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新型临床前胰腺癌研究模型的建立:生物发光成像引导的局部照射和原位移植瘤的肿瘤监测。

Development of a novel preclinical pancreatic cancer research model: bioluminescence image-guided focal irradiation and tumor monitoring of orthotopic xenografts.

机构信息

Department of Radiation Oncology & Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Transl Oncol. 2012 Apr;5(2):77-84. doi: 10.1593/tlo.11316. Epub 2012 Apr 1.

Abstract

PURPOSE

We report on a novel preclinical pancreatic cancer research model that uses bioluminescence imaging (BLI)-guided irradiation of orthotopic xenograft tumors, sparing of surrounding normal tissues, and quantitative, noninvasive longitudinal assessment of treatment response.

MATERIALS AND METHODS

Luciferase-expressing MiaPaCa-2 pancreatic carcinoma cells were orthotopically injected in nude mice. BLI was compared to pathologic tumor volume, and photon emission was assessed over time. BLI was correlated to positron emission tomography (PET)/computed tomography (CT) to estimate tumor dimensions. BLI and cone-beam CT (CBCT) were used to compare tumor centroid location and estimate setup error. BLI and CBCT fusion was performed to guide irradiation of tumors using the small animal radiation research platform (SARRP). DNA damage was assessed by γ-H2Ax staining. BLI was used to longitudinally monitor treatment response.

RESULTS

Bioluminescence predicted tumor volume (R = 0.8984) and increased linearly as a function of time up to a 10-fold increase in tumor burden. BLI correlated with PET/CT and necropsy specimen in size (P < .05). Two-dimensional BLI centroid accuracy was 3.5 mm relative to CBCT. BLI-guided irradiated pancreatic tumors stained positively for γ-H2Ax, whereas surrounding normal tissues were spared. Longitudinal assessment of irradiated tumors with BLI revealed significant tumor growth delay of 20 days relative to controls.

CONCLUSIONS

We have successfully applied the SARRP to a bioluminescent, orthotopic preclinical pancreas cancer model to noninvasively: 1) allow the identification of tumor burden before therapy, 2) facilitate image-guided focal radiation therapy, and 3) allow normalization of tumor burden and longitudinal assessment of treatment response.

摘要

目的

我们报告了一种新的胰腺癌临床前研究模型,该模型使用生物发光成像(BLI)引导的肿瘤原位移植照射,避免了周围正常组织受到照射,并对治疗反应进行定量、非侵入性的纵向评估。

材料和方法

将表达荧光素酶的 MiaPaCa-2 胰腺癌细胞原位注射到裸鼠体内。将 BLI 与病理肿瘤体积进行比较,并随时间评估光子发射。BLI 与正电子发射断层扫描(PET)/计算机断层扫描(CT)相关联,以估计肿瘤尺寸。BLI 和锥形束 CT(CBCT)用于比较肿瘤中心点位置并估计设置误差。BLI 和 CBCT 融合用于使用小动物辐射研究平台(SARRP)引导肿瘤照射。通过γ-H2Ax 染色评估 DNA 损伤。BLI 用于纵向监测治疗反应。

结果

生物发光预测肿瘤体积(R = 0.8984),并随时间呈线性增加,直到肿瘤负荷增加 10 倍。BLI 与 PET/CT 和尸检标本的大小相关(P <.05)。二维 BLI 中心点的准确性相对于 CBCT 为 3.5 毫米。BLI 引导的胰腺肿瘤照射后γ-H2Ax 染色阳性,而周围正常组织则免受照射。BLI 对照射肿瘤的纵向评估显示,与对照组相比,肿瘤生长延迟了 20 天。

结论

我们成功地将 SARRP 应用于生物发光的原位临床前胰腺癌模型,以非侵入性地:1)在治疗前识别肿瘤负担,2)促进图像引导的焦点放射治疗,3)使肿瘤负担正常化并对治疗反应进行纵向评估。

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