Anti-tumor Effect of Polysaccharides From Scutellaria Barbata D. Don on the 95-D Xenograft Model via Inhibition of the C-Met Pathway

被引:36
作者
Yang, Xiaokun [1 ,2 ]
Yang, Yadong [1 ]
Tang, Shuqian [1 ]
Tang, Hui [1 ]
Yang, Guihong [1 ]
Xu, Qiaoyu [1 ]
Wu, Jinjin [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Dept Dermatol, Chongqing 400042, Peoples R China
[2] Chengdu Mil Command Area, Gen Hosp, Dept Emergency, Chengdu 610083, Sichuan Provinc, Peoples R China
基金
中国国家自然科学基金;
关键词
polysaccharides Scutellaria barbata (PSB); c-Met; 95-D cell line; lung cancer; receptor tyrosine kinase; CELL LUNG-CANCER; PROTEIN-KINASE B; PHOSPHOINOSITIDE; 3-KINASE; PHOSPHATIDYLINOSITOL; CYTOSKELETAL FUNCTIONS; GROWTH; METASTASIS; EXPRESSION; MUTATIONS; RECEPTOR;
D O I
10.1254/jphs.13276FP
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polysaccharides isolated from Scutellaria barbata (PSB) have been reported to have anti-tumor effects. To investigate the underlying mechanism, a highly invasive, metastatic and phospho-c-Met overexpression lung carcinoma cell, 95-D cell line was used. The results showed that in vitro, PSB not only could inhibit the proliferation of 95-D cell line (IC50 = 35.2 mu g/mL), but also down-regulated the expression of phospho-c-Met and its downstream signaling molecules including phospho-Erk and phospho-Akt. In vivo, PSB inhibited tumor growth in the 95-D subcutaneous xenograft model in a dose-dependent manner; after once-daily intraperitoneal injection for 3 weeks, tumor growth inhibition T/C ratio for 100 and 200 mg/kg treatments was 42.72% and 13.6%, respectively. In the end of the in vivo study, tumor tissues were harvested for further evaluation of the phosphorylation level of c-Met, AKT, and ERK. Ex vivo results demonstrated that the phosphorylation of c-Met and its downstream signaling molecules were also significantly inhibited by PSB. Immunohistochemistry analysis showed dose-dependent inhibition of tumor cell proliferation (Ki67) and reduction of microvessel density (CD31). In summary, the results indicated that PSB exerted anti-tumor growth activity on human lung cancer 95-D in vitro and in vivo by directly regulating the c-Met signaling pathway and the anti-tumor effects were mainly based on its anti-proliferation and anti-angiogenesis action.
引用
收藏
页码:255 / 263
页数:9
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