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alpha-Cyclodextrin Interacts Close to Vinblastine Site of Tubulin and Delivers Curcumin Preferentially to the Tubulin Surface of Cancer Cell

机译:α-环糊精相互作用接近微管蛋白长春碱的位置,并优先向癌细胞微管蛋白表面提供姜黄素。

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摘要

Tubulin is the key cytoskeleton component, which plays a crucial role in eukaryotic cell division. Many anticancer drugs have been developed targeting the tubulin surface. Recently, it has been shown that few polyhydroxy carbohydrates perturb tubulin polymerizatioo. Cyclodextrin (CD), a polyhydroxy carbohydrate, has been extensively used as the delivery vehicle for delivery of hydrophobic drugs to the cancer cell. However, interaction of CD with intracellular components has not been addressed before. In this Article, we have shown for the first time that alpha-CD interacts with tubulin close to the vinblastine site using molecular docking and Forster resonance energy transfer (FRET) experiment. In addition, we have shown that alpha-CD binds with intracellular tubulin/microtubule. It delivers a high amount of curcumin onto the cancer cell, which causes severe disruption of intracellular microtubules. Finally, we have shown that the inclusion complex of alpha-CD and curcumin (CCC), preferentially enters into the human lung cancer cell (A549) as compared to the normal lung fibroblast cell (WI38), causes apoptotic death, activates tumor suppressor protein (p53) and cyclin-dependent kinase inhibitor 1 (p21), and inhibits 3D spheroid growth of cancer cell.
机译:微管蛋白是关键的细胞骨架成分,在真核细胞分裂中起关键作用。已经开发了许多针对微管蛋白表面的抗癌药物。最近,已经显示出几乎没有多羟基碳水化合物干扰微管蛋白的聚合。环糊精(CD),一种多羟基碳水化合物,已被广泛用作将疏水性药物输送至癌细胞的输送媒介。但是,CD与细胞内组分的相互作用以前尚未解决。在本文中,我们首次使用分子对接和Forster共振能量转移(FRET)实验显示了α-CD与长春碱附近的微管蛋白相互作用。另外,我们已经证明α-CD与细胞内微管蛋白/微管结合。它向癌细胞输送大量姜黄素,这会严重破坏细胞内微管。最后,我们已经显示,与正常肺成纤维细胞(WI38)相比,α-CD和姜黄素(CCC)的包合复合物优先进入人肺癌细胞(A549),引起凋亡性死亡,激活肿瘤抑制蛋白(p53)和细胞周期蛋白依赖性激酶抑制剂1(p21),并抑制癌细胞的3D球形生长。

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