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首页> 外文期刊>Journal of Cancer Therapy >Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/CD320 Is Effective in Targeting and Destroying Cancer Cells
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Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/CD320 Is Effective in Targeting and Destroying Cancer Cells

机译:皂素结合的跨钴胺素受体TCblR / CD320单克隆抗体可有效靶向和消灭癌细胞

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摘要

Cobalamin uptake into cells is mediated by the CD320 receptor for transcobalamin-bound cobalamin. Optimum receptor expression is associated with proliferating cells and therefore, in many cancers this receptor expression is up regulated. Delivering drugs or toxins via this receptor provides increased targeting to cancer cells while minimizing toxicity to the normal tissues. Saporin conjugated monoclonal antibodies to the extracellular domain of TCblR were effectively internalized to deliver a toxic dose of Saporin to some cancer cell lines propagating in culture. Antibody concentration of 2.5 nM was effective in producing optimum inhibition of cell proliferation. The cytotoxic effect of mAb-Saporin appears to be dictated primarily by the level of receptor expression and therefore normal primary cells expressing low levels of CD320 were spared while tumor cell lines with higher CD320 expression were destroyed. Targeting the pathway for cellular uptake of vitamin B12 via the CD320 receptor with toxin-antibody conjugates appears to be a viable treatment strategy for certain cancers that over expresses this receptor.
机译:钴胺素被细胞内结合钴胺素的CD320受体介导摄取钴胺素。最佳受体表达与增殖细胞有关,因此,在许多癌症中,该受体表达被上调。通过该受体递送药物或毒素可增加对癌细胞的靶向性,同时将对正常组织的毒性降至最低。有效地内化了针对TCblR胞外域的结合Saporin的单克隆抗体,以将毒性剂量的Saporin递送至在培养中繁殖的某些癌细胞系。 2.5 nM的抗体浓度可有效抑制细胞增殖。 mAb-Saporin的细胞毒性作用似乎主要由受体表达水平决定,因此可以节省表达低水平CD320的正常原代细胞,而破坏具有较高CD320表达的肿瘤细胞系。使用毒素抗体偶联物靶向通过CD320受体吸收维生素B12的细胞途径似乎是某些过度表达该受体的癌症的可行治疗策略。

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