Lai S R, Castello S A, Robinson A C, Koehler J W
Department of Clinical Sciences, Auburn University College of Veterinary Medicine, Auburn, AL, USA.
Undergraduate Honors College, Auburn University, Auburn, AL, USA.
Vet Comp Oncol. 2017 Dec;15(4):1445-1454. doi: 10.1111/vco.12288. Epub 2017 Jan 12.
Benzimidazole anthelmintics have reported anti-neoplastic effects both in vitro and in vivo. The purpose of this study was to evaluate the in vitro chemosensitivity of three canine glioma cell lines to mebendazole and fenbendazole. The mean inhibitory concentration (IC ) (±SD) obtained from performing the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay after treating J3T, G06-A, and SDT-3G cells for 72 h with mebendazole were 0.030 ± 0.003, 0.080 ± 0.015 and 0.030 ± 0.006 μM respectively, while those for fenbendazole were 0.550 ± 0.015, 1.530 ± 0.159 and 0.690 ± 0.095 μM; treatment of primary canine fibroblasts for 72 h at IC showed no significant effect. Immunofluorescence studies showed disruption of tubulin after treatment. Mebendazole and fenbendazole are cytotoxic in canine glioma cell lines in vitro and may be good candidates for treatment of canine gliomas. Further in vivo studies are required.
苯并咪唑类驱虫药在体外和体内均有抗肿瘤作用的报道。本研究的目的是评估三种犬胶质瘤细胞系对甲苯达唑和芬苯达唑的体外化学敏感性。在用甲苯达唑处理J3T、G06 - A和SDT - 3G细胞72小时后,通过MTT [3 - (4,5 - 二甲基噻唑 - 2 - 基)-2,5 - 二苯基四氮唑溴盐] 试验获得的平均抑制浓度 (IC) (±标准差) 分别为0.030±0.003、0.080±0.015和0.030±0.006 μM,而芬苯达唑的平均抑制浓度分别为0.550±0.015、1.530±0.159和0.690±0.095 μM;在IC浓度下处理原代犬成纤维细胞72小时未显示出显著影响。免疫荧光研究显示处理后微管蛋白被破坏。甲苯达唑和芬苯达唑在体外对犬胶质瘤细胞系具有细胞毒性,可能是治疗犬胶质瘤的良好候选药物。还需要进一步的体内研究。