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Recent Findings and Future Directions for Interpolar Mitotic Kinesin Inhibitors in Cancer Therapy

Overview
Journal Future Med Chem
Specialties Chemistry
Pharmacy
Date 2016 Mar 16
PMID 26976726
Citations 42
Authors
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Abstract

The kinesin class of microtubule-associated motor proteins present attractive anticancer targets owing to their roles in key functions in dividing cells. Two interpolar mitotic kinesins Eg5 and HSET have opposing motor functions in mitotic spindle assembly with respect to microtubule movement, but both offer opportunities to develop cancer selective therapeutic agents. Here, we summarize the progress to date in developing inhibitors of Eg5 and HSET, with an emphasis on structural biology insights into the binding modes of allosteric inhibitors, compound selectivity and mechanisms of action of different chemical scaffolds. We discuss translation of preclinical studies to clinical experience with Eg5 inhibitors, recent findings on potential resistance mechanisms and explore the implications for future anticancer drug development against these targets.

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References
1.
Cross R, McAinsh A . Prime movers: the mechanochemistry of mitotic kinesins. Nat Rev Mol Cell Biol. 2014; 15(4):257-71. DOI: 10.1038/nrm3768. View

2.
Matsuno K, Sawada J, Sugimoto M, Ogo N, Asai A . Bis(hetero)aryl derivatives as unique kinesin spindle protein inhibitors. Bioorg Med Chem Lett. 2009; 19(4):1058-61. DOI: 10.1016/j.bmcl.2009.01.018. View

3.
Sun D, Lu J, Ding K, Bi D, Niu Z, Cao Q . The expression of Eg5 predicts a poor outcome for patients with renal cell carcinoma. Med Oncol. 2013; 30(1):476. DOI: 10.1007/s12032-013-0476-0. View

4.
Komlodi-Pasztor E, Sackett D, Tito Fojo A . Inhibitors targeting mitosis: tales of how great drugs against a promising target were brought down by a flawed rationale. Clin Cancer Res. 2012; 18(1):51-63. DOI: 10.1158/1078-0432.CCR-11-0999. View

5.
Bender A, Young D, Jenkins J, Serrano M, Mikhailov D, Clemons P . Chemogenomic data analysis: prediction of small-molecule targets and the advent of biological fingerprint. Comb Chem High Throughput Screen. 2007; 10(8):719-31. DOI: 10.2174/138620707782507313. View