Liu Yanbiao, Park Seohyun, Li Yan
School of Science, Auckland University of Technology, Auckland 1010, New Zealand.
Maurice Wilkins Centre, Auckland 1010, New Zealand.
Cancers (Basel). 2025 Jun 11;17(12):1941. doi: 10.3390/cancers17121941.
CDK4/6 inhibition represents a new generation of cancer therapies, targeting CDK4/6 complexes to induce cell cycle arrest in the G1 phase. These inhibitors have been widely used in combination with hormone receptor antagonists for treating ER+/HER2- breast cancer, achieving significant clinical success. Building on this progress, ongoing research explores novel combination therapies and expands the application of CDK4/6 inhibitors to other diseases. However, challenges remain, including variable cellular responses and the rapid development of drug resistance. Recent studies have uncovered new resistance mechanisms and their unexpected effects on cell metabolism, autophagy, and the tumor microenvironment beyond cell cycle arrest. This review provides a comprehensive overview of the mechanisms by which CDK4/6 inhibitors combat cancer and explores their potential for more effective and personalized treatment strategies.
细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制代表了新一代癌症疗法,其靶向CDK4/6复合物以诱导细胞周期在G1期停滞。这些抑制剂已广泛与激素受体拮抗剂联合用于治疗雌激素受体阳性/人表皮生长因子受体2阴性(ER+/HER2-)乳腺癌,并取得了显著的临床成功。在此进展的基础上,正在进行的研究探索新型联合疗法,并将CDK4/6抑制剂的应用扩展到其他疾病。然而,挑战依然存在,包括细胞反应的变异性和耐药性的快速发展。最近的研究发现了新的耐药机制及其对细胞代谢、自噬和肿瘤微环境的意外影响,而不仅仅是细胞周期停滞。本综述全面概述了CDK4/6抑制剂对抗癌症的机制,并探讨了其在更有效和个性化治疗策略方面的潜力。