胞。用0.8 mM LND处理8小时导致F - 肌动蛋白分子显著重排,应力纤维消失。就微管而言,LND处理后检测到微管蛋白在核周形成斑块。在两种细胞类型中,中间丝受LND的影响似乎不同。这些变化被检测为早期现象,观察到的影响程度与细胞表面改变和细胞活力丧失呈正相关,表明细胞骨架成分可能是LND细胞毒性作用机制中的另一个靶点。

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