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钙通道阻滞剂对肿瘤细胞的治疗会诱导细胞骨架改变、整合素αIIbβ3的迁移以及肿瘤细胞诱导的血小板聚集。

Calcium channel blocker treatment of tumor cells induces alterations in the cytoskeleton, mobility of the integrin alpha IIb beta 3 and tumor-cell-induced platelet aggregation.

作者信息

Timar J, Chopra H, Rong X, Hatfield J S, Fligiel S E, Onoda J M, Taylor J D, Honn K V

机构信息

Department of Radiation Oncology, Wayne State University, Detroit, MI 48202.

出版信息

J Cancer Res Clin Oncol. 1992;118(6):425-34. doi: 10.1007/BF01629425.

Abstract

Calcium channel blockers of the phenylalkylamine (i.e. verapamil), benzothiazepine (i.e. diltiazem) and dihydropyridine (i.e. nifedipine) classes were evaluated for effects on the tumor cell/platelet interactions using Walker 256 carcinosarcoma cells (W256 cells). When W256 cells were pretreated for 15 min with channel blockers at concentrations of 50-200 microM, macroscopic tumor-cell-induced platelet aggregation was inhibited (order of potency; nifedipine greater than diltiazem much greater than verapamil). However, ultrastructural analysis revealed limited, focal platelet aggregates associated with tumor cell plasma membranes of verapamil- and diltiazem-treated cells. There was no evidence of platelet activation or platelet association with the tumor cell membrane in cells pretreated with nifedipine. Walker 256 cells possess the intergrin alpha IIb beta 3. Tumor cell alpha IIb beta 3 was shown to mediate tumor cell/platelet interactions in vitro [Chopra et al. (1988) Cancer Res. 48:3787]. Patching and capping of surface alpha IIb beta 3 were inhibited by nifedipine greater than diltiazem much greater than verapamil. The degree of inhibition of alpha IIb beta 3 receptor mobility parallels the inhibition of tumor-cell-induced platelet aggregation. W256 cells are characterized by a well-developed microfilament and intermediate filament network and by the absence of a distinct microtubular network. Calcium channel blockers had no effect on the low polymerization level of tubulin. However, they induced rearrangement of microfilament stress fibers. Intermediate filaments were also rearranged but to varying degrees. The order of effectiveness for alteration of intermediate filament organization was nifedipine greater than diltiazem while verapamil was ineffective. We propose that the previously reported inhibition of tumor cell/platelet interaction and tumor cell metastasis by calcium channel blockers [Honn et al. (1984) Clin Exp Metastasis 1:61] is due not only to the effects of the Ca2+ channel blockers on platelets, but also to their effect on the tumor cell cytoskeleton resulting in an inhibition of the mobility and function of the alpha IIb beta 3 receptor.

摘要

使用Walker 256癌肉瘤细胞(W256细胞)评估了苯烷基胺类(即维拉帕米)、苯并硫氮䓬类(即地尔硫䓬)和二氢吡啶类(即硝苯地平)的钙通道阻滞剂对肿瘤细胞/血小板相互作用的影响。当W256细胞用浓度为50 - 200微摩尔的通道阻滞剂预处理15分钟时,宏观的肿瘤细胞诱导的血小板聚集受到抑制(效力顺序为;硝苯地平大于地尔硫䓬远大于维拉帕米)。然而,超微结构分析显示,与维拉帕米和地尔硫䓬处理的细胞的肿瘤细胞质膜相关的血小板聚集有限且呈局灶性。在用硝苯地平预处理的细胞中,没有血小板活化或血小板与肿瘤细胞膜结合的证据。Walker 256细胞具有整合素αIIbβ3。肿瘤细胞αIIbβ3在体外被证明介导肿瘤细胞/血小板相互作用[Chopra等人(1988年)《癌症研究》48:3787]。表面αIIbβ3的斑块形成和帽化被硝苯地平抑制的程度大于地尔硫䓬远大于维拉帕米。αIIbβ3受体流动性的抑制程度与肿瘤细胞诱导的血小板聚集的抑制程度平行。W256细胞的特征是具有发达的微丝和中间丝网络,且没有明显的微管网络。钙通道阻滞剂对微管蛋白的低聚合水平没有影响。然而,它们诱导了微丝应力纤维的重排。中间丝也发生了重排,但程度不同。中间丝组织改变的效力顺序为硝苯地平大于地尔硫䓬,而维拉帕米无效。我们提出,先前报道的钙通道阻滞剂对肿瘤细胞/血小板相互作用和肿瘤细胞转移的抑制作用[Honn等人(1984年)《临床与实验转移》1:61]不仅归因于Ca2+通道阻滞剂对血小板的作用,还归因于它们对肿瘤细胞细胞骨架的作用,从而导致αIIbβ3受体的流动性和功能受到抑制。

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