Sakata K, Kozaki K, Iida K, Tanaka R, Yamagata S, Utsumi K R, Saga S, Shimizu S, Matsuyama M
Department of Pathology, Nagoya University School of Medicine.
Jpn J Cancer Res. 1996 Jan;87(1):78-85. doi: 10.1111/j.1349-7006.1996.tb00203.x.
We established and characterized high- (LuM1) and low-lung-metastatic (NM11) cell lines derived from murine colon adenocarcinoma 26 tumor line. LuM1 cell line was established as a clonal cell line from a cultured cell mixture derived from a lung-metastatic nodule after 7 sequential subcutaneous transplantations of lung-metastatic tumors in the abdominal wall of BALB/c mice. NM11 cell line was established from a cultured cell mixture derived from a subcutaneous transplant of murine colon adenocarcinoma 26 tumor cells. LuM1 cells showed marked spontaneous lung metastases, but NM11 cells rarely did. High invasive potential of LuM1 cells was revealed by in vitro invasion assay using Matrigel reconstituted membranes. Rapid retraction was observed in monolayers of human umbilical vein endothelial cells and bovine aortic endothelial cells when LuM1 cells were added on the monolayers. Gelatin zymography and immunochemical examinations with monoclonal antibodies against gelatinase B (Mr 95,000 type IV collagenase) showed secretion of large amounts of the gelatinase by LuM1 cells.
我们建立并鉴定了源自小鼠结肠腺癌26肿瘤系的高肺转移(LuM1)和低肺转移(NM11)细胞系。LuM1细胞系是通过将肺转移瘤在BALB/c小鼠腹壁进行7次连续皮下移植后,从源自肺转移结节的培养细胞混合物中建立的克隆细胞系。NM11细胞系是从源自小鼠结肠腺癌26肿瘤细胞皮下移植的培养细胞混合物中建立的。LuM1细胞表现出明显的自发性肺转移,而NM11细胞很少发生肺转移。使用基质胶重组膜进行的体外侵袭试验显示LuM1细胞具有高侵袭潜力。当在人脐静脉内皮细胞和牛主动脉内皮细胞单层上添加LuM1细胞时,观察到单层细胞迅速回缩。明胶酶谱分析以及使用抗明胶酶B(分子量95,000的IV型胶原酶)单克隆抗体进行的免疫化学检查显示,LuM1细胞分泌大量的明胶酶。