RAS inhibitors: potential for cancer therapeutics

被引:75
作者
Kloog, Y [1 ]
Cox, AD
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Neurobiochem, IL-69978 Tel Aviv, Israel
[2] Univ N Carolina, Sch Med, Dept Radiat Oncol & Pharmacol, Chapel Hill, NC 27599 USA
来源
MOLECULAR MEDICINE TODAY | 2000年 / 6卷 / 10期
关键词
D O I
10.1016/S1357-4310(00)01789-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As RAS oncoproteins play a major role in human malignancy, inhibiting RAS function is a promising approach for developing anticancer therapies. Among these approaches are agents such as farnesyltransferase inhibitors (FTIs) and the nontoxic farnesylcysteine analogue farnesylthiosalicylic acid (FTS) that dislodges all RAS isoforms from the membrane, as well as methods to restore regulation of RAS-GTP levels and to alter the interaction of RAS-GTP with downstream targets.
引用
收藏
页码:398 / 402
页数:5
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