Article Summary
车莉萍1 程超2 张桉瑜2 冯菲2 崔斌2 孙高峰2 张建2 左长京2△.循环血游离Shope病毒DNA含量与兔VX2 肿瘤18F-FDG PET/CT 影像 表现的相关性分析*[J].现代生物医学进展英文版,2014,14(15):2808-2811.
循环血游离Shope病毒DNA含量与兔VX2 肿瘤18F-FDG PET/CT 影像 表现的相关性分析*
The Correlation between Cell-Free Shope Virus DNA Circulating in Plasmaand 18F-FDG PET/CT Imaging in VX2 Tumor-Bearing Rabbits*
  
DOI:
中文关键词: VX2 肿瘤  循环血游离DNA  氟[18F]-脱氧葡萄糖  正电子发射计算机断层  标准摄取值
英文关键词: VX2 tumor  ccfDNA (circulating cell free DNA)  18F-FDG  PET(Positron Emission Tomography)  SUV(Standard Uptake Value)
基金项目::上海市卫计委“新百人计划”基金(XBR2011040);上海市博士后科学基金(11R21410600);上海市人才发展资金(2010020); 长海医院“1255”学科建设基金(CH125521103)
Author NameAffiliation
CHE Li-ping, CHENG Chao, ZHANG An-yu,FENG Fei, CUI Bin, SUN Gao-feng, ZHANG Jian, ZUO Chang-jing 上海交通大学附属新华医院肿瘤科上海2000252 第二军医大学附属上海长海医院核医学科上海200020 
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中文摘要:
      摘要目的:探讨循环血中Shope 病毒DNA含量与兔VX2 肿瘤18F-FDG PET/CT 影像学特征间的关系及其临床意义。方法:采用 组织块接种法建立兔VX2肿瘤模型,并行18F-FDG PET-CT 观测肿瘤大小及糖代谢相关值,实时定量荧光探针PCR 法检测肿瘤 组织及血浆中Shope 病毒特征性DNA 片段含量。结果:移植前外周血中未检测出Shope 病毒特异性DNA片段;移植后2周, VX2 肿瘤组织和循环血中均可以检测到特征性Shope 病毒DNA 片段。瘤体内DNA 含量明显高于循环血中含量。循环血Shope 病毒DNA 含量与FDG-PET 的最大标准摄取值(SUVmax)明显呈正相关(r=0.943,p=0.005),但与肿瘤体积相关性尚不明确(r= 0.657,p=0.156)。结论:循环血Shope 病毒DNA有望作为一种潜在的VX2 肿瘤标志物,其廉价、无创的特性,有望在肿瘤的早期 诊断和预后随访中发挥优势。
英文摘要:
      ABSTRACT Objective:To investigate the relationship between 18F-FDG PET/CT imaging characteristics and circulating cell-free shope virus DNA copies, and to explore its clinical values. Methods:The VX2 tumor models in rabbit were established by transplanting VX2 tumor mass into leg muscles, and the shope virus DNA in tumor tissues and plasma was quantified by a quantitative real-time quantitative polymerase chain reaction (PCR) method.Results: Before tumor transplantation, no viral DNA was detected in peripheral blood; 14 days after transplantation circulating shope virus specific DNA fragments could be detected. Concentration of shope virus DNA in tumor tissue (mean (4.9± 1.9)× 106 copies/L) was significantly higher than that in the plasma (mean (1.3± 0.9)× 103 copies/L). There is a positive association between circulating shope DNA level and 18F-FDG-PET/CT maximum standard uptake value, but no significant association was observed between plasma shope virus DNA level and VX2 tumor size. Conclusion:Cell-free shope viral DNA in circulating plasma may be a tumor-marker of VX2 tumor animal model for cancer research, and circulating cell free tumor specific DNA may be proposed as a novel and early detectable bio-marker as well as an inexpensive and noninvasive assay for cancer management.
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