
The implementation of decisions affecting cell viability and proliferation is based on prompt detection of the issue to be addressed, formulation and transmission of a correct set of instructions and fidelity in the execution of orders. While the first and the last are purely mechanical processes relying on the faithful functioning of single proteins or macromolecular complexes (sensors and effectors), information is the real cue, with signal amplitude, duration, and frequency ultimately determining the type of response. The cellular response to DNA damage is no exception to the rule. In this review article we focus on DNA damage responses in G2 and Mitosis. First, we set the stage describing mitosis and the machineries in charge of assembling the apparatus responsible for chromosome alignment and segregation as well as the inputs that control its function (checkpoints). Next, we examine the type of issues that a cell approaching mitosis might face, presenting the impact of post-translational modifications (PTMs) on the correct and timely functioning of pathways correcting errors or damage before chromosome segregation. We conclude this essay with a perspective on the current status of mitotic signaling pathway inhibitors and their potential use in cancer therapy.
mitosis, 2716 Genetics (clinical), phosphorylation, 10061 Institute of Molecular Cancer Research, Mitosis, 610 Medicine & health, QH426-470, checkpoint, 1311 Genetics, Oncology, 1313 Molecular Medicine, Genetics, Molecular Medicine, DNA damage, cancer therapy, 570 Life sciences; biology, Phosphorylation, ubiquitylation, 610 Medicine & health, Genetics (clinical), DNA Damage
mitosis, 2716 Genetics (clinical), phosphorylation, 10061 Institute of Molecular Cancer Research, Mitosis, 610 Medicine & health, QH426-470, checkpoint, 1311 Genetics, Oncology, 1313 Molecular Medicine, Genetics, Molecular Medicine, DNA damage, cancer therapy, 570 Life sciences; biology, Phosphorylation, ubiquitylation, 610 Medicine & health, Genetics (clinical), DNA Damage
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 4 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
