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Transforming growth factor-β is required for vasculogenic mimicry formation in glioma cell line U251MG

机译:胶质瘤细胞系U251MG的血管生成模拟物形成需要转化生长因子-β

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摘要

Both vasculogenic mimicry (VM) and transforming growth factor-β (TGFβ) are positively correlated with malignancy in glioma. Accordingly, we supposed that TGFβ might be related with VM, and aimed to detect whether TGFβ could influence VM formation in two glioma cell lines U251MG and SHG44, which were different in malignancy. We found that the VM-positive U251MG had a significantly higher TGFβ expression than the VM-negative SHG44. Downregulating TGFβ in U251MG by RNAi technology resulted in a significantly impaired VM formation, which could be rescued by rhTGFβ. However, adding rhTGFβ could not induce VM in SHG44. To investigate the possible mechanism, we detected the changes of some VM-related genes including EphA2, VE-cadherin, MMP-2, MMP-9, MT1-MMP and LAMC2 by RT-PCR and found that MT1-MMP transcript was affected by TGFβ expression. Gelatin zymography showed a declined MMP-2 activity in the TGFβ-inhibited cells. Further studies showed that MT1-MMP inhibition impaired VM formation in U251MG. Moreover, TGFβ induced MT1-MMP expression and VM formation in a dose-dependent manner. These findings indicated us that TGFβ was required for VM formation in U251MG. MT1-MMP was correlated with TGFβ-induced VM formation. Thus, TGFβ might be a potential target for VM inhibition in glioma.
机译:血管生成模拟物(VM)和转化生长因子-β(TGFβ)与神经胶质瘤的恶性程度呈正相关。因此,我们认为TGFβ可能与VM有关,旨在检测TGFβ是否会影响恶性程度不同的两个神经胶质瘤细胞系U251MG和SHG44中VM的形成。我们发现,VM阳性U251MG具有比VM阴性SHG44高得多的TGFβ表达。 RNAi技术下调U251MG中的TGFβ导致VM形成明显受损,可通过rhTGFβ挽救。但是,添加rhTGFβ不能在SHG44中诱导VM。为了探讨可能的机制,我们通过RT-PCR检测了一些与VM有关的基因的变化,包括EphA2,VE-钙粘着蛋白,MMP-2,MMP-9,MT1-MMP和LAMC2,发现MT1-MMP转录本受到了影响。 TGFβ表达。明胶酶谱显示在TGFβ抑制的细胞中MMP-2活性下降。进一步的研究表明,MT1-MMP抑制会损害U251MG中的VM形成。此外,TGFβ以剂量依赖性方式诱导MT1-MMP表达和VM形成。这些发现表明,在U251MG中,VM形成需要TGFβ。 MT1-MMP与TGFβ诱导的VM形成有关。因此,TGFβ可能是神经胶质瘤中VM抑制的潜在靶标。

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