Fujihara T, Sawada T, Hirakawa K, Chung Y S, Yashiro M, Inoue T, Sowa M
First Department of Surgery, Osaka City University Medical School, Osaka, Japan.
Clin Exp Metastasis. 1998 May;16(4):389-98. doi: 10.1023/a:1006550704555.
The actual mechanisms responsible for lymph node metastasis in gastric cancer are still unclear. To investigate the mechanisms of lymph node metastasis in gastric cancer, we established a lymph node metastatic model for human scirrhous gastric carcinoma. Lymph node metastasis had frequently developed after orthotopic implantation of OCUM-2M LN derived from a scirrhous gastric cancer cell line, OCUM-2M, which had low capacity for lymph node metastasis. We elucidated the different characteristics including binding ability, migratory capacity and immunoresponses induced by the cell surface molecules of these two cell lines. The binding ability to Matrigel and migratory capacity of OCUM-2M LN cells were significantly greater than those of OCUM-2M cells. On flow cytometric analysis, both OCUM-2M and OCUM-2M LN cells strongly expressed HLA-I (99.5 and 97.1%) and LFA-3 (76.6 and 99.2%) in level of expression between the two cell lines, but neither cell line expressed HLA-II (0.0 and 0.0%), B7-1 (0.0 and 0.0%) or B7-2 (0.4 and 0.3%). ICAM-1 expression in OCUM-2M LN cells was weaker (0.7%) than that in OCUM-2M cells (36.8%). Strong adhesiveness and cytotoxicity of mononuclear lymphocytes for OCUM-2M cells were observed in adhesion and cytotoxic assays, both of which were significantly decreased by the addition of anti-ICAM-1 antibodies. On the other hand, the adhesiveness and cytotoxicity of OCUM-2M LN cells were significantly less than those of OCUM-2M cells, and were not affected by the addition of anti-ICAM-1 antibodies. These findings suggest that decreased ICAM-1 expression in a new gastric cancer cell line with a high rate of lymph node metastasis may in turn decrease immune responses mediated through LFA-1-dependent effector cell adhesion, and that this escape from the immunosurveillance system may be one of the factors inducing lymph node metastasis. In conclusion, we established a gastric cancer cell line, OCUM-2M LN, with a high rate of lymph node metastasis. An in vivo lymph node-metastatic model with this cell line should be useful for analysing the mechanism and therapeutic approach of lymph node metastasis.
胃癌淋巴结转移的实际机制仍不清楚。为了研究胃癌淋巴结转移的机制,我们建立了人硬癌性胃癌的淋巴结转移模型。原位植入源自低淋巴结转移能力的硬癌胃癌细胞系OCUM - 2M的OCUM - 2M LN后,淋巴结转移频繁发生。我们阐明了这两种细胞系的细胞表面分子诱导的不同特性,包括结合能力、迁移能力和免疫反应。OCUM - 2M LN细胞对基质胶的结合能力和迁移能力明显大于OCUM - 2M细胞。流式细胞术分析显示,OCUM - 2M和OCUM - 2M LN细胞均强烈表达HLA - I(分别为99.5%和97.1%)和LFA - 3(分别为76.6%和99.2%),两种细胞系之间表达水平相近,但两种细胞系均不表达HLA - II(均为0.0%)、B7 - 1(均为0.0%)或B7 - 2(分别为0.4%和0.3%)。OCUM - 2M LN细胞中ICAM - 1的表达(0.7%)比OCUM - 2M细胞中(36.8%)弱。在黏附试验和细胞毒性试验中观察到单核淋巴细胞对OCUM - 2M细胞有较强的黏附性和细胞毒性,添加抗ICAM - 1抗体后两者均显著降低。另一方面,OCUM - 2M LN细胞的黏附性和细胞毒性明显低于OCUM - 2M细胞,且不受抗ICAM - 1抗体添加的影响。这些发现表明,在具有高淋巴结转移率的新胃癌细胞系中ICAM - 1表达降低可能反过来降低通过LFA - 1依赖的效应细胞黏附介导的免疫反应,并且这种对免疫监视系统的逃避可能是诱导淋巴结转移的因素之一。总之,我们建立了一种具有高淋巴结转移率的胃癌细胞系OCUM - 2M LN。使用该细胞系建立的体内淋巴结转移模型应有助于分析淋巴结转移的机制和治疗方法。