Rybak S M, Arndt M A E, Schirrmann T, Dübel S, Krauss J
Bionanomics, LLC, 411 Walnut Street, Green Cove Springs, FL 32043, USA.
Curr Pharm Des. 2009;15(23):2665-75. doi: 10.2174/138161209788923921.
Ribonucleases degrade RNA, now considered an important drug target. The parent member of this protein superfamily is bovine pancreatic RNase A that functions as a digestive enzyme. Other physiological roles and activities have been ascribed to more recently discovered members of this superfamily. Angiogenin was isolated by following angiogenic activity from cell culture media conditioned by colon cancer cells. ONCONASE kills tumor cells in vitro and in vivo and has advanced to a phase IIIb confirmatory clinical trial for the treatment of unresectable malignant mesothelioma. All three of these RNA degrading enzymes have been used to generate immunoRNases; chemical conjugates and ligand-RNase fusion proteins, for cancer therapy. The properties of each of these RNases are described along with the increasingly sophisticated construction of recombinant immunoRNases. The advantages of using RNase as an antibody payload is compared to using plant or bacterial toxins in the construction of immunotoxins, a related strategy for specifically killing malignant cells.
核糖核酸酶可降解RNA,目前它被视为一种重要的药物靶点。这个蛋白质超家族的母体成员是牛胰核糖核酸酶A,它作为一种消化酶发挥作用。该超家族中最近发现的成员具有其他生理作用和活性。血管生成素是通过追踪结肠癌细胞条件培养基中的血管生成活性而分离出来的。昂卡司他丁在体外和体内均能杀死肿瘤细胞,并且已进入治疗不可切除恶性间皮瘤的IIIb期确证性临床试验。这三种RNA降解酶都已被用于生成免疫核糖核酸酶,即化学偶联物和配体-核糖核酸酶融合蛋白,用于癌症治疗。文中描述了每种核糖核酸酶的特性以及重组免疫核糖核酸酶日益复杂的构建过程。将使用核糖核酸酶作为抗体有效载荷的优势与在构建免疫毒素(一种特异性杀死恶性细胞的相关策略)时使用植物或细菌毒素的优势进行了比较。