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MEK/ERK pathway is positively involved in hypoxia-induced vasculogenic mimicry formation in hepatocellular carcinoma which is regulated negatively by protein kinase A

机译:MEK / ERK通路积极参与缺氧诱导的肝细胞癌血管生成拟态的形成,其受蛋白激酶A负调控

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The aim of present investigation is to explore the molecular mechanisms of vasculogenic mimicry (VM) induced by hypoxia. Hepatocellular carcinoma cell lines were treated with CoCl2, and the VM-related parameters were assayed by real-time qPCR, Western blotting and immunofluorescence. Matrigel tube structure was also detected. We demonstrated that the expression of pMEK, MEK, pERK1/2 and ERK1/2 had a positive correlation with VM induced by hypoxia in MHCC97H while HepG2 signified VM under normoxia condition. PD98059 was negatively while epidermal growth factor positively participated in the increased tubes and area of VM. At the meaning time, the increased VM-related genes VE-cadherin, MMP2, MMP9, EphA2 and LAMC2 in hypoxia group were down-regulated by PD98059 in a dose-dependent manner. Furthermore, we elucidated that PKA, but not PKC, mediated the MEK/ERK pathway in a negative manner in VM. In conclusion, MEK/ERK pathway is positively involved in VM in hepatocellular carcinoma cell line, which was mediated by PKA negatively.
机译:本研究的目的是探讨缺氧诱导的血管生成拟态(VM)的分子机制。用CoCl2处理肝癌细胞系,并通过实时qPCR,Western印迹和免疫荧光测定VM相关参数。还检测到基质胶管结构。我们证明,在正常氧条件下,MHCC97H中pMEK,MEK,pERK1 / 2和ERK1 / 2的表达与缺氧诱导的VM呈正相关,而HepG2则表示VM处于正常状态。 PD98059阴性,而表皮生长因子阳性参与了VM的增加管和面积。此时,缺氧组增加的VM相关基因VE-cadherin,MMP2,MMP9,EphA2和LAMC2被PD98059以剂量依赖性方式下调。此外,我们阐明了PKA,而不是PKC,在VM中以负面的方式介导了MEK / ERK途径。综上所述,MEK / ERK通路与肝癌细胞的VM呈正相关,而PKA负介导。

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