p53 and the regulation of hepatocyte apoptosis: implications for disease pathogenesis

被引:39
作者
Amaral, Joana D. [1 ]
Castro, Rui E. [1 ]
Steer, Clifford J. [2 ,3 ]
Rodrigues, Cecilia M. P. [1 ]
机构
[1] Univ Lisbon, Fac Pharm, Res Inst Med & Pharmaceut Sci, P-1699 Lisbon, Portugal
[2] Univ Minnesota, Sch Med, Dept Med & Genet, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Cell Biol & Dev, Minneapolis, MN 55455 USA
关键词
ACID-INDUCED APOPTOSIS; PRIMARY BILIARY-CIRRHOSIS; CYTOCHROME-C RELEASE; TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION; TELOMERE-DYSFUNCTIONAL MICE; SMALL-MOLECULE INHIBITORS; PRIMARY RAT HEPATOCYTES; TUMOR-SUPPRESSOR P53; WILD-TYPE P53; URSODEOXYCHOLIC ACID;
D O I
10.1016/j.molmed.2009.09.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interplay between p53 and apoptosis in diseases such as cancer, neurodegeneration, ischemia and atherosclerosis underscores the need to understand the complexity of p53 networks. Here, we highlight recent studies of p53-induced apoptosis in human diseases, with a focus on the modulation of liver cell apoptosis. In addition, recent work has provided new insights into mechanisms underlying the antiapoptotic functions of the endogenous bile acid ursodeoxycholic acid (UDCA), suggesting that the finely tuned, complex control of p53 by Mdm2 is a key step in the UDCA modulation of deregulated, p53-triggered apoptosis. The effect of targeting cell death signaling proteins has been established in preclinical models of human diseases. Finally, we review recent therapeutic strategies and clinical applications of targeted agents, with a particular emphasis on the potential use of UDCA.
引用
收藏
页码:531 / 541
页数:11
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