Cyclin-Dependent Kinase 4/6 Inhibitors Against Breast Cancer

Breast cancer is the most frequently diagnosed and leading cause of cancer-related deaths in women worldwide. Based on global cancer (GLOBOCAN) 2020 statistics, 1 in 4 cancer cases and 1 in 6 cancer deaths are attributable to breast cancer, leading both in incidence and mortality. To address the increasing burden of cancer, novel therapeutic approaches that target key hallmarks of cancer are explored in cancer drug discovery. Cyclin-dependent kinase (CDK) inhibitors are generally purine and pyrimidine analogues validated for the treatment of cancer due to their unique roles in cancer deregulation and novel therapeutic potentials. So far, three orally administered, potent and highly selective CDK4/6 inhibitors (palbociclib, ribociclib, abemaciclib) have been approved by the FDA for the targeted treatment of advanced or metastatic breast cancer in combination with endocrine therapy. Furthermore, several compounds derived from various synthetic scaffolds are being explored with promising results and positive outcomes in various stages of clinical trials. In this review, we highlight these CDK4/6 inhibitor compounds with potent anti-CDK4/6, in vitro and in vivo activities on breast cancer cells. With the remarkable prospects of these compounds, there is great optimism further novel CDK inhibitor compounds will be discovered in the future that could boost therapeutic options for cancer treatment.

Automated summary

Breast cancer is the leading cause of cancer-related deaths in women worldwide. FDA has approved three CDK4/6 inhibitors for the targeted treatment of advanced or metastatic breast cancer, and several compounds derived from various synthetic scaffolds are showing promising results in clinical trials. This review highlights the potent anti-CDK4/6 activities of these compounds and emphasizes the potential for discovering novel CDK inhibitor compounds in the future, expanding therapeutic options for cancer treatment.