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- Publisher Website: 10.1016/j.molcel.2015.11.006
- Scopus: eid_2-s2.0-84947753819
- PMID: 26590712
- WOS: WOS:000368288700004
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Article: Targeting Mitosis in Cancer: Emerging Strategies
Title | Targeting Mitosis in Cancer: Emerging Strategies |
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Authors | |
Issue Date | 2015 |
Citation | Molecular Cell, 2015, v. 60, n. 4, p. 524-536 How to Cite? |
Abstract | © 2015 Elsevier Inc. The cell cycle is an evolutionarily conserved process necessary for mammalian cell growth and development. Because cell-cycle aberrations are a hallmark of cancer, this process has been the target of anti-cancer therapeutics for decades. However, despite numerous clinical trials, cell-cycle-targeting agents have generally failed in the clinic. This review briefly examines past cell-cycle-targeted therapeutics and outlines how experience with these agents has provided valuable insight to refine and improve anti-mitotic strategies. An overview of emerging anti-mitotic approaches with promising pre-clinical results is provided, and the concept of exploiting the genomic instability of tumor cells through therapeutic inhibition of mitotic checkpoints is discussed. We believe this strategy has a high likelihood of success given its potential to enhance therapeutic index by targeting tumor-specific vulnerabilities. This reasoning stimulated our development of novel inhibitors targeting the critical regulators of genomic stability and the mitotic checkpoint: AURKA, PLK4, and Mps1/TTK. |
Persistent Identifier | http://hdl.handle.net/10722/292915 |
ISSN | 2023 Impact Factor: 14.5 2023 SCImago Journal Rankings: 9.332 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Dominguez-Brauer, Carmen | - |
dc.contributor.author | Thu, Kelsie L. | - |
dc.contributor.author | Mason, Jacqueline M. | - |
dc.contributor.author | Blaser, Heiko | - |
dc.contributor.author | Bray, Mark R. | - |
dc.contributor.author | Mak, Tak W. | - |
dc.date.accessioned | 2020-11-17T14:57:29Z | - |
dc.date.available | 2020-11-17T14:57:29Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Molecular Cell, 2015, v. 60, n. 4, p. 524-536 | - |
dc.identifier.issn | 1097-2765 | - |
dc.identifier.uri | http://hdl.handle.net/10722/292915 | - |
dc.description.abstract | © 2015 Elsevier Inc. The cell cycle is an evolutionarily conserved process necessary for mammalian cell growth and development. Because cell-cycle aberrations are a hallmark of cancer, this process has been the target of anti-cancer therapeutics for decades. However, despite numerous clinical trials, cell-cycle-targeting agents have generally failed in the clinic. This review briefly examines past cell-cycle-targeted therapeutics and outlines how experience with these agents has provided valuable insight to refine and improve anti-mitotic strategies. An overview of emerging anti-mitotic approaches with promising pre-clinical results is provided, and the concept of exploiting the genomic instability of tumor cells through therapeutic inhibition of mitotic checkpoints is discussed. We believe this strategy has a high likelihood of success given its potential to enhance therapeutic index by targeting tumor-specific vulnerabilities. This reasoning stimulated our development of novel inhibitors targeting the critical regulators of genomic stability and the mitotic checkpoint: AURKA, PLK4, and Mps1/TTK. | - |
dc.language | eng | - |
dc.relation.ispartof | Molecular Cell | - |
dc.title | Targeting Mitosis in Cancer: Emerging Strategies | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1016/j.molcel.2015.11.006 | - |
dc.identifier.pmid | 26590712 | - |
dc.identifier.scopus | eid_2-s2.0-84947753819 | - |
dc.identifier.volume | 60 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | 524 | - |
dc.identifier.epage | 536 | - |
dc.identifier.eissn | 1097-4164 | - |
dc.identifier.isi | WOS:000368288700004 | - |
dc.identifier.issnl | 1097-2765 | - |