Wang Bailiang, Shi Qian, Abbruzzese James, Xiong Qinghua, Le Xiangdong, Xie Keping
Department of Gastrointestinal Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030.
Int J Gastrointest Cancer. 2001;29(1):37-46.
In this study, we report a metastatic model of Panc02 murine pancreatic adenocarcinoma. Parental Panc02cells were orthotopically implanted into the pancreas of syngeneic C57BL/6 mice. Tumor cells were isolatedfrom liver micrometastases 90 d after tumor implantation and established as a culture (Panc02-H1).The Panc02-H1 cells were then implanted into the pancreas of mice. Liver metastases were then collectedand established as Panc02-H2 cells. This process was repeated until the Panc02-H7 cell line was established.These cells were extremely aggressive after implantation as manifested by progressive growth in the pancreas,peritoneal dissemination, and distant metastasis to multiple organs, including the liver and lungs.Moreover, Panc02-H7 cells expressed the inducible nitric oxide synthase gene at a very low level in cultureand produced highly vascularized tumors having a large number of infiltrating macrophages. Collectively,this model system should be a valuable tool for investigating the molecular mechanisms governing pancreaticcancer growth and metastasis and exploring potential treatment modalities for this disease.
在本研究中,我们报告了一种Panc02小鼠胰腺腺癌的转移模型。将亲代Panc02细胞原位植入同基因C57BL/6小鼠的胰腺。肿瘤植入90天后,从肝脏微转移灶中分离肿瘤细胞并建立培养物(Panc02-H1)。然后将Panc02-H1细胞植入小鼠胰腺。接着收集肝转移灶并建立为Panc02-H2细胞。重复此过程,直到建立Panc02-H7细胞系。这些细胞植入后极具侵袭性,表现为在胰腺中进行性生长、腹膜播散以及远处转移至包括肝脏和肺在内的多个器官。此外,Panc02-H7细胞在培养中诱导型一氧化氮合酶基因表达水平极低,并产生具有大量浸润巨噬细胞的高度血管化肿瘤。总体而言,该模型系统应是研究胰腺癌生长和转移的分子机制以及探索该疾病潜在治疗方式的有价值工具。