Baum Charles, Kirschmeier Paul
Schering-Plough Research Institute, 2015 Galloping Hill Road, K-15-3-3200, Kenilworth, NJ 07033-1300, USA.
Curr Oncol Rep. 2003 Mar;5(2):99-107. doi: 10.1007/s11912-003-0096-5.
Farnesylation of Ras, a protooncogene that is frequently mutated in a number of malignancies, is critical for its biologic function. This observation has led to the development of several agents that inhibit farnesyltransferase, known as farnesyltransferase inhibitors (FTIs). The antiproliferative and antitumor effects of these agents have been demonstrated in preclinical and clinical studies. Interestingly, FTI activity does not necessarily rely on ras mutational status, indicating that Ras is not the only FTI target. Clinical data suggest that FTIs, alone and in combination with other agents, have antitumor activity. Further study is needed to determine the precise mechanism of FTI antitumor activity as well as how and where FTIs will be best used clinically.
Ras是一种原癌基因,在许多恶性肿瘤中经常发生突变,其法尼基化对于其生物学功能至关重要。这一发现促使了几种抑制法尼基转移酶的药物的开发,即法尼基转移酶抑制剂(FTIs)。这些药物的抗增殖和抗肿瘤作用已在临床前和临床研究中得到证实。有趣的是,FTI活性不一定依赖于ras突变状态,这表明Ras不是FTI的唯一靶点。临床数据表明,FTIs单独使用或与其他药物联合使用均具有抗肿瘤活性。需要进一步研究以确定FTI抗肿瘤活性的确切机制,以及FTIs在临床上的最佳使用方式和地点。