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作 者:李亚军[1] 白人驹[1] 高硕[2] 李彦生[2] 刘磊[2] 贾薇[2] 蔡莉[2] 邢喜玲[2]
机构地区:[1]天津医科大学总医院放射科,300052 [2]天津医科大学总医院PET-CT中心,300052
出 处:《国际放射医学核医学杂志》2010年第3期139-142,共4页International Journal of Radiation Medicine and Nuclear Medicine
摘 要:目的探讨^11C-胆碱和^18F-FDGPET—CT反映兔VX2肺肿瘤血管生成的效能。方法新西兰大白兔54只,右肺接种VX2肿瘤10—11d后,行^11C-胆碱和^18F-FDGPET—CT,测量肿瘤^11C-胆碱和^18F—FDG最大标准化摄取值(SUVmax)。同时,测量肿瘤标本大小,用免疫组化方法评价肿瘤微血管密度(MVD)。然后对肿瘤胆碱SUVmax。^18F、FDG SUVmax与肿瘤大小、MVD进行相关性分析。结果33只实验兔成功完成所有检查,得到VX2肺肿瘤的^11C-胆碱SUVmax平均值为4.02±3.07(1.4~12.2),对^18F—FDG的SUVmax平均值为5.70±3.45(1.0—13.0),肿瘤大小平均值为(1.68±1.61)cm^3(0.13—8.00cm^3)。高倍镜(200倍,0.739mm^2)视野下,肿瘤MVD平均值为(35.8±13.6)个(13—64个)。经统计学分析,^11C-胆碱SUVmax与肿瘤大小及MVD之间均不具有相关性;^18F-FDG SUVmax与MVD(r=0.525,P=0.002)之间存在正相关关系,与肿瘤大小(r=0.335,P=-0.057)之间呈临界正相关关系。结论^18F—FDG PET-CT可反映兔VX2肺肿瘤血管生成,^11C-胆碱PET-CT不能反映肿瘤血管生成。Objective To evaluate and compare the suitability of ^11C-choline and ^18F-FDG PET-CT for refleeting tumors angiogenesis. Methods Fifty-four New Zealand white rabbits whieh weighted 2.5-3.0 kg were used in the experiment. Under general anesthesia, a needle was transthoraeically inserted into the right lung, 0.5 ml viable VX2 tumor cell suspension was slowly injected through the needle to establish the model. ^11C-ehaline and ^18F-FDG PET-CT were performed after 10-11 d. The tumors SUVmax, were calculated. The sections were stained with hematoxylin and eosin, and immunostained for CD34. Assessment of mierovessel density(MVD) was performed by computer-assisted image analysis. The relationship ^11C-eholine SUVmax and ^18F-FDG SUVmax with tumor size and MVD were statistically analyzed. Results Thirty-three rabbits successfully completed all imaging examinations, ^11C-choline and ^18F-FDG differently accumulated in all lung VX2 tumors. The mean of HC-eholine SUVmax was 4.02+3.07 (1.4-12.2), and the mean of ^18F-FDG SUVmax was 5.70+3.45 (1.0-13.0). The mean size of tumor was (1.68+1.61)cm^3 (0.13-8.00 cm^3). Under high power microscope field of vision (200x, 0.739 mm^2), the mean of MVD was 35.8+13.6 (13-64). ^11C-eholine SUVmax, did not correlate with tumor size and MVD. ^18F-FDG SUVmax significantly and positively related to MVD (r= 0.525, P=0.002). There was a eritieal positive correlation between ^18F-FDG SUVmax and tumor size (r=0.335, P=0.057). Conclusions In the rabbit VX2 lung tumor model, ^18F-FDG SUVmax correlated with MVD, so ^18F- FDG PET-CT could reflect tumor angiogenesis. ^11C-eholine SUVmax did not statistically correlate with MVD, and ^11C-choline PET-CT could not reflect tumor angiogenesis.
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