Sacchi A, Kennel S J, Apollonj C, Natali P G
Cancer Treat Rep. 1985 Sep;69(9):985-91.
The growth and dissemination of Lewis lung carcinoma have been analyzed following treatment of isolated tumor cells or of tumor-bearing animals with monoclonal antibody (MoAb) 135-13C, which recognizes a cell surface tumor-associated protein of 180,000 daltons. The results of this study indicate that MoAb 135-13C binds with high affinity to Lewis lung tumor cells and induces different effects on the primary tumor (20%-25% reduction of tumor weight) and its metastasis (twofold increase of lung nodule formation). Different schedules of MoAb 135-13C administration have shown that these effects are dose- and time-dependent. In particular, the maximum increase in metastasis formation is observed when the MoAb 135-13C is administered at time of systemic tumor dissemination. In vitro preincubation of tumor cells with MoAb prior to their iv injection into normal animals results in a significant increase of pulmonary metastatic nodules.
在用识别180,000道尔顿细胞表面肿瘤相关蛋白的单克隆抗体(MoAb)135-13C处理分离的肿瘤细胞或荷瘤动物后,对Lewis肺癌的生长和扩散进行了分析。本研究结果表明,MoAb 135-13C与Lewis肺癌肿瘤细胞具有高亲和力结合,并对原发性肿瘤(肿瘤重量降低20%-25%)及其转移(肺结节形成增加两倍)产生不同影响。不同的MoAb 135-13C给药方案表明,这些影响具有剂量和时间依赖性。特别是,当在全身肿瘤播散时给予MoAb 135-13C时,观察到转移形成的最大增加。在将肿瘤细胞静脉注射到正常动物体内之前,先用MoAb进行体外预孵育,会导致肺转移结节显著增加。