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Hypoxia mediated up-regulation of DLL4 in A549 cells and its influence on migration of endothelial cells

机译:缺氧在A549细胞中介导DLL4的上调及其对内皮细胞迁移的影响

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More people died from lung cancer than any other type of cancer in China. Recently, studies have shown that antiangiogenesis is a promising therapy strategy in lung cancer treatment. Delta-like ligand 4 (DLL4), is one of the highly conserved notch ligand which participates in the process of vascular formation. Therefore, more and more attention had paid to this ligand as a cancer therapeutic target. However, the underlying evidence is still largely absent. In the present study, we intend to elucidate the effect of tumor-derived DLL4 on the migration of endothelial cells. Using cobalt chloride CoCl_2 to mimic the hypoxia condition in lung cancer cell line A549 in vitro and explore the expression of DLL4 in A549 cells. We also observe the migration of endothelial cells in the condition of CoCl_2 treated cancer cell culture supernatant.
机译:更多人从肺癌中死亡而不是中国任何其他类型的癌症。最近,研究表明,抗脑发生是肺癌治疗中有前途的治疗策略。三角洲配体4(DLL4)是高度保守的凹口配体之一,其参与血管形成过程。因此,越来越多的注意力为该配体作为癌症治疗靶标。但是,潜在的证据仍然很大程度上。在本研究中,我们打算阐明肿瘤衍生的DLL4对内皮细胞迁移的影响。使用氯化钴COCl_2在体外模拟肺癌细胞系A549中的缺氧条件,探讨A549细胞DLL4的表达。我们还观察到内皮细胞在COCl_2处理的癌细胞培养上清液中的迁移。

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