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- W2077890614 abstract "One of the hallmarks of cancer is genomic instability controlled by cell cycle checkpoints. The G1 and G2 checkpoints allow DNA damage responses, whereas the mitotic checkpoint enables correct seggregation of the sister chromosomes to prevent aneuploidy. Cancer cells often lack a functional G1 arrest and rely on G2 arrest for DNA damage responses. WEE1 kinase is an important regulator of the G2 checkpoint and is overexpressed in various cancer types. Inhibition of WEE1 is a promising strategy in cancer therapy in combination with DNA-damaging agents, especially when cancer cells harbor p53 mutations, as it causes mitotic catastrophy when DNA is not repaired during G2 arrest. Cancer cell response to WEE1 inhibition monotherapy has also been demonstrated in various types of cancer, including p53 wild-type cancers. We postulate that chromosomal instability can explain tumor response to WEE1 monotherapy. Therefore, chromosomal instability may need to be taken into account when determining the most effective strategy for the use of WEE1 inhibitors in cancer therapy." @default.
- W2077890614 created "2016-06-24" @default.
- W2077890614 creator A5053700204 @default.
- W2077890614 creator A5071336077 @default.
- W2077890614 creator A5082319404 @default.
- W2077890614 creator A5085918635 @default.
- W2077890614 date "2013-12-01" @default.
- W2077890614 modified "2023-10-18" @default.
- W2077890614 title "WEE1 inhibition and genomic instability in cancer" @default.
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- W2077890614 doi "https://doi.org/10.1016/j.bbcan.2013.05.002" @default.
- W2077890614 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23727417" @default.
- W2077890614 hasPublicationYear "2013" @default.
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