癌细胞中转铁蛋白受体的抗体介导靶向

Rosendo Luria-Pérez , Gustavo Helguera , José A. Rodríguez
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引用次数: 0

摘要

铁对细胞生长至关重要,部分通过转铁蛋白(Tf)进入细胞,转铁蛋白与细胞表面的受体(TfR1或CD71)结合,然后将铁释放到核内体中。TfR1是一种单代ii型跨膜蛋白,在大多数组织中以基础水平表达。TfR1的高表达通常与快速增殖的细胞有关,包括各种类型的癌症。TfR1之所以成为实验治疗的靶点,有几个原因:它的细胞表面可及性、对细胞的组成性内吞作用、在细胞生长和增殖中的重要作用以及它在癌细胞中的过表达。在用于靶向TfR1的治疗剂中,抗体因其显著的特异性和亲和力而脱颖而出。目前正在进行临床试验,以评估针对TfR1的药物在癌症患者中的安全性和有效性,并取得了令人鼓舞的结果。这些观察结果表明,靶向TfR1作为直接治疗或递送管道的疗法仍然是治疗过表达受体的癌症的有吸引力的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibody-mediated targeting of the transferrin receptor in cancer cells

Iron is essential for cell growth and is imported into cells in part through the action of transferrin (Tf), a protein that binds its receptor (TfR1 or CD71) on the surface of a cell, and then releases iron into endosomes. TfR1 is a single pass type-II transmembrane protein expressed at basal levels in most tissues. High expression of TfR1 is typically associated with rapidly proliferating cells, including various types of cancer. TfR1 is targeted by experimental therapeutics for several reasons: its cell surface accessibility, constitutive endocytosis into cells, essential role in cell growth and proliferation, and its overexpression by cancer cells. Among the therapeutic agents used to target TfR1, antibodies stand out due to their remarkable specificity and affinity. Clinical trials are being conducted to evaluate the safety and efficacy of agents targeting TfR1 in cancer patients with promising results. These observations suggest that therapies targeting TfR1 as direct therapeutics or delivery conduits remain an attractive alternative for the treatment of cancers that overexpress the receptor.

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