Enzastaurin, a protein kinase cβ -: Selective inhibitor, and its potential application as an anticancer agent in lung cancer

被引:35
|
作者
Herbst, Roy S.
Oh, Yun
Wagle, Asavari
Lahn, Michael
机构
[1] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[2] Eli Lilly & Co, Indianapolis, IN 46285 USA
关键词
D O I
10.1158/1078-0432.CCR-07-0538
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Enzastaurin, an oral serine/threonine kinase inhibitor, suppresses signaling through protein kinase C (PKC) -beta and the phosphatidylinositol 3-kinase/AKT pathway to induce tumor cell apoptosis, reduce proliferation, and suppress tumor-induced angiogenesis. In contrast to previous PKC inhibitors, enzastaurin is very well tolerated with a favorable safety profile, allowing it to be dosed for extended durations. In the present review, we summarize the rationale for targeting PKC in cancer, the preclinical experience of enzastaurin, and the clinical findings of the current phase I and II studies. Based on the combined information, we present the rationale for its future assessment in the treatment of lung cancer.
引用
收藏
页码:4641S / 4646S
页数:6
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