Zhu Jiadan, Ji Zhiqiang, Wang Jing, Sun Ronghua, Zhang Xiang, Gao Yang, Sun Hongfang, Liu Yuanfang, Wang Zheng, Li Aidong, Ma Jie, Wang Tiancheng, Jia Guang, Gu Yiqun
Beijing National Laboratory for Molecular Sciences, Department of Chemical Biology, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P.R. China.
Small. 2008 Aug;4(8):1168-75. doi: 10.1002/smll.200701219.
The tumor-inhibitory effect of C60(OH)x was tested on the murine H22 hepatocarcinoma model. Doses of 0.2 and 1.0 mg kg(-1) body weight both showed significant antitumor activity with tumor inhibition rates of 31.9 and 38.4%, respectively, when mice were treated for 17 consecutive days. The damnification of liver was prominently reduced. Furthermore, histological examination indicated that an envelope of fibroblasts and lymphocytes was formed surrounding tumor tissues in the C60(OH)x-treated group, which inhibited the infiltration of tumor to the neighboring normal skeleton muscle tissues. To understand the antitumor mechanism, the immunomodulatory activity of C60(OH)x was investigated. The results indicate that C60(OH)x enhances the phagocytosis of peritoneal macrophages and elevates the activity of arginase and acid phosphatase in vivo. The tumor necrosis factor alpha production of C60(OH)x-treated macrophages also increases in vitro. These results suggest that C60(OH)x can enhance the innate immunity of tumor-bearing mice, and therefore inhibits growth of the tumor.
在小鼠H22肝癌模型上测试了C60(OH)x的抑瘤效果。当小鼠连续治疗17天时,0.2和1.0毫克/千克体重的剂量均显示出显著的抗肿瘤活性,肿瘤抑制率分别为31.9%和38.4%。肝脏损伤明显减轻。此外,组织学检查表明,在C60(OH)x治疗组中,肿瘤组织周围形成了一层由成纤维细胞和淋巴细胞组成的包膜,这抑制了肿瘤向邻近正常骨骼肌组织的浸润。为了解抗肿瘤机制,研究了C60(OH)x的免疫调节活性。结果表明,C60(OH)x可增强体内腹腔巨噬细胞的吞噬作用,并提高精氨酸酶和酸性磷酸酶的活性。体外实验中,经C60(OH)x处理的巨噬细胞产生肿瘤坏死因子α也增加。这些结果表明,C60(OH)x可增强荷瘤小鼠的固有免疫力,从而抑制肿瘤生长。