Drug-repositioning opportunities for cancer therapy: novel molecular targets for known compounds

被引:113
|
作者
Wuerth, Roberto [1 ,2 ]
Thellung, Stefano [1 ,2 ]
Bajetto, Adriana [1 ,2 ]
Mazzanti, Michele [3 ]
Florio, Tullio [1 ,2 ]
Barbieri, Federica [1 ,2 ]
机构
[1] Univ Genoa, Dept Internal Med, Viale Benedetto 15, I-16132 Genoa, Italy
[2] Univ Genoa, CEBR, Viale Benedetto 15, I-16132 Genoa, Italy
[3] Univ Milan, Dept Biosci, I-20122 Milan, Italy
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; TUMOR-INITIATING CELLS; BREAST-CANCER; STEM-CELLS; IN-VITRO; PANCREATIC-CANCER; COMBINATION CHEMOTHERAPY; METFORMIN DECREASES; ANTICANCER AGENT; BROAD-SPECTRUM;
D O I
10.1016/j.drudis.2015.09.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug repositioning is gaining increasing attention in drug discovery because it represents a smart way to exploit new molecular targets of a known drug or target promiscuity among diverse diseases, for medical uses different from the one originally considered. In this review, we focus on known non-oncological drugs with new therapeutic applications in oncology, explaining the rationale behind this approach and providing practical evidence. Moving from incompleteness of the knowledge of drug-target interactions, particularly for older molecules, we highlight opportunities for repurposing compounds as cancer therapeutics, underling the biologically and clinically relevant affinities for new targets. Ideal candidates for repositioning can contribute to the therapeutically unmet need for more-efficient anticancer agents, including drugs that selectively target cancer stem cells.
引用
收藏
页码:190 / 199
页数:10
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