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首页> 外文期刊>Scientific reports. >Exosomes released from pancreatic cancer cells enhance angiogenic activities via dynamin-dependent endocytosis in endothelial cells in vitro
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Exosomes released from pancreatic cancer cells enhance angiogenic activities via dynamin-dependent endocytosis in endothelial cells in vitro

机译:胰腺癌细胞释放的外泌体通过动力蛋白依赖性内吞作用在体外内皮细胞中增强血管生成活性

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摘要

Pancreatic cancer has the lowest 5 year survival rate among all cancers. Several extracellular factors are involved in the development and metastasis of pancreatic cancer to distant organs. Exosomes are lipid-bilayer, membrane-enclosed nanoparticles that are recognised as important mediators of cell-to-cell communications. However, the role of exosomes released from pancreatic cancer cells in tumour micro-environment remains unknown. Here, we show that exosomes released from pancreatic cancer PK-45H cells activate various gene expressions in human umbilical vein endothelial cells (HUVECs) by in vitro analyses. In addition, these exosomes released from PK-45H cells promote phosphorylation of Akt and ERK1/2 signalling pathway molecules and tube formation via dynamin-dependent endocytosis in HUVECs. Our findings suggested that exosomes released from pancreatic cancer cells may act as a novel angiogenesis promoter.
机译:在所有癌症中,胰腺癌的5年生存率最低。几种细胞外因子参与胰腺癌向远处器官的发展和转移。外泌体是脂质双层,膜包裹的纳米颗粒,被认为是细胞间通讯的重要介质。然而,从胰腺癌细胞释放的外来体在肿瘤微环境中的作用仍然未知。在这里,我们显示从胰腺癌PK-45H细胞释放的外泌体通过体外分析激活人脐静脉内皮细胞(HUVEC)中的各种基因表达。此外,这些从PK-45H细胞释放的外泌体通过HUVEC中的动力蛋白依赖性内吞作用促进Akt和ERK1 / 2信号通路分子的磷酸化以及管的形成。我们的发现表明,从胰腺癌细胞释放的外泌体可能充当新型血管生成促进剂。

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