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PMID: 19568282 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Cell cycle kinases as therapeutic targets for cancer.

Nature reviews. Drug discovery ·Vol. 8 ·No. 7 ·2009-07-00 ·Pages 547-66

Lapenna S, Giordano A

Abstract

Several families of protein kinases orchestrate the complex events that drive the cell cycle, and their activity is frequently deregulated in hyperproliferative cancer cells. Although several molecules that inhibit cell cycle kinases have been developed and clinically screened as potential anticancer agents, none of these has been approved for commercial use and an effective strategy to specifically control malignant cell proliferation has yet to be established. However, recent genetic and biochemical studies have provided information about the requirement for certain cell cycle kinases by specific tumours and specialized tissue types. Here, we discuss the potential and limitations of established cell cycle kinases as targets in anticancer drug discovery as well as novel strategies for the design of new agents.

MeSH Terms
Animals Aurora Kinases Cell Cycle Cell Cycle Proteins/antagonists & inhibitors,chemistry Cyclin-Dependent Kinases/antagonists & inhibitors DNA Damage Humans Neoplasms/drug therapy Protein Kinase Inhibitors/therapeutic use Protein Serine-Threonine Kinases/antagonists & inhibitors,chemistry Proto-Oncogene Proteins/antagonists & inhibitors,chemistry Retinoblastoma-Like Protein p130/physiology Staurosporine/analogs & derivatives,therapeutic use
Chemicals
Cell Cycle Proteins Protein Kinase Inhibitors Proto-Oncogene Proteins Retinoblastoma-Like Protein p130 7-hydroxystaurosporine Aurora Kinases Protein Serine-Threonine Kinases polo-like kinase 1 Cyclin-Dependent Kinases Staurosporine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lapenna Silvia
Oncology Research Centre of Mercogliano, Mercogliano, Avellino, Italy. [email protected]
Giordano Antonio
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Article Info
Journal
Nature reviews. Drug discovery
Abbr.
Nat Rev Drug Discov
ISSN
1474-1784
Published
2009-07-00
Pages
547-66
Language
English
Region
England
NLM ID
101124171
Subset
IM
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