首页> 美国卫生研究院文献>Frontiers in Neuroscience >Enhanced γ-Glutamyltranspeptidase Imaging That Unravels the Glioma Recurrence in Post-radio/Chemotherapy Mixtures for Precise Pathology via Enzyme-Triggered Fluorescent Probe
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Enhanced γ-Glutamyltranspeptidase Imaging That Unravels the Glioma Recurrence in Post-radio/Chemotherapy Mixtures for Precise Pathology via Enzyme-Triggered Fluorescent Probe

机译:增强型γ-谷氨酰转肽酶成像,可通过酶触发的荧光探针揭示放射/化学治疗混合物中胶质瘤复发的精确病理情况

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摘要

Accurate pathological diagnosis of gliomas recurrence is crucial for the optimal management and prognosis prediction. The study here unravels that our newly developed γ-glutamyltranspeptidase (GGT) fluorescence probe () imaging in twenty recurrent glioma tissues selectively recognizes the most malignant portion from treatment responsive tissues induced by radio/chemo-therapy (). The overexpression of GGT in recurrent gliomas and low level in radiation necrosis were validated by western blot analysis and immunohistochemistry. Furthermore, the ki-67 index evaluation demonstrated the significant increase of malignancy, aided by the GGT-responsive fluorescent probe to screen out the right specimen through fast enhanced imaging of enzyme activity. Importantly, our GGT-targeting probe can be used for accurate determination of pathologic evaluation of tumor malignancy, and eventually for guiding the following management in patients with recurrent gliomas.(A) Schematic illustrations of GGT-catalyzed transformation of CN-BOD-GSH to CN-BOD-N and (B) the cartoon graph showed the process of the visualization of recurrent glioma for precise pathology diagnosis.
机译:胶质瘤复发的准确病理诊断对于最佳治疗和预后预测至关重要。这项研究揭开了我们新开发的在20个复发性神经胶质瘤组织中成像的γ-谷氨酰转肽酶(GGT)荧光探针()选择性地识别出放射/化学疗法诱导的治疗反应性组织中最恶性的部分。通过免疫印迹和免疫组织化学证实了复发性神经胶质瘤中GGT的过度表达和放射坏死的低水平。此外,ki-67指数评估证明了恶性肿瘤的显着增加,而GGT反应性荧光探针可通过快速增强的酶活性成像筛选出正确的标本。重要的是,我们的GGT靶向探针可用于准确确定肿瘤恶性的病理评估,并最终指导复发性神经胶质瘤患者的后续治疗。<!-fig ft0-> <!-fig mode = article f1-> <!-标题a7-> (A)的示意图说明了GGT催化的CN-BOD-GSH向CN-BOD-N和的转化(B)卡通图显示了复发性神经胶质瘤的可视化过程,以进行精确的病理诊断。

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