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Dynamic MR imaging for functional vascularization depends on tissue factor signaling in glioblastoma

机译:功能性血管化的动态MR成像取决于胶质母细胞瘤中的组织因子信号

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Glomeruloid vascular proliferation (GVP) is a diagnostic hallmark and links to aggressive behavior, therapy resistance and poor prognosis in glioblastoma (GBM). It lacks clinical approaches to predict and monitor its formation and dynamic change. Yet the mechanism of GVPs also remains largely unknown. Using an in situ GBM xenograft mouse model, combined clinical MRI images of pre-surgery tumor and pathological investigation, we demonstrated that the inhibition of tissue factor (TF) decreased GVPs in Mouse GBM xenograft model. TF shRNA reduced microvascular area and diameter, other than bevacizumab. TF dominantly functions via PAR2/HB-EGF-dependent activation under hypoxia in endothelial cells (ECs), resulting in a reduction of GVPs and cancer cells invasion. TF expression strongly correlated to GVPs and microvascular area (MVA) in GBM specimens from 56 patients, which could be quantitatively evaluated in an advanced MRI images system in 33 GBM patients. This study presented an approach to assess GVPs that could be served as a MRI imaging biomarker in GBM and uncovered a molecular mechanism of GVPs.
机译:肾小球血管增殖(GVP)是一种诊断标志和与脊髓母细胞瘤(GBM)中的侵略性行为,治疗性和预后不良的联系。它缺乏预测和监测其形成和动态变化的临床方法。然而,GVPS的机制仍然很大程度上是未知的。使用原位GBM异种移植鼠标模型,组合临床MRI图像前手术前肿瘤和病理调查,我们证明了组织因子(TF)的抑制在小鼠GBM异种移植模型中的GVPS降低。 TF shRNA减少微血管区域和直径,除贝伐单抗之外。 TF通过PAR2 / HB-EGF依赖性活化在内皮细胞(ECS)下依赖于PAR2 / HB-EGF依赖性激活,导致GVPS和癌细胞侵袭的降低。 TF表达与56名患者的GBM标本中GBM标本中的GVP和微血管区域(MVA)强烈相关,可以在33杆GBM患者的高级MRI图像系统中定量评估。该研究提出了一种评估GVPS的方法,其可以用作GBM中的MRI成像生物标志物,并揭示GVPS的分子机制。

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