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Oldhamianoside II, a new triterpenoid saponin, prevents tumor growth via inducing cell apoptosis and inhibiting angiogenesis

机译:一种新的三萜皂苷Oldhamianoside II,可通过诱导细胞凋亡和抑制血管生成来防止肿瘤生长

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Oldhamianoside II is a new triterpenoid saponin that was isolated from the roots of Gypsophila oldhamiana. The present study aims to investigate the potential inhibitory activity of oldhamianoside II on tumor growth using an S180 tumor implantation mouse model. Oldhamianoside II at doses of 5.0 and 10.0 mg/kg was given with intraperitoneal injection for 10 days following subcutaneous inoculation of S180 tumor cells in anterior flank of mice. The tumor growth, the cell apoptosis, the microvessel density (MVD) in S180 tumors, the tumor cell viability, the tubular formation in vitro, and migration of tumor cells were examined. The expression of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and cyclooxygenase-2 (COX-2) was determined to analyze the associated mechanisms. The results showed that oldhamianoside II potently inhibited tumor cell viability in vitro. In addition, oldhamianoside II delayed tumor growth in anterior flank, induced S180 cell apoptosis, and reduced the MVD. Oldhamianoside II was also demonstrated to decrease the number of tubular structure and vessel formation in HUVEC cultures and chick embryo chorioallantoic membrane (CAM) model, respectively. Further study indicated that oldhamianoside II reduced the expression of VEGF, bFGF, and COX-2 in tumor sections. Moreover, oldhamianoside II inhibited the activity of migration and penetration to Matrigel of SGC7901 tumor cells in scratch wound and transwell chamber. In conclusion, our work defines oldhamianoside II, a new triterpenoid saponin, as a novel compound that can effectively inhibit S180 tumor growth, induce tumor cell apoptosis, prevent tumor angiogenesis, and inhibit cancer cell migration, suggesting that oldhamianoside II is a potential drug candidate for the treatment of cancer and for the prevention of metastasis.
机译:Oldhamianoside II是一种新的三萜皂苷,是从满天星满天星的根中分离出来的。本研究旨在研究使用S180肿瘤植入小鼠模型的Oldhamianoside II对肿瘤生长的潜在抑制活性。皮下接种小鼠前侧面的S180肿瘤细胞后,以5.0和10.0 mg / kg的剂量将Oldhamianoside II腹膜内注射10天。检查S180肿瘤的肿瘤生长,细胞凋亡,微血管密度(MVD),肿瘤细胞活力,体外小管形成以及肿瘤细胞的迁移。确定血管内皮生长因子(VEGF),碱性成纤维细胞生长因子(bFGF)和环氧合酶2(COX-2)的表达以分析相关机制。结果表明,Oldhamianoside II在体外可有效抑制肿瘤细胞的活力。此外,Oldhamianoside II延迟了前牙的肿瘤生长,诱导了S180细胞凋亡,并降低了MVD。还证明了Oldhamianoside II可以减少HUVEC培养物和鸡胚绒膜尿囊膜(CAM)模型中的管状结构数量和血管形成。进一步的研究表明,Oldhamianoside II降低了肿瘤切片中VEGF,bFGF和COX-2的表达。此外,Oldhamianoside II抑制了SGC7901肿瘤细胞在刮擦伤口和转运孔中的迁移和向Matrigel的渗透活性。总而言之,我们的工作将新的三萜皂苷类新品三滨皂苷II定义为可以有效抑制S180肿瘤生长,诱导肿瘤细胞凋亡,预防肿瘤血管生成和抑制癌细胞迁移的新型化合物,这表明三ham苷II是潜在的候选药物。用于治疗癌症和预防转移。

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