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WEE1 kinase limits CDK activities to safeguard DNA replication and mitotic entry.
- Source :
-
Mutation research [Mutat Res] 2020 Jan - Apr; Vol. 819-820, pp. 111694. Date of Electronic Publication: 2020 Feb 25. - Publication Year :
- 2020
-
Abstract
- Precise execution of the cell division cycle is vital for all organisms. The Cyclin dependent kinases (CDKs) are the main cell cycle drivers, however, their activities must be precisely fine-tuned to ensure orderly cell cycle progression. A major regulatory axis is guarded by WEE1 kinase, which directly phosphorylates and inhibits CDK1 and CDK2. The role of WEE1 in the G2/M cell-cycle phase has been thoroughly investigated, and it is a focal point of multiple clinical trials targeting a variety of cancers in combination with DNA-damaging chemotherapeutic agents. However, the emerging role of WEE1 in S phase has so far largely been neglected. Here, we review how WEE1 regulates cell-cycle progression highlighting the importance of this kinase for proper S phase. We discuss how its function is modulated throughout different cell-cycle stages and provide an overview of how WEE1 levels are regulated. Furthermore, we outline recent clinical trials targeting WEE1 and elaborate on the mechanisms behind the anticancer efficacy of WEE1 inhibition. Finally, we consider novel biomarkers that may benefit WEE1-inhibition approaches in the clinic.<br /> (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Subjects :
- Antineoplastic Agents therapeutic use
CDC2 Protein Kinase metabolism
Cell Cycle Proteins antagonists & inhibitors
Cell Cycle Proteins metabolism
Clinical Trials as Topic
Cyclin-Dependent Kinase 2 metabolism
DNA Damage
DNA Repair drug effects
DNA, Neoplasm metabolism
Humans
Mitosis drug effects
Molecular Targeted Therapy methods
Neoplasms drug therapy
Neoplasms enzymology
Neoplasms pathology
Protein Kinase Inhibitors therapeutic use
Protein-Tyrosine Kinases antagonists & inhibitors
Protein-Tyrosine Kinases metabolism
S Phase drug effects
S Phase genetics
Signal Transduction
CDC2 Protein Kinase genetics
Cell Cycle Proteins genetics
Cyclin-Dependent Kinase 2 genetics
DNA Replication drug effects
DNA, Neoplasm genetics
Gene Expression Regulation, Neoplastic
Neoplasms genetics
Protein-Tyrosine Kinases genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1873-135X
- Volume :
- 819-820
- Database :
- MEDLINE
- Journal :
- Mutation research
- Publication Type :
- Academic Journal
- Accession number :
- 32120135
- Full Text :
- https://doi.org/10.1016/j.mrfmmm.2020.111694