Koda K, Nakajima N, Saito N, Yasutomi J, McKnight M E, Glassy M C
Department of Surgery I, Chiba University School of Medicine, Chiba City, Japan.
Br J Cancer. 1998 Nov;78(10):1313-22. doi: 10.1038/bjc.1998.677.
We characterized a natural human antibody to adenocarcinomas and investigated the biological role of this Ab/Ag complex in cancer expansion. Human monoclonal antibodies (HuMAbs) were generated with hybridoma fusion methods using regional nodal lymphocytes of colon carcinoma patients. Among 1036 HuMAbs, only one, termed SK1, an IgM, was adenocarcinoma specific in the immunohistochemical study. The antigen recognized by SK1 (Ag-SK1) was a glycoprotein with a molecular weight of 42-46 kDa. The expression of Ag-SK1 on carcinoma cells varied according to the cell growth periods but was independent of cell cycle state as elucidated by two-colour fluorescence-activated cell sorter (FACS) analysis. A dot-blot analysis showed that the concentration of Ag-SK1 per total protein differed considerably among eight colon carcinoma cells examined and that the difference was closely correlated with the invasion capacity of the cells as assessed by a microchemotaxis assay. Furthermore, up to 87% of cell migration was inhibited by SK1 in a dose-dependent manner. These data suggested that Ag-SK1 is metabolized and expressed on highly invasive carcinoma cells. In addition, it appears that, although rare, some patients do mount an anti-cancer antigen response in their draining lymph nodes. A HuMAb such as SK1 may be a good candidate for the treatment of cancer invasion and metastasis.
我们对一种针对腺癌的天然人类抗体进行了特性分析,并研究了这种抗体/抗原复合物在癌症扩散中的生物学作用。利用结肠癌患者的区域淋巴结淋巴细胞,通过杂交瘤融合方法产生了人类单克隆抗体(HuMAbs)。在1036种HuMAbs中,在免疫组织化学研究中,只有一种名为SK1的IgM对腺癌具有特异性。SK1识别的抗原(Ag-SK1)是一种分子量为42 - 46 kDa的糖蛋白。通过双色荧光激活细胞分选仪(FACS)分析表明,Ag-SK1在癌细胞上的表达随细胞生长时期而变化,但与细胞周期状态无关。斑点印迹分析显示,在所检测的8种结肠癌细胞中,Ag-SK1占总蛋白的浓度差异很大,且这种差异与通过微趋化分析评估的细胞侵袭能力密切相关。此外,SK1以剂量依赖的方式抑制高达87%的细胞迁移。这些数据表明,Ag-SK1在高侵袭性癌细胞上被代谢并表达。此外,似乎尽管罕见,但一些患者在其引流淋巴结中确实会产生抗癌抗原反应。像SK1这样的HuMAb可能是治疗癌症侵袭和转移的良好候选药物。