Wang Xiaomin, Guo Zhanyun
Institute of Protein Research, College of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.
Cell Biochem Biophys. 2015 Nov;73(2):389-392. doi: 10.1007/s12013-015-0634-4.
Malignant gliomas are rarely curable malignant tumors in the central nervous system. Chlorotoxin (CTX) is a peptide derived from scorpion venom, which can selectively target malignant gliomas. Onconase (Onc) is a small cytotoxic ribonuclease derived from frogspawn that exhibits cytotoxicity against some tumor cells. In the present study, we found that CTX-conjugated Onc (CTX-Onc) shows better anti-tumor effect than the physical mixture of CTX and Onc (CTX + Onc) on the nude mice carrying subcutaneous glioblastoma cell-derived tumor. However, CTX-Onc does not show dose-dependent anti-tumor effect. In addition, apoptosis in tumor tissue does not show significant difference between the treatment groups. Our results confirmed that CTX-Onc has better anti-tumor effect than CTX + Onc and suggest that it can be potentially used for glioma therapy.
恶性胶质瘤是中枢神经系统中难以治愈的恶性肿瘤。氯毒素(CTX)是一种源自蝎毒的肽,它能够选择性地靶向恶性胶质瘤。昂卡酶(Onc)是一种源自蛙卵的小型细胞毒性核糖核酸酶,对某些肿瘤细胞具有细胞毒性。在本研究中,我们发现CTX偶联昂卡酶(CTX-Onc)对携带皮下胶质母细胞瘤细胞衍生肿瘤的裸鼠显示出比CTX与昂卡酶的物理混合物(CTX + Onc)更好的抗肿瘤效果。然而,CTX-Onc并未表现出剂量依赖性抗肿瘤效果。此外,各治疗组之间肿瘤组织中的细胞凋亡没有显著差异。我们的结果证实,CTX-Onc比CTX + Onc具有更好的抗肿瘤效果,并表明它有可能用于胶质瘤治疗。