Beyond DNA binding - a review of the potential mechanisms mediating quinacrine's therapeutic activities in parasitic infections, inflammation, and cancers

被引:113
作者
Ehsanian, Reza [1 ,2 ,3 ]
Van Waes, Carter [1 ]
Feller, Stephan M. [3 ]
机构
[1] Natl Inst Deafness & Other Commun Disorders, Tumor Biol Sect, Head & Neck Surg Branch, NIH, Bethesda, MD 20892 USA
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[3] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Dept Mol Oncol,Cell Signalling Grp, Oxford OX3 9DS, England
来源
CELL COMMUNICATION AND SIGNALING | 2011年 / 9卷
关键词
NF-KAPPA-B; SQUAMOUS-CELL CARCINOMA; PROSTAGLANDIN-E SYNTHASE; ARACHIDONIC-ACID RELEASE; IRRADIATED HUMAN FIBROBLASTS; MALIGNANT PLEURAL EFFUSIONS; MULTIDRUG-RESISTANCE; PHOSPHOLIPASE A(2); TOPOISOMERASE-II; IN-VITRO;
D O I
10.1186/1478-811X-9-13
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This is an in-depth review of the history of quinacrine as well as its pharmacokinetic properties and established record of safety as an FDA-approved drug. The potential uses of quinacrine as an anti-cancer agent are discussed with particular attention to its actions on nuclear proteins, the arachidonic acid pathway, and multi-drug resistance, as well as its actions on signaling proteins in the cytoplasm. In particular, quinacrine's role on the NF-kappa B, p53, and AKT pathways are summarized.
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页数:18
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