Nikfarjam Mehrdad, Yeo Dannel, He Hong, Baldwin Graham, Fifis Theodora, Costa Patricia, Tan Bryan, Yang Eunice, Wen Shu wen, Christophi Christopher
1 Department of Surgery, Austin Health, University of Melbourne, Austin Health, LTB8, Heidleberg, Victoria, Australia.
J Invest Surg. 2013 Dec;26(6):352-9. doi: 10.3109/08941939.2013.797057. Epub 2013 Aug 19.
Pancreatic adenocarcinoma has an extremely poor prognosis. The use of appropriate in vivo models is essential in devising methods to improve treatment outcomes.
A pancreatic adenocarcinoma model based on tumor injection into the pancreatic head was compared with a pancreatic tail injection model in C57/BL6 mice. The murine pancreatic adenocarcinoma cell line PAN02, dispersed in Matrigel™, was used for tumor induction.
Tumors developed in all animals in both models. Tumor size was more consistent within the pancreatic tail group at 20 days following induction, with no evidence of metastatic disease. Animals in the pancreatic head injection group showed signs of reduced health by 20 days following injection and developed jaundice. Microscopic liver metastases were noted in some of these animals at this time point. The overall survival of animals at 40 days following tumor induction was significantly lower in the pancreatic head injection group (0% vs. 35%; p < .001). Multiple liver metastases were noted in five of 10 (50%) animals in the head injection group, without evidence of peritoneal metastases. In the pancreatic tail injection group, 18 of 20 (90%) animals had multiple peritoneal metastases, and nine of 20 (45%) animals had evidence of isolated liver deposits. Tumors in both regions of the pancreas had similar histologic characteristics, with a dense fibrotic stroma at the interface between the tumor and the normal pancreas.
Pancreatic head and tail orthotopic cancer models produce consistent tumors, but the patterns of tumor spread and survival differ according to the site of injection.
胰腺腺癌预后极差。使用合适的体内模型对于设计改善治疗结果的方法至关重要。
在C57/BL6小鼠中,将基于肿瘤注射到胰头的胰腺腺癌模型与胰尾注射模型进行比较。将分散在基质胶™中的小鼠胰腺腺癌细胞系PAN02用于诱导肿瘤。
两种模型中的所有动物均出现肿瘤。诱导后20天,胰尾组的肿瘤大小更一致,且无转移疾病迹象。胰头注射组的动物在注射后20天出现健康状况下降的迹象,并出现黄疸。此时在其中一些动物中发现了微观肝转移。肿瘤诱导后40天,胰头注射组动物的总体生存率显著较低(0%对35%;p<.001)。在头注射组的10只动物中有5只(50%)发现多处肝转移,无腹膜转移迹象。在胰尾注射组中,20只动物中有18只(90%)有多处腹膜转移,20只动物中有9只(45%)有孤立肝转移灶迹象。胰腺两个区域的肿瘤具有相似的组织学特征,在肿瘤与正常胰腺的界面处有致密的纤维化基质。
胰头和胰尾原位癌模型产生的肿瘤一致,但肿瘤扩散模式和生存率因注射部位而异。