Factors that determine cell fate in mitotically arrested cancer cells

Naghmana Ashraf¹Roaa Kassim²Edward Goldstein²Taylor Landfair²Clarissa G. Nuñez²Jeffrey B. Arterburn²Charles Bradley Shuster^2*

• ¹Baylor College of Medicine, Houston, United States
• ²New Mexico State University, Las Cruces, United States

Cancer cells display a high degree of heterogeneity in their responses to mitotic arrest, from apoptosis during mitosis to surviving mitotic failure and continuing to progress through the cell cycle. Thus, understanding the basis for this variation may prove valuable for developing more effective chemotherapeutic strategies. To determine whether signaling pathways associated with cell proliferation and survival influence cell fate responses to mitotic arrest, we asked whether inhibition of Phosphoinositide 3-kinase (PI3K) signaling affected apoptosis in cancer cells exposed to a Kinesin Spindle Protein (KSP) inhibitor. Dual inhibition of KSP and PI3K signaling induced apoptosis more effectively than mitotic arrest or PI3K pathway inhibition alone, and live cell imaging with probes for mitotic progression and apoptosis revealed that HeLa cells that died during mitotic slippage underwent apoptosis during prometaphase arrest, suggesting that PI3K inhibition dramatically shifted the dynamics of cell death. Similar potentiation of mitotic cell death could be detected in SiHa cells, whereas other cancer or non-transformed cell lines were not sensitized by PI3K inhibition. Expression of constitutively active Rap1, which modulates both cell adhesion and PI3K activity, significantly increased the duration of mitotic arrest in a PI3K-dependent manner. Moreover, activated Rap1 significantly increased the fraction of cells that slipped completely back into interphase prior to apoptotic cell death. Together, these results shed insights into possible mechanisms by which cells may evade cell death during mitotic delay and suggest a strategy to optimize antimitotic interventions.