Abstract
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.Citation1-Citation3 In particular, abrogation of the G2/M checkpoint has been shown to enhance the lethality of a wide range of toxic stresses.Citation1-Citation3 Inhibition of the G2/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).
Disclosure of Potential Conflicts of Interest
No potential conflicts of interest were disclosed.
Acknowledgments
P Dent is funded by R01 DK52825.