Li Zhen, Zou Wei, Zhang Ji, Zhang Yunjiao, Xu Qi, Li Siyuan, Chen Ceshi
Department of the Third Breast Surgery, The Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Queen Mary Institute, Nanchang University, Nanchang, China.
Front Pharmacol. 2020 Nov 16;11:580251. doi: 10.3389/fphar.2020.580251. eCollection 2020.
As a new-generation CDK inhibitor, a CDK4/6 inhibitor combined with endocrine therapy has been successful in the treatment of advanced estrogen receptor-positive (ER+) breast cancer. Although there has been overall progress in the treatment of cancer, drug resistance is an emerging cause for breast cancer-related death. Overcoming CDK4/6 resistance is an urgent problem. Overactivation of the cyclin-CDK-Rb axis related to uncontrolled cell proliferation is the main cause of CDK4/6 inhibitor resistance; however, the underlying mechanisms need to be clarified further. We review various resistance mechanisms of CDK4/6 inhibitors in luminal breast cancer. The cell signaling pathways involved in therapy resistance are divided into two groups: upstream response mechanisms and downstream bypass mechanisms. Finally, we discuss possible strategies to overcome CDK4/6 inhibitor resistance and identify novel resistance targets for future clinical application.
作为新一代细胞周期蛋白依赖性激酶(CDK)抑制剂,CDK4/6抑制剂联合内分泌治疗已成功用于晚期雌激素受体阳性(ER+)乳腺癌的治疗。尽管癌症治疗总体上取得了进展,但耐药性是导致乳腺癌相关死亡的一个新出现的原因。克服CDK4/6耐药性是一个紧迫的问题。与不受控制的细胞增殖相关的细胞周期蛋白-CDK-Rb轴过度激活是CDK4/6抑制剂耐药的主要原因;然而,其潜在机制仍需进一步阐明。我们综述了管腔型乳腺癌中CDK4/6抑制剂的各种耐药机制。参与治疗耐药的细胞信号通路分为两组:上游反应机制和下游旁路机制。最后,我们讨论了克服CDK4/6抑制剂耐药性的可能策略,并确定了未来临床应用的新的耐药靶点。