Fatty acid synthase inhibitors: new directions for oncology

被引:82
作者
Kridel, Steven J. [1 ]
Lowther, W. Todd [1 ]
Pemble, Charles W. [1 ]
机构
[1] Wake Forest Univ, Med Ctr, Sch Med, Dept Canc Biol, Winston Salem, NC 27157 USA
关键词
C75; cerulenin; fatty acid synthesis; flavonoids; inhibitor; metabolism; orlistat; thiolactomycin;
D O I
10.1517/13543784.16.11.1817
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Fatty acid synthase (FASN) is the enzyme that catalyzes the de novo synthesis of fatty acids in cells. Because of the strong expression in many cancers, FASN is an attractive and tractable target for therapeutic intervention. The discovery and development of pharmacologic agents that block FASN activity highlight the promise of these anticancer compounds. FASN inhibitors have also proven to be invaluable in developing a better understanding of the contribution of FASN and fatty acid synthesis to tumor cells. Recent advances in the development of crystal structures of FASN have provided promise towards the development of novel FASN inhibitors. This review outlines the preclinical development of FASN inhibitors, their antitumor effects and the strategies underway to develop novel inhibitors.
引用
收藏
页码:1817 / 1829
页数:13
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