Sawanyawisuth Kanlayanee, Williamson Tara, Wongkham Sopit, Riggins Gregory J
Southeast Asian J Trop Med Public Health. 2014 Nov;45(6):1264-70.
Mebendazole (MBZ) is an anthelmintic drug which inhibits tubulin polymerization and eventually causes apoptosis in target organisms. Antitumor activity of MBZ has been reported in various cancers. The aim of this study was to investigate the effect of MBZ on cholangiocarcinoma (CCA) cells in vitro and in vivo. MBZ reduced cell proliferation in the KKU-M213 cell line associated with a remarkable enhancement of caspase-3 gene expression and enzyme activity. Oral administration of MBZ slightly reduced the growth rate of subcutaneously xeno-grafted KKU-M213 in nude mice. The TUNEL assay showed an increase of apoptotic cell numbers in the xenograft tumor tissue of MBZ-treated mice. The data obtained in this study suggested that MBZ can suppress CCA cell proliferation via caspase-3 activated apoptosis. Further investigation of the antitumor effects of MBZ might support the use of MBZ as an alternative drug for CCA treatment.
甲苯咪唑(MBZ)是一种驱虫药,它能抑制微管蛋白聚合,最终导致靶生物体凋亡。MBZ在多种癌症中均有抗肿瘤活性的报道。本研究的目的是在体外和体内研究MBZ对胆管癌(CCA)细胞的影响。MBZ降低了KKU-M213细胞系中的细胞增殖,这与caspase-3基因表达和酶活性的显著增强有关。口服MBZ可略微降低裸鼠皮下异种移植的KKU-M213的生长速率。TUNEL检测显示,MBZ处理的小鼠异种移植肿瘤组织中的凋亡细胞数量增加。本研究获得的数据表明,MBZ可通过caspase-3激活的凋亡抑制CCA细胞增殖。对MBZ抗肿瘤作用的进一步研究可能支持将MBZ用作CCA治疗的替代药物。