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A bibenzyl from Dendrobium ellipsophyllum inhibits migration in lung cancer cells

机译:石D石bi中的联苄抑制肺癌细胞的迁移

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Metastatic cancer cells have been shown to have aggressive behaviors accounting for the high incidence of chemotherapeutic failure and mortality. Because migration and invasion are crucial behaviors for cancer cell dissemination, promising compounds exhibiting potential antimigration effects are of interest for metastasis-based therapeutic approaches. This study aimed to evaluate the activity of a bibenzyl, 4,5,4'-trihydroxy-3,3'-dimethoxybibenzyl (TDB), isolated from Dendrobium ellipsophyllum Tang and Wang, in the suppression of migration in human lung cancer cells. TDB at nontoxic concentrations (1 and 5 A mu M) significantly inhibited the motility of lung cancer cells in scratch-wound assay. Chemotaxis-induced migration and invasion assays also revealed that the cell motility dramatically diminished in the cells treated with 1-5 A mu M TDB. Western blot analysis provided the underlying molecular mechanism, showing that TDB reduced such cell migration and invasion by decreasing migration-regulating proteins, including integrins alpha v, alpha 4, beta 1, beta 3 and beta 5, as well as downstream signaling proteins, such as activated focal adhesion kinase (pFAK), activated Ras-related C3 botulinum toxin substrate 1 (Rac1-GTP) and cell division control protein 42 (Cdc42). As the presence of cellular protrusion, called filopodia, has been indicated as a hallmark of migrating cells, we showed that the reduction of the mentioned proteins correlated well with the disappearance of filopodia. In summary, this study demonstrates the promising activity of TDB and its mechanism in the inhibition of lung cancer cell migration, which might be useful for encouraging the development of this compound for antimetastatic approaches.
机译:转移性癌细胞已被证明具有侵略性行为,导致化疗失败和死亡的发生率很高。因为迁移和侵袭是癌细胞扩散的关键行为,所以显示出潜在抗迁移作用的有希望的化合物对于基于转移的治疗方法很感兴趣。这项研究旨在评估从石D石Tang汤和王中分离出的联苄,4,5,4'-三羟基-3,3'-二甲氧基联苄(TDB)在抑制人肺癌细胞中的迁移活性。在刮伤试验中,无毒浓度(1和5 AμM)的TDB显着抑制肺癌细胞的运动。趋化性诱导的迁移和侵袭试验还显示,在用1-5 AμM TDB处理的细胞中,细胞运动显着降低。 Western印迹分析提供了潜在的分子机制,表明TDB通过减少迁移调节蛋白(包括整合素alpha v,alpha 4,beta 1,beta 3和beta 5以及下游信号传导蛋白,例如TGF-κB)减少了此类细胞迁移和侵袭。作为激活的粘着斑激酶(pFAK),激活的Ras相关C3肉毒杆菌毒素底物1(Rac1-GTP)和细胞分裂控制蛋白42(Cdc42)。由于已经表明存在称为丝状伪足的细胞突起,这是迁移细胞的标志,我们表明上述蛋白质的减少与丝状伪足的消失密切相关。总而言之,这项研究证明了TDB在抑制肺癌细胞迁移方面有希望的活性及其机制,这可能有助于鼓励这种化合物用于抗肿瘤方法的开发。

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