Tyrosine kinase inhibitors in preclinical development

被引:46
作者
Levitt, ML [1 ]
Koty, PP
机构
[1] Tel Aviv Univ, Sackler Sch Med, Chaim Sheba Med Ctr, Inst Oncol, IL-52621 Tel Hashomer, Israel
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Environm & Occupat Hlth, Pittsburgh, PA 15261 USA
关键词
protein tyrosine kinase antagonists; receptor protein tyrosine kinases; review; epidermal growth factor receptor; platelet derived growth factor receptor; Src tyrosine kinase;
D O I
10.1023/A:1006372102543
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Due to the limited efficacy of cytotoxic chemotherapy in the treatment of advanced malignancy and its excessive toxicity precluding its use in chemoprevention, new therapeutic and preventive strategies have been sought. One of the most interesting of these new approaches is the manipulation of signal transduction pathways. Among the approaches being considered to eventuate such a strategy is the inhibition of autophosphorylation, a critical first step in the signal transduction pathways of many cell surface receptor tyrosine kinases, as well as of non-receptor tyrosine kinases. This article is intended to review those tyrosine kinase inhibitors that are currently in preclinical development, for which there are data to support consideration for their use in chemoprevention or cancer treatment. We will focus upon those agents that have received attention in the past several years.
引用
收藏
页码:213 / 226
页数:14
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