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去甲光环肽与抗表皮生长因子受体单克隆抗体的免疫毒素偶联物对表皮生长因子受体高表达肿瘤的抑制作用

Suppression of an epidermal growth factor receptor-hyperproducing tumor by an immunotoxin conjugate of gelonin and a monoclonal anti-epidermal growth factor receptor antibody.

作者信息

Hirota N, Ueda M, Ozawa S, Abe O, Shimizu N

机构信息

Research and Development Division, Iwasaki Electric Co., Ltd., Saitama-Ken, Japan.

出版信息

Cancer Res. 1989 Dec 15;49(24 Pt 1):7106-9.

PMID:2555059
Abstract

An immunotoxin was made by conjugating a murine monoclonal antibody (B4G7) that recognizes the human epidermal growth factor (EGF) receptor with gelonin, a ribosome-inactivating protein. This B4G7-gelonin conjugate was shown to be specifically cytotoxic for EGF receptor-hyperproducing cells. The conjugate was tested in nude mice and shown to be capable of suppressing the growth of an EGF receptor-hyperproducing squamous carcinoma cell (A431) solid tumor. Nude mice bearing an A431 cell tumor that were given injections i.p. for 5 consecutive days with at least 10 micrograms of the conjugate showed significant suppression of tumor growth for about 7 days. On the other hand, an unconjugated mixture of B4G7 and gelonin showed no specific antitumor activity against the A431 cell tumor. The growth of an EGF receptor-deficient small cell lung cancer cell (H69) tumor was not suppressed by injection of the conjugate. No toxic effects were observed in histological examination of nontumorous tissues of mice treated with at least 250 micrograms of conjugate per mouse. These results suggest that the conjugate may be useful for targeting therapy to EGF receptor-hyperproducing squamous carcinoma.

摘要

通过将识别人类表皮生长因子(EGF)受体的鼠单克隆抗体(B4G7)与核糖体失活蛋白相思豆毒素交联,制备了一种免疫毒素。已证明这种B4G7 - 相思豆毒素缀合物对过度产生EGF受体的细胞具有特异性细胞毒性。该缀合物在裸鼠中进行了测试,结果表明它能够抑制过度产生EGF受体的鳞状癌细胞(A431)实体瘤的生长。携带A431细胞瘤的裸鼠腹腔注射至少10微克缀合物,连续注射5天,结果显示肿瘤生长在大约7天内受到显著抑制。另一方面,B4G7和相思豆毒素的未交联混合物对A431细胞瘤没有显示出特异性抗肿瘤活性。注射缀合物并未抑制缺乏EGF受体的小细胞肺癌细胞(H69)肿瘤的生长。对每只小鼠注射至少250微克缀合物处理后的小鼠非肿瘤组织进行组织学检查,未观察到毒性作用。这些结果表明,该缀合物可能对靶向治疗过度产生EGF受体的鳞状癌有用。

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