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首页> 外文期刊>Translational Oncology >Rapid Cancer Fluorescence Imaging Using A γ-Glutamyltranspeptidase-Specific Probe For Primary Lung Cancer
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Rapid Cancer Fluorescence Imaging Using A γ-Glutamyltranspeptidase-Specific Probe For Primary Lung Cancer

机译:使用γ-谷氨酰转肽酶特异性探针对原发性肺癌进行快速癌症荧光成像

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BACKGROUND : We set out to examine the activity of γ-glutamyltranspeptidase (GGT) in lung cancer and the validity of γ-glutamyl hydroxymethyl rhodamine green (gGlu-HMRG) for intraoperative imaging of primary lung cancer. METHODS : GGT activities and mRNA expression levels of GGT1 (one of the GGT subtypes) in five human lung cancer cell lines were examined by fluorescence imaging and quantitative reverse transcription polymerase chain reaction. In vivo imaging of an orthotopic A549 xenograft model in nude mice was performed to confirm its applicability to intraoperative imaging. Furthermore, ex vivo imaging of 73 specimens from lung cancer patients were performed and analyzed to calculate the sensitivity/specificity of gGlu-HMRG for lung cancer diagnosis. RESULTS : GGT activities and mRNA expression levels of GGT1 are diverse depending on cell type; A549, H441, and H460 showed relatively high GGT activities and expression levels, whereas H82 and H226 showed lower values. In the in vivo mouse model study, tiny pleural dissemination and hilar/mediastinal lymph node metastasis (less than 1 mm in diameter) were clearly detected 15 minutes after topical application of gGlu-HMRG. In the ex vivo study of specimens from patients, the sensitivity and specificity of gGlu-HMRG were calculated to be 43.8% (32/73) and 84.9% (62/73), respectively. When limited to female patients, never smokers, and adenocarcinomas, these values were 78.9% (15/19) and 73.7% (14/19), respectively. CONCLUSIONS : Although GGT activity of lung cancer cells vary, gGlu-HMRG can serve as an intraoperative imaging tool to detect small foci of lung cancer when such cells have sufficient GGT activity.
机译:背景:我们着手研究γ-谷氨酰转肽酶(GGT)在肺癌中的活性以及γ-谷氨酰羟甲基罗丹明绿(gGlu-HMRG)在原发性肺癌术中成像中的有效性。方法:通过荧光成像和定量逆转录聚合酶链反应检测五种人类肺癌细胞系中GGT1活性(GGT亚型之一)的GGT活性和mRNA表达水平。在裸鼠体内进行原位A549异种移植模型的体内成像,以确认其在术中成像中的适用性。此外,对来自肺癌患者的73个标本进行了离体成像并进行了分析,以计算gGlu-HMRG对肺癌诊断的敏感性/特异性。结果:GGT1的GGT活性和mRNA表达水平因细胞类型而异。 A549,H441和H460显示相对较高的GGT活性和表达水平,而H82和H226显示较低的值。在体内小鼠模型研究中,局部应用gGlu-HMRG后15分钟即可清楚地检测到微小的胸膜播散和肺门/纵隔淋巴结转移(直径小于1毫米)。在离体患者标本的体外研究中,计算得出的gGlu-HMRG的敏感性和特异性分别为43.8%(32/73)和84.9%(62/73)。仅限于女性患者,从不吸烟者和腺癌,这些值分别为78.9%(15/19)和73.7%(14/19)。结论:尽管肺癌细胞的GGT活性有所不同,但当gGlu-HMRG具有足够的GGT活性时,它可以作为术中成像工具来检测肺癌的小灶。

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