Chène Patrick
Novartis, K125 443, CH-4002 Basel, Switzerland.
Nat Rev Cancer. 2003 Feb;3(2):102-9. doi: 10.1038/nrc991.
p53 is an attractive therapeutic target in oncology because its tumour-suppressor activity can be stimulated to eradicate tumour cells. Inhibiting the p53-MDM2 interaction is a promising approach for activating p53, because this association is well characterized at the structural and biological levels. MDM2 inhibits p53 transcriptional activity, favours its nuclear export and stimulates its degradation, so inhibiting the p53-MDM2 interaction with synthetic molecules should lead to p53-mediated cell-cycle arrest or apoptosis in p53-positive stressed cells.
p53是肿瘤学中一个有吸引力的治疗靶点,因为其肿瘤抑制活性可以被激活以根除肿瘤细胞。抑制p53与MDM2的相互作用是激活p53的一种有前景的方法,因为这种关联在结构和生物学水平上已得到充分表征。MDM2抑制p53的转录活性,促进其核输出并刺激其降解,因此用合成分子抑制p53与MDM2的相互作用应该会导致p53阳性应激细胞中p53介导的细胞周期停滞或凋亡。