Portman Neil, Chen Julia, Lim Elgene
Cancer Theme, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
St. Vincent's Clinical School, University of New South Wales (UNSW) Sydney, Kensington, NSW, Australia.
Front Oncol. 2021 Nov 3;11:777867. doi: 10.3389/fonc.2021.777867. eCollection 2021.
With the adoption of inhibitors of cyclin dependent kinases 4 and 6 (CDK4/6i) in combination with endocrine therapy as standard of care for the treatment of advanced and metastatic estrogen receptor positive (ER+) breast cancer, the search is now on for novel therapeutic options to manage the disease after the inevitable development of resistance to CDK4/6i. In this review we will consider the integral role that the p53/MDM2 axis plays in the interactions between CDK4/6, ERα, and inhibitors of these molecules, the current preclinical evidence for the efficacy of MDM2 inhibitors in ER+ breast cancer, and discuss the possibility of targeting the p53/MDM2 inhibition of MDM2 in the CDK4/6i resistance setting.
随着细胞周期蛋白依赖性激酶4和6抑制剂(CDK4/6i)与内分泌治疗联合应用成为晚期和转移性雌激素受体阳性(ER+)乳腺癌治疗的标准护理方案,目前正在寻找新的治疗选择,以应对对CDK4/6i不可避免产生耐药性后的疾病管理。在本综述中,我们将探讨p53/MDM2轴在CDK4/6、ERα以及这些分子抑制剂之间相互作用中所起的重要作用,MDM2抑制剂在ER+乳腺癌中疗效的当前临床前证据,并讨论在CDK4/6i耐药情况下靶向p53/MDM2抑制MDM2的可能性。