Moats R, Ma L Q, Wajed R, Sugiura Y, Lazaryev A, Tyszka M, Jacobs R, Fraser S, Nelson M D, DeClerck Y A
Childrens Hospital Los Angeles, Department of Pediatrics, USC Keck School of Medicine, California 90027, USA.
Clin Exp Metastasis. 2000;18(6):455-61. doi: 10.1023/a:1011827122126.
Neuroblastoma is the second most common solid tumor in children. So far few tumor models for this cancer have been reported in mice. We have created a murine tumor model for studying human neuroblastoma based on surgical orthotopic implantation in scid mice. Small fragments of subcutaneous tumors of SK-N-BE(2) human neuroblastoma cells expressing enhanced green fluorescent protein were surgically implanted near the left adrenal gland of scid mice. One hundred percent of the animals (n = 21) successfully implanted developed a large retroperitoneal tumor and became moribund between 22 and 57 days after implantation (mean survival time = 41 days). At the time of sacrifice the presence of bone marrow metastasis was detected by RT-PCR for green fluorescent protein in 95% of the cases. The growth of small tumor implants could be easily visualized and quantified by surveillance MR imaging, with a resolution of 117 x 117 x 750 microm in two orthogonal planes allowing accurate volume measurements, as well as assessment of necrosis and tissue invasion. This novel model should be a valuable tool to study the biology and therapeutic approaches to neuroblastoma.
神经母细胞瘤是儿童中第二常见的实体瘤。到目前为止,在小鼠中报道的这种癌症的肿瘤模型很少。我们基于在严重联合免疫缺陷(scid)小鼠中的手术原位植入,创建了一种用于研究人类神经母细胞瘤的小鼠肿瘤模型。将表达增强型绿色荧光蛋白的SK-N-BE(2)人神经母细胞瘤细胞的皮下肿瘤小片段手术植入scid小鼠的左肾上腺附近。100%成功植入的动物(n = 21)在植入后22至57天之间出现了巨大的腹膜后肿瘤并濒死(平均生存时间 = 41天)。在处死时,通过逆转录聚合酶链反应(RT-PCR)检测绿色荧光蛋白,在95%的病例中检测到骨髓转移。小肿瘤植入物的生长可以通过监测磁共振成像轻松可视化和量化,在两个正交平面上的分辨率为117×117×750微米,允许进行准确的体积测量以及坏死和组织侵袭的评估。这种新模型应该是研究神经母细胞瘤生物学和治疗方法的有价值工具。