Krauss Jürgen, Arndt Michaela A E, Dübel Stefan, Rybak Susanna M
Natinal center for tumor diseases (NCT), Universit6y of Heidelberg, Im Neuenheimer Fild 350, D-69120 Heidleberg, Germany.
Curr Pharm Biotechnol. 2008 Jun;9(3):231-4. doi: 10.2174/138920108784567317.
Ribonucleases (RNases) of the superfamily A exhibit potent antineoplastic activity yet do not mediate appreciable immunogenicity or non-specific toxicity in both animal models and cancer patients. Ranpirnase (Onconase), the first ribonuclease being evaluated as a therapeutic in humans, has progressed to phase III clinical trials in patients with unresectable mesothelioma. Conjugation of RNases to internalizing tumor-targeting monoclonal antibodies was shown to enhance specific cell killing by several orders of magnitude both in vitro and in animal models. In this review we describe the development and current status of genetically engineered 2(nd) generation immunoRNases as promising novel anti-cancer therapeutics.
A超家族的核糖核酸酶(RNases)具有强大的抗肿瘤活性,但在动物模型和癌症患者中均未介导明显的免疫原性或非特异性毒性。兰瑞肽酶(Onconase)是首个被评估用于人类治疗的核糖核酸酶,已进入不可切除间皮瘤患者的III期临床试验。在体外和动物模型中,将RNases与内化肿瘤靶向单克隆抗体偶联可使特异性细胞杀伤增强几个数量级。在本综述中,我们描述了作为有前景的新型抗癌疗法的基因工程第二代免疫核糖核酸酶的研发情况和现状。