首页> 美国卫生研究院文献>British Journal of Cancer >Antigenicity and drug susceptibility of human osteogenic sarcoma cells escaping a cytotoxic methotrexate-albumin-monoclonal antibody conjugate.
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Antigenicity and drug susceptibility of human osteogenic sarcoma cells escaping a cytotoxic methotrexate-albumin-monoclonal antibody conjugate.

机译:人成骨肉瘤细胞的抗原性和药敏性逃脱了细胞毒性的甲氨蝶呤-白蛋白-单克隆抗体偶联物。

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摘要

Cells of osteogenic sarcoma line 791T were treated in vitro with a selectively cytotoxic methotrexate-human serum albumin-monoclonal antibody conjugate at concentrations which were toxic but allowed the "escape" of a small number of tumour cell colonies (less than 0.3% compared with controls). These colonies were propagated as clones in order to test their expression of the monoclonal antibody ( 791T /36)-defined antigen and their resistance to methotrexate (MTX) by comparison with parental cells. Most of the conjugate-treated clones were incapable of prolonged growth and died out, in contrast to untreated 791T clones which virtually always grow progressively. Only four treated clones grew at rates comparable with the parental line. Flow cytofluorometric analysis indicated that the surviving clones expressed normal or enhanced amounts of 791T /36-defined antigen and clonogenic assays demonstrated that they were sensitive to cytotoxicity by MTX. As could be predicted from these results, further exposure to the conjugate inhibited growth of the clones at doses comparable with those active against parental 791T cells. It is concluded that tumour cell clones emerging after exposure to a toxic concentration of a drug-antibody conjugate are not necessarily modified resistant clones, but may have severely impaired long-term growth potential or be susceptible to further contact with the same conjugate.
机译:用选择性细胞毒性甲氨蝶呤-人血清白蛋白-单克隆抗体偶联物体外处理成骨肉瘤细胞株791T,其浓度有毒,但允许“逃逸”少量肿瘤细胞集落(与对照相比,少于0.3% )。这些菌落作为克隆繁殖,以通过与亲代细胞比较来测试其单克隆抗体(791T / 36)定义的抗原的表达及其对甲氨蝶呤(MTX)的抗性。与未经处理的791T克隆实际上一直在逐步生长相比,大多数经缀合物处理的克隆无法延长生长并消失。仅四个处理的克隆以与亲本系相当的速率生长。流式细胞术分析表明,存活的克隆表达正常或增强量的791T / 36定义的抗原,克隆形成试验表明它们对MTX的细胞毒性敏感。从这些结果可以预料到,进一步暴露于缀合物会以与对亲代791T细胞有活性的剂量相当的剂量抑制克隆的生长。结论是,暴露于毒性浓度的药物-抗体偶联物后出现的肿瘤细胞克隆不一定是修饰的抗性克隆,但可能会严重损害其长期生长潜力或易于与相同的偶联物进一步接触。

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