Taveras Arthur G, Kirschmeier Paul, Baum Charles M
Department of Medicinal Chemistry, Schering-Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, New Jersey 07033, USA.
Curr Top Med Chem. 2003;3(10):1103-14. doi: 10.2174/1568026033452104.
Farnesyl Protein Transferase as a target for therapeutic intervention is currently under investigation in human clinical trials. Sch-66336 (sarasar), a benzocycloheptapyridyl Farnesyl Transferase Inhibitor (FTI), has been found to be effective in cellular proliferation assays and in in vivo oncology models both as a single agent and in combination with other anti-cancer agents. Clinically, early evidence is being generated that suggests efficacy in humans, particularly in patients with leukemia. Herein, we review the biology of FPT, the discovery of Sch-66336 and other benzocycloheptapyridyl FTIs, and the clinical evaluation of Sch-66336 for the treatment of leukemia and solid tumors.
法尼基蛋白转移酶作为治疗干预的靶点目前正在人类临床试验中进行研究。Sch-66336(sarasar)是一种苯并环庚吡啶基法尼基转移酶抑制剂(FTI),已发现在细胞增殖试验和体内肿瘤学模型中,无论是作为单一药物还是与其他抗癌药物联合使用都有效。临床上,早期证据表明其对人类有效,尤其是对白血病患者。在此,我们综述了法尼基蛋白转移酶(FPT)的生物学特性、Sch-66336和其他苯并环庚吡啶基FTIs的发现,以及Sch-66336治疗白血病和实体瘤的临床评估。