Senter P D
Oncogen, Seattle, Washington 98121.
FASEB J. 1990 Feb 1;4(2):188-93. doi: 10.1096/fasebj.4.2.2404820.
A new strategy for the delivery of cytotoxic agents to solid tumors is described in which monoclonal antibodies are used as carriers for enzymes to tumor cell surfaces. The enzymes are chosen for their abilities to convert relatively noncytotoxic drug precursors (pro-drugs) into active anticancer drugs. The drugs thus formed can then penetrate into nearby tumor cells, resulting in cell death. A number of prodrugs have been developed that can be transformed into active anti-cancer drugs by enzymes of both mammalian and non-mammalian origin. The enzymes have been shown to localize into tumors when linked to monoclonal antibodies that bind to tumor-associated antigens. In vivo studies indicate that MAb-enzyme/prodrug combinations can result in antitumor activities significantly greater than those of the prodrugs or drugs given alone. This is most likely due to the generation of large amounts of active drug at the tumor site.
本文描述了一种将细胞毒性药物递送至实体瘤的新策略,该策略利用单克隆抗体作为酶载体,将其输送到肿瘤细胞表面。选择这些酶是因为它们能够将相对无细胞毒性的药物前体(前药)转化为活性抗癌药物。由此形成的药物随后可渗透到附近的肿瘤细胞中,导致细胞死亡。已经开发出多种前药,它们可被源自哺乳动物和非哺乳动物的酶转化为活性抗癌药物。当这些酶与结合肿瘤相关抗原的单克隆抗体相连时,已显示它们能在肿瘤中定位。体内研究表明,单克隆抗体-酶/前药组合产生的抗肿瘤活性明显高于单独给予前药或药物时的活性。这很可能是由于在肿瘤部位产生了大量活性药物。