Lafreniere R, Rosenberg S A
J Natl Cancer Inst. 1986 Feb;76(2):309-22.
A reproducible model for the selective generation of liver metastases has been developed. The spleen is exteriorized by means of a small subcostal incision and is directly injected with a 1-ml suspension of tumor cells. Tumor cells flow out of the splenic vein into the portal vein and lodge in the liver. Splenectomy is performed approximately 1 minute after tumor cell injection. The procedure is simple, requires a single operative procedure, and is applicable to a wide variety of tumors. Over a 6-month period, more than 3,000 such procedures with the use of 5 different tumors were performed in C57BL/6 mice, resulting in a 1.9% mortality. For reliable enumeration of the number of hepatic metastatic deposits, a suspension of india ink was injected iv, and the liver was removed and bleached with Fekete's solution. Tumor nodules appeared as discrete white nodules against the black background of normal liver parenchyma. This model provides a useful tool for the study of the experimental therapy of hepatic metastases in mice.
已经开发出一种用于选择性产生肝转移的可重复模型。通过一个小的肋下切口将脾脏外置,并直接注射1毫升肿瘤细胞悬液。肿瘤细胞从脾静脉流入门静脉并滞留在肝脏中。在注射肿瘤细胞后约1分钟进行脾切除术。该手术简单,只需一次手术操作,并且适用于多种肿瘤。在6个月的时间里,在C57BL/6小鼠中使用5种不同的肿瘤进行了3000多次这样的手术,死亡率为1.9%。为了可靠地计数肝转移灶的数量,静脉注射印度墨汁悬液,然后取出肝脏并用费克特溶液漂白。肿瘤结节在正常肝实质的黑色背景下呈现为离散的白色结节。该模型为研究小鼠肝转移的实验性治疗提供了一个有用的工具。