Jung Michael, Grunberg Steven, Timblin Cynthia, Buder-Hoffman Sylke, Vacek Pamela, Taatjes Douglas J, Mossman Brooke T
Department of Pathology, University of Vermont College of Medicine, 89 Beaumont Avenue, Burlington, VT 05405, USA.
Histochem Cell Biol. 2004 Feb;121(2):115-21. doi: 10.1007/s00418-004-0618-8. Epub 2004 Jan 27.
Concurrent administration of paclitaxel and vinorelbine results in cytotoxicity in vivo and in vitro in a number of tumor cell lines, yet the mechanisms of enhanced cell killing are undefined. In studies here, we show that low concentrations (1 nM) of paclitaxel and vinorelbine in combination result in enhanced cell killing by apoptosis ( P<0.05) in the human lung adenocarcinoma cell line, A-549. In contrast, necrotic cell death and formation of multinucleated cells, which were significantly increased by paclitaxel ( P<0.05) alone, but not vinorelbine, were not increased synergistically by both drugs. Paclitaxel also caused microtubular disruption which was not observed with vinorelbine. These data provide further rationale for the combined use of paclitaxel and vinorelbine in clinical trials, and suggest that the cooperative effects of drugs on apoptosis are not mediated through similar disruptional effects on microtubules.
在多种肿瘤细胞系中,同时给予紫杉醇和长春瑞滨在体内和体外均会产生细胞毒性,但增强细胞杀伤作用的机制尚不清楚。在本研究中,我们发现低浓度(1 nM)的紫杉醇和长春瑞滨联合使用可导致人肺腺癌细胞系A-549通过凋亡增强细胞杀伤作用(P<0.05)。相比之下,坏死性细胞死亡和多核细胞的形成,仅紫杉醇(P<0.05)可使其显著增加,而长春瑞滨则无此作用,两种药物联合使用也不会使其协同增加。紫杉醇还会导致微管破坏,而长春瑞滨则不会。这些数据为紫杉醇和长春瑞滨在临床试验中的联合使用提供了进一步的理论依据,并表明药物对凋亡的协同作用并非通过对微管的类似破坏作用介导。