Zhang Hong-Ning, Feng Wei-Li, An Chun-Na, Li Wen-Guang
Department of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, China.
Department of Pharmacology, School of Basic Medical Sciences, Qinghai University, Xining 810001, China.
Oncotarget. 2017 Jul 1;8(40):67871-67877. doi: 10.18632/oncotarget.18909. eCollection 2017 Sep 15.
Selenium compounds have strong anti-tumor effects and are well-tolerated. We examined the anti-tumor effects of (NH)HSeMoVO·2HO (SeMoV, a heteropoly compound containing selenium. SeMoV inhibited proliferation in K562 cells with a half-maximal inhibitory concentration of 78.72±2.82 mg/L after 48 h and 24.94±0.88 mg/L after 72 h. Typical apoptotic morphologies were also observed in K562 cells treated with SeMoV, as were increased intracellular levels of Ca, Mg, H, and reactive oxygen species, and decreased mitochondrial membrane potential. In addition, SeMoV treatment triggered cytochrome C release and inhibited IκBα degradation and NF-κB translocation. experiments revealed that 5 or 10 mg/kg SeMoV inhibited the growth of sarcoma 180 and hepatoma 22 xenograft tumors. These results indicate that SeMoV inhibits tumor growth both and and induces apoptosis in K562 cells, possibly by inhibiting the NF-κB/IκBα pathway.
硒化合物具有很强的抗肿瘤作用,且耐受性良好。我们研究了(NH)HSeMoVO·2HO(硒钼钒,一种含硒的杂多化合物)的抗肿瘤作用。硒钼钒抑制K562细胞增殖,48小时后的半数最大抑制浓度为78.72±2.82毫克/升,72小时后为24.94±0.88毫克/升。在用硒钼钒处理的K562细胞中也观察到典型的凋亡形态,细胞内钙、镁、氢和活性氧水平升高,线粒体膜电位降低。此外,硒钼钒处理引发细胞色素C释放,抑制IκBα降解和NF-κB易位。实验表明,5或10毫克/千克的硒钼钒抑制肉瘤180和肝癌22异种移植肿瘤的生长。这些结果表明,硒钼钒在体内和体外均抑制肿瘤生长,并诱导K562细胞凋亡,可能是通过抑制NF-κB/IκBα途径实现的。