Clinical considerations of CDK4/6 inhibitors in triple-negative breast cancer

The formation of cyclinD-CDK4/6 complex plays vital roles in the cell cycle transition from G1 phase to S phase which is characterized by vigorous transcription and synthesis. Through cyclinD-CDK4/6-Rb axis, CDK4/6 inhibitors arrest the cell cycle in the G1 phase and block the proliferation of aggressive cells, exhibiting promising effects in containing the aggressiveness of breast cancers. To date, there are three CDK4/6 inhibitors approved by the U.S. Food and Drug Administration in treating advanced hormone receptor-positive breast cancer, including palbociclib, abemaciclib, and ribociclib. In fact, several preclinical experiments and clinical trials presented therapeutic effects of CDK4/6 inhibitor-based treatment in triple-negative breast cancer.

Automated summary

The formation of cyclinD-CDK4/6 complex is essential for the cell cycle transition from G1 phase to S phase. CDK4/6 inhibitors can block cell cycle progression and proliferation, showing promising effects in containing the aggressiveness of breast cancers, particularly in triple-negative breast cancer.