Targeting MDM2 for the development of a new cancer therapy: progress and challenges

被引:1
|
作者
Aguilar, Angelo [1 ]
Thomas, Junius E. [1 ,2 ]
Wang, Shaomeng [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Program Chem Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Med Chem, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Rogel Canc Ctr, Ann Arbor, MI 48109 USA
关键词
MDM2-p53; inhibitors; Cancer therapy; Clinical trials; Combination therapy; Degraders; Intermittent dosing; PHASE-I; PROTEIN-DEGRADATION; P53; PATHWAY; AMG; 232; INHIBITOR; DISCOVERY; POTENT; ACTIVATION; SAR405838; COMPLEX;
D O I
10.1007/s00044-023-03102-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
For much of the past 20 years, MDM2 has been pursued as a cancer therapeutic target. Small molecule inhibitors that block the MDM2-p53 protein-protein interaction (MDM2 inhibitors) have been developed and a number of them have been evaluated in clinical trials for cancer treatment. Notwithstanding various setbacks, several MDM2 inhibitors have now progressed into late-stage clinical development. New strategies have also been developed to enhance the efficacy of MDM2 inhibitors and to mitigate their on-target toxicity. In this review, we summarize the progress and challenges in the development of a MDM2 targeted therapy.
引用
收藏
页码:1334 / 1344
页数:11
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