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Not so WEE: Targeting G(2)/M to kill mesothelioma cells

It has been known for many years that manipulation of cell cycle checkpoint function represents one approach by which the toxicity of chemotherapy and of ionizing radiation can be increased in tumor cells.(1)(-)(3) In particular, abrogation of the G(2)/M checkpoint has been shown to enhance the leth...

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Detalles Bibliográficos
Autor principal: Dent, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979810/
https://www.ncbi.nlm.nih.gov/pubmed/24496096
http://dx.doi.org/10.4161/cbt.27851
Descripción
Sumario:It has been known for many years that manipulation of cell cycle checkpoint function represents one approach by which the toxicity of chemotherapy and of ionizing radiation can be increased in tumor cells.(1)(-)(3) In particular, abrogation of the G(2)/M checkpoint has been shown to enhance the lethality of a wide range of toxic stresses.(1)(-)(3) Inhibition of the G(2)/M checkpoint after chemotherapy/irradiation would result in tumor cells entering mitosis with damaged DNA, which would in turn result in loss of clonogenic survival (i.e., a lethal mitosis).