首页> 外文期刊>Current topics in nutraceutical research >The Structure-Activity Relationship and Molecular Mechanism of Anti-tumor Polysaccharide Isolated from Dendrobium Nobile Lindl.
【24h】

The Structure-Activity Relationship and Molecular Mechanism of Anti-tumor Polysaccharide Isolated from Dendrobium Nobile Lindl.

机译:抗肿瘤多糖与石斛中分离的抗肿瘤多糖的结构 - 活性关系及分子机制。

获取原文
获取原文并翻译 | 示例
       

摘要

In this study, structure-activity relationship and molecular mechanism of anti-tumor polysaccharide isolated from the stems of Dendrobium nobile Lindl. were investigated. The sulfate and enzymatic analysis were employed to modify polysaccharide DNP-W1A, a fraction of polysaccharide isolated from D. nobile. Nine sulfated derivative fragments (S1-S9) and three fragments after enzymatic digestion (PE1, PE2 and PE3) were obtained using chloro-sulfonic acid and enzymatic methods, respectively. The activities experiment demonstrated that S1-S9, PE1, PE2 and PE3 showed significant anti-tumor activities in a dose-dependent manner (P <0.05) in vitro. Annexin-FITC/PI results indicated that PE2 promoted the apoptosis of HepG2 cells at the highest rate of 19.3% compared with other fragments. Also, PE2 significantly increased the gene expression levels of Bax, Caspase-3 and Caspase-9 and suppressed the gene expression of Bcl-2 (P <0.01). Meanwhile, HepG2 cells treated with polysaccharide resulted in suppressed P-AKT expression, and PE2 induced the lowest protein level of P-AKT compared with other fragments. The results concluded that polysaccharide DNP-W1A and its derivatives induced HepG2 cells apoptosis by up-regulating the gene expressions of Bax, Bcl-2, Caspase-3 and Caspase-9 and inhibiting the PI3K/AKT signaling pathway.
机译:在该研究中,从石斛杆茎中分离的抗肿瘤多糖的结构 - 活性关系及分子机制。被调查了。使用硫酸盐和酶分析来修饰多糖DNP-W1A,从D. nobile中分离的多糖。使用氯 - 磺酸和酶法方法获得九个硫酸化衍生物片段(S1-S9)和三个片段,得到酶消化(PE1,PE2和PE3)。该活性实验证明S1-S9,PE1,PE2和PE3以剂量依赖性方式(P <0.05)呈现出显着的抗肿瘤活性。与其他碎片相比,Annexin-FITC / PI结果表明PE2以19.3%的最高速率促进了HepG2细胞的凋亡。此外,PE2显着增加了Bax,Caspase-3和Caspase-9的基因表达水平,并抑制了Bcl-2的基因表达(P <0.01)。同时,用多糖处理的HEPG2细胞导致抑制的P-AKT表达,与其他片段相比,PE2诱导p-akt的最低蛋白质水平。结果得出结论,多糖DNP-W1A及其衍生物通过上调Bax,Bcl-2,Caspase-3和Caspase-9的基因表达并抑制PI3K / AKT信号通路的基因表达,诱导HepG2细胞凋亡。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号