Proteasome inhibitors in lung cancer

被引:51
作者
Scagliotti, Giorgio [1 ]
机构
[1] Univ Turin, Dept Clin & Biol Sci, Thorac Oncol Unit, San Luigi Hosp, I-10043 Orbassano, Torino, Italy
关键词
bortezomib; combination therapy; docetaxel; NSCLC; 26S proteasome; SCLC;
D O I
10.1016/j.critrevonc.2005.12.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Proteasome inhibition is a novel therapeutic approach that is being investigated in non-small cell and small cell lung cancer (NSCLC and SCLC). Proteasome inhibition affects a range of intracellular signals and disrupts the levels of numerous proteins, causing apoptosis via multiple pathways. Importantly, malignant cells are more sensitive to proteasome inhibition than normal cells. A number of proteasome inhibitors have demonstrated activity in preclinical studies, both as single agents and in combination with conventional and novel antineoplastic agents. However, only bortezomib, a dipeptide boronic acid analog, has been investigated in lung cancer clinical trials, in which it has shown activity as a single agent and in combination regimens. Numerous preclinical and clinical studies are ongoing in both NSCLC and SCLC. Proteasome inhibition could potentially play a significant role in the future management of these conditions. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:177 / 189
页数:13
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