首页> 外文OA文献 >Cytotoxic Activity and Apoptosis Induction of Ethanolic Extract of Pericarps of Mangosteen (Garcinia mangostana Linn.) on WiDr Cells and Interaction Study of Alpha-mangosteen to IKK and VEGF Based on Molecular Docking
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Cytotoxic Activity and Apoptosis Induction of Ethanolic Extract of Pericarps of Mangosteen (Garcinia mangostana Linn.) on WiDr Cells and Interaction Study of Alpha-mangosteen to IKK and VEGF Based on Molecular Docking

机译:基于分子对接的山竹(Garcinia Mangostana LiNn,Garcinia Mangostana LiNN脑膜脑膜炎术乙醇提取物的细胞毒性活性和凋亡诱导α-山上α-山上血小板和VEGF的相互作用研究

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摘要

One of the compounds found efficacious as an anti-proliferative on colon cancer is alpha-mangosteen, a xanthon compound that is abundant in pericarp of mangosteen. This study focused to evaluate anticancer activity of the ethanolic extract of pericarp of mangosteen (Garcinia mangostana Linn.) on WiDr colon cancer cells and to observe the affinity of alpha-mangosteen in inhibiting IKK and VEGF. Cytotoxic effect was tested by MTT assay and apoptosis induction was evaluated by double staining method on WiDr colon cancer cells, while interaction between alpha-mangosteen to the receptors was measured by molecular docking. The ethanolic extract was proven to have cytotoxic activity against WiDr colon cancer cells with IC50 of 25 µg/mL. In addition, the observation of apoptosis induction by double-staining method showed that apoptosis associated the cytotoxic effect of ethanolic extract of pericarp of mangosteen (EPM) on WiDr colon cancer cells. Molecular docking showed that active compounds in pericarp of mangosteen could compete with the native ligand of VEGF because the docking score of alpha-mangosteen was almost equal with native ligand. From these results we could be concluded that the cytotoxic effect of EPM to WiDr cells was mediated by cell apoptosis. This extract was potential to be developed as chemopreventive agent.Keywords : Garcinia mangostana Linn., cytotoxic effect, apoptosis, WiDr cell, molecular docking
机译:其中一种化合物在结肠癌上抗增殖是抗增殖的是α-山宫,在山竹果皮中丰富的Xanthon化合物。本研究重点是评估山竹癌(Garcinia Mangostana Linn.)乙醇提取物对WIDR结肠癌细胞的抗癌活性,并观察α-山底膜在抑制IKK和VEGF中的亲和力。通过MTT测定测试细胞毒性效应,通过对WIDR结肠癌细胞的双染色方法评估细胞凋亡诱导,同时通过分子对接测量对受体的α-山上与受体之间的相互作用。被证明的乙醇提取物对WIDR结肠癌细胞的细胞毒性活性具有25μg/ mL的IC50。此外,双染色方法观察细胞凋亡诱导表明,凋亡与血小板术(EPM)乙醇提取物对WIDR结肠癌细胞的乙醇提取物的细胞毒性作用。分子对接表明,山竹果皮中的活性化合物可以与VEGF的天然配体竞争,因为α-山竹的对接得分几乎与天然配体几乎相等。从这些结果可以得出结论,EPM对WIDR细胞的细胞毒性作用被细胞凋亡介导。这种提取物潜力是开发为化学预防症的潜力。(Cytoxic yancorance),细胞毒性效果,细胞凋亡,WIDR细胞,分子对接

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