~(99)Tc~m-MIBI摄取与肿瘤辐照后细胞死亡或增殖活性的关系

Shuliang Lu, Jun Xiang, C. Qing, Shu-wen Jin, Z. Liao
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Differential uptake ratio (DUR) and tumor-to- nontarget (T/NT) ratio were used to quantitate the MIBI uptake. ②Single-cell suspension of tumor was prepared and apoptosis index (AI) was measured by flow cytometry; meanwhile, paraffin sections were stained with HE or proliferating cell nuclear antigen (PCNA) immunohistochemistrily, then percentages of necrosis area (PNA) and PCNA integral absorbance (PCNA-IA) were measured with a HPIAS-1000 imaging analysis system. Results ①Compared with the group with 0 Gy, the DUR of the groups with 10, 15, 20 Gy decreased markedly starting from 24 h post-irradiation and the decrease of DUR in 5 Gy group was much milder. Within the groups with similar irradiation dose, DUR kept decreasing with the time past irradiation. At the same post-irradiation time point, DUR decreased with dose escalating. The change of T/NT was similar to DUR. 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引用次数: 0

摘要

目的探讨99tc m-MIBI成像在肿瘤辐照后细胞活力监测中的应用价值。方法选取左大腿埃利希癌雌性昆明小鼠105只,分别以0、5、10、15、20 Gy单次剂量60 Co照射,分别于照射前6 h和照射后24、72、144 h(每组照射剂量或观察时间不同,每组6 ~ 8只):①采用99 Tc m-MIBI平面显像,切除肿瘤标本,用γ计数器计数放射性。采用差异摄取比(DUR)和肿瘤与非靶标比(T/NT)来量化MIBI的摄取。②制备肿瘤单细胞悬液,流式细胞术检测肿瘤细胞凋亡指数(AI);同时对石蜡切片进行HE或增殖细胞核抗原(PCNA)免疫组化染色,并用HPIAS-1000成像分析系统测定坏死面积百分比(PNA)和PCNA积分吸光度(PCNA- ia)。结果①与0 Gy组相比,10、15、20 Gy组的DUR从照射后24 h开始明显下降,5 Gy组DUR下降较轻。在辐照剂量相近的组内,随着辐照时间的延长,DUR持续降低。在同一照射后时间点,DUR随剂量增加而降低。T/NT变化与DUR相似。DUR与T/NT呈极好的线性相关(n=105, r=0.976, p0.01)。②与0 Gy组比较,辐照后24 h,各剂量组的AI和PNA均随剂量增加而升高,而PNA - ia则随剂量增加而降低。然而,在辐照后72和144 h, AI逆转至与0 Gy组相同的水平,PCNA-IA上升至接近0 Gy组的水平,但PNA持续升高。在同一时间点,PNA随剂量增加而增加。③辐照后24 h, DUR或T/NT与AI或PNA呈负相关(n=33, r =-0.849, -0.829;-0.883, -0.855, P < 0.01),与PCNA-IA呈正相关(n=33, r= 0.789, 0.742, P < 0.01)。在照射后72和144 h, DUR或T/NT仅与PNA呈负相关(n=33, r= -0.967, -0.956;-0.915, -0.886, P < 0.01)。结论99 Tc m-MIBI对肿瘤细胞的摄取与辐照后细胞活力的变化有关。Tc - m-MIBI成像可能有助于监测肿瘤细胞活力或照射后的治疗反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relationship between ~(99)Tc~m-MIBI uptake and cell death or proliferative activity after irradiation of tumor
Objective To evaluate the potential of 99 Tc m-MIBI imaging for monitoring cellular viability of tumor post-irradiation. Methods One hundred and five female Kunming mice bearing Ehrlich carcinoma in the left thigh were exposed to 60 Co at a single dose of 0, 5, 10, 15 and 20 Gy, respectively, and then the following protocols were performed at 6 h pre-irradiation and 24, 72, 144 h post-irradiation, respectively (every group with different irradiation dose or observation time consisted of six to eight mice): ① 99 Tc m-MIBI planer scintigraphy was performed, then the tumor sample was excised and its radioactivity was counted in a γ counter. Differential uptake ratio (DUR) and tumor-to- nontarget (T/NT) ratio were used to quantitate the MIBI uptake. ②Single-cell suspension of tumor was prepared and apoptosis index (AI) was measured by flow cytometry; meanwhile, paraffin sections were stained with HE or proliferating cell nuclear antigen (PCNA) immunohistochemistrily, then percentages of necrosis area (PNA) and PCNA integral absorbance (PCNA-IA) were measured with a HPIAS-1000 imaging analysis system. Results ①Compared with the group with 0 Gy, the DUR of the groups with 10, 15, 20 Gy decreased markedly starting from 24 h post-irradiation and the decrease of DUR in 5 Gy group was much milder. Within the groups with similar irradiation dose, DUR kept decreasing with the time past irradiation. At the same post-irradiation time point, DUR decreased with dose escalating. The change of T/NT was similar to DUR. There was a perfect linear correlation between DUR and T/NT ( n=105, r=0.976, P 0.01). ②Compared with the group with 0 Gy, at 24 h post-irradiation, the AI and PNA in other groups increased but PCNA-IA decreased with dose escalating. However, at 72 and 144 h post-irradiation, AI reversed to the same level as in 0 Gy group and PCNA-IA rose close to the level of 0 Gy group, but PNA increased continuously. At the same time point, PNA increased with dose escalating. ③At 24 h post-irradiation, DUR or T/NT was negatively correlated with AI or PNA ( n=33, r =-0.849, -0.829; -0.883, -0.855, respectively, P 0.01) and positively correlated with PCNA-IA ( n=33, r= 0.789, 0.742, respectively, P 0.01). At 72 and 144 h post-irradiation, DUR or T/NT was only negatively correlated with PNA ( n=33, r= -0.967, -0.956; -0.915, -0.886, respectively, P 0.01). Conclusions 99 Tc m-MIBI uptake of tumor cells correlated with the changes of cell viability after irradiation. 99 Tc m-MIBI imaging may be helpful to monitoring tumor cell viability or therapeutic response after irradiation.
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