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首页> 外文期刊>Journal of pharmacological sciences. >Anti-tumor effect of polysaccharides from Scutellaria barbata d. don on the 95-D xenograft model via inhibition of the C-met pathway
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Anti-tumor effect of polysaccharides from Scutellaria barbata d. don on the 95-D xenograft model via inhibition of the C-met pathway

机译:半枝莲多糖的抗肿瘤作用d。通过抑制C-met途径在95-D异种移植模型上进行穿刺

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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 μg/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.
机译:据报道,从半枝莲(PSB)分离出的多糖具有抗肿瘤作用。为了研究潜在的机制,使用了高度侵袭性,转移性和磷酸化c-Met过表达的肺癌细胞95-D细胞系。结果表明,在体外,PSB不仅可以抑制95-D细胞系的增殖(IC50 = 35.2μg/ mL),而且还可以下调磷酸化c-Met及其下游信号分子(包括磷酸化磷酸化)的表达。 Erk和磷酸化Akt。在体内,PSB以剂量依赖性方式抑制95-D皮下异种移植模型中的肿瘤生长。每天一次腹膜内注射3周后,100和200 mg / kg治疗的肿瘤生长抑制T / C比分别为42.72%和13.6%。在体内研究结束时,收获肿瘤组织用于进一步评估c-Met,AKT和ERK的磷酸化水平。离体结果表明,c-Met及其下游信号分子的磷酸化也受到PSB的显着抑制。免疫组织化学分析显示剂量依赖性抑制肿瘤细胞增殖(Ki67)和降低微血管密度(CD31)。总之,结果表明,PSB通过直接调节c-Met信号通路在体内和体外对人肺癌95-D发挥抗肿瘤作用,其抗肿瘤作用主要是基于其抗增殖和抗癌作用。抗血管生成作用。

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