Biotherapy Section, Laboratory of Molecular Biology, Center of Cancer Research, National Cancer Institute, NIH., 37 Convent Dr, Room 5124, Bethesda, MD 20892, USA.
Biomolecules. 2020 Sep 17;10(9):1331. doi: 10.3390/biom10091331.
Cancer cells frequently upregulate surface receptors that promote growth and survival. These receptors constitute valid targets for intervention. One strategy involves the delivery of toxic payloads with the goal of killing those cancer cells with high receptor levels. Delivery can be accomplished by attaching a toxic payload to either a receptor-binding antibody or a receptor-binding ligand. Generally, the cell-binding domain of the toxin is replaced with a ligand or antibody that dictates a new binding specificity. The advantage of this "immunotoxin" approach lies in the potency of these chimeric molecules for killing cancer cells. However, receptor expression on normal tissue represents a significant obstacle to therapeutic intervention.
癌细胞经常上调促进生长和存活的表面受体。这些受体是干预的有效靶点。一种策略涉及用有毒有效负载进行递送,目的是杀死那些受体水平高的癌细胞。通过将有毒有效负载连接到受体结合抗体或受体结合配体上,可以实现递送。通常,毒素的细胞结合结构域被替换为决定新结合特异性的配体或抗体。这种“免疫毒素”方法的优势在于这些嵌合分子对杀伤癌细胞的效力。然而,正常组织上的受体表达是治疗干预的一个重大障碍。