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阿霉素-单克隆抗体偶联物对人膀胱癌的抗肿瘤活性

Antitumor activity of doxorubicin-monoclonal antibody conjugate on human bladder cancer.

作者信息

Yu D S, Chu T M, Yeh M Y, Chang S Y, Ma C P, Han S H

机构信息

Department of Diagnostic Immunology Research and Biochemistry, Roswell Park Memorial Institute, Buffalo, NY 14263.

出版信息

J Urol. 1988 Aug;140(2):415-21. doi: 10.1016/s0022-5347(17)41648-x.

Abstract

Doxorubicin (adriamycin) was conjugated via the dextran bridge method to a murine IgG3 monoclonal antibody, 1G3.10, directed against human bladder cancer. The drug-antibody conjugate, prepared from using 25% oxidized dextran as the linker, retained essentially the original immunological activity of the antibody using ELISA as tested against an antigen-positive target cell line (TSGH-8301), which has been shown to express an antigen recognized by the monoclonal antibody 1G3.10. Antitumor effect of the conjugate in vitro was evaluated by its inhibition on 3H-uridine incorporation into the established human bladder cancer cells. The conjugate exhibited a significantly higher cytotoxicity on target TSGH-8301 cells than that by a control antibody-doxorubicin conjugate prepared identically from an irrelevant mouse IgG3 monoclonal antibody. No apparently different cytotoxicity was detected on control antigen-negative bladder tumor cells of J82 between these two drug-antibody conjugates. Verapamil, a calcium channel blocker, enhanced the in vitro cytotoxicity of doxorubicin-1G3.10 monoclonal antibody conjugate. Results obtained from in vivo evaluation using xenografted target TSGH-8301 bladder tumor indicated that the 1G3.10 monoclonal antibody conjugate containing doxorubicin injected 4X, i.p., significantly inhibited TSGH-8301 bladder tumor growth in nude mice, whereas free monoclonal antibody, free drug and the mixture of both showed only moderate inhibition of tumor growth as compared to the untreated control. Verapamil also enhanced in vivo antitumor activity of the conjugate. There was no side effect (weight loss) detected on the conjugate-treated mice. Results obtained from in vivo evaluation using xenografted control J82 bladder tumor showed no specific antitumor activity as exhibited by doxorubicin-1G3.10 monoclonal antibody conjugate in comparison with free drug, mixture of drug and antibody without conjugation, or doxorubicin conjugated to the irrelevant antibody. These results suggested that doxorubicin conjugated with bladder tumor associated monoclonal antibody could be useful as a potentially cytotoxic agent in immunochemotherapy of human bladder cancer.

摘要

多柔比星(阿霉素)通过葡聚糖桥接方法与一种针对人膀胱癌的鼠源IgG3单克隆抗体1G3.10偶联。使用25%氧化葡聚糖作为连接子制备的药物-抗体偶联物,通过酶联免疫吸附测定法(ELISA)检测,针对抗原阳性靶细胞系(TSGH-8301)测试时,保留了抗体基本的原始免疫活性,该细胞系已被证明表达可被单克隆抗体1G3.10识别的抗原。通过评估其对3H-尿苷掺入已建立的人膀胱癌细胞的抑制作用,来评价该偶联物在体外的抗肿瘤效果。与由不相关的鼠源IgG3单克隆抗体制备的对照抗体-多柔比星偶联物相比,该偶联物对靶TSGH-8301细胞表现出显著更高的细胞毒性。在这两种药物-抗体偶联物之间,未检测到对J82对照抗原阴性膀胱肿瘤细胞有明显不同的细胞毒性。钙通道阻滞剂维拉帕米增强了多柔比星-1G3.10单克隆抗体偶联物的体外细胞毒性。使用移植了靶TSGH-8301膀胱肿瘤的异种移植模型进行体内评估得到的结果表明,腹腔注射4次含多柔比星的1G3.10单克隆抗体偶联物,可显著抑制裸鼠体内TSGH-8301膀胱肿瘤的生长,而游离单克隆抗体、游离药物以及两者的混合物与未治疗的对照相比,仅表现出对肿瘤生长的中度抑制。维拉帕米也增强了该偶联物的体内抗肿瘤活性。在接受偶联物治疗的小鼠中未检测到副作用(体重减轻)。使用移植了对照J82膀胱肿瘤的异种移植模型进行体内评估得到的结果显示,与游离药物、未偶联的药物和抗体混合物或与不相关抗偶联的多柔比星相比,多柔比星-1G3.10单克隆抗体偶联物未表现出特异性抗肿瘤活性。这些结果表明,与膀胱肿瘤相关单克隆抗体偶联的多柔比星,可能作为一种潜在的细胞毒性药物用于人膀胱癌的免疫化学治疗。

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