皂苷偶联抗转钴胺素受体TCblR/CD320单克隆抗体有效靶向和杀伤癌细胞

Edward V Quadros, Yasumi Nakayama, Jeffrey M Sequeira
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引用次数: 9

摘要

转钴胺结合钴胺素的CD320受体介导钴胺素摄取进入细胞。最佳受体表达与细胞增殖有关,因此,在许多癌症中,这种受体表达被上调。通过这种受体输送药物或毒素增加了对癌细胞的靶向性,同时将对正常组织的毒性降到最低。在体外培养繁殖的肿瘤细胞系中,有效地内化了TCblR胞外结构域的皂苷偶联单克隆抗体,以传递毒性剂量的皂苷。抗体浓度为2.5 nM时对细胞增殖的抑制效果最佳。mAb-Saporin的细胞毒性作用似乎主要取决于受体的表达水平,因此表达低水平CD320的正常原代细胞得以存活,而CD320表达高水平的肿瘤细胞系则被破坏。利用毒素抗体偶联物靶向CD320受体对维生素B12的细胞摄取途径似乎是一种可行的治疗策略,用于过度表达该受体的某些癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/<i>CD</i>320 Is Effective in Targeting and Destroying Cancer Cells.

Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/<i>CD</i>320 Is Effective in Targeting and Destroying Cancer Cells.

Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/<i>CD</i>320 Is Effective in Targeting and Destroying Cancer Cells.

Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/CD320 Is Effective in Targeting and Destroying Cancer Cells.

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.

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