Osaku M, Ueda M, Ando N, Shinozawa Y, Hirota N, Shimizu N, Abe O
Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
Anticancer Res. 1991 Nov-Dec;11(6):1951-6.
We determined in vitro the antitumor activity of a conjugate prepared by binding a monoclonal antibody (B4G7), which recognizes the human epidermal growth factor (EGF) receptor, with peplomycin (PEP), which is an antitumor agent effective against squamous cell carcinoma. This B4G7-PEP conjugate was prepared by coupling of B4G7 and carboxymethylpeplomycin active ester. The conjugate killed A431 cells of squamous cell carcinoma which overexpress EGF receptors at lower concentrations than PEP alone. On the basis of its IC50, the conjugate was six times more potent than PEP alone. A simple mixture of B4G7 and PEP was as effective as PEP alone in cytotoxicity. The addition of ten times the amounts of B4G7 to this conjugate decreased its cytotoxicity. When other squamous cell carcinoma cell lines with different levels of EGF receptors (NA, Ca9-22, TE-1, TE-8) were treated with the conjugate, cells were killed dose-dependently and the cytotoxicity was dependent on the number of EGF receptors. When each squamous cell carcinoma cell line was treated with a control conjugate prepared by combining PEP with mouse IgG instead of B4G7, no cytotoxicity was observed. These results indicate that B4G7-PEP will be a useful weapon in multidisciplinary treatment which utilizes the EGF receptor, as these receptors are detected in a higher incidence in squamous cell carcinoma.
我们在体外测定了一种偶联物的抗肿瘤活性,该偶联物是通过将识别人类表皮生长因子(EGF)受体的单克隆抗体(B4G7)与平阳霉素(PEP,一种对鳞状细胞癌有效的抗肿瘤药物)结合制备而成。这种B4G7-PEP偶联物是通过B4G7与羧甲基平阳霉素活性酯偶联制备的。该偶联物在比单独使用PEP更低的浓度下就能杀死过表达EGF受体的鳞状细胞癌A431细胞。基于其半数抑制浓度(IC50),该偶联物的效力是单独使用PEP的六倍。B4G7和PEP的简单混合物在细胞毒性方面与单独使用PEP的效果相同。向该偶联物中加入十倍量的B4G7会降低其细胞毒性。当用该偶联物处理其他具有不同EGF受体水平的鳞状细胞癌细胞系(NA、Ca9-22、TE-1、TE-8)时,细胞呈剂量依赖性死亡,且细胞毒性取决于EGF受体的数量。当用通过将PEP与小鼠IgG而非B4G7结合制备的对照偶联物处理每个鳞状细胞癌细胞系时,未观察到细胞毒性。这些结果表明,B4G7-PEP将成为利用EGF受体的多学科治疗中的一种有用武器,因为这些受体在鳞状细胞癌中的检出率较高。