细胞凋亡
癌症研究
神经退行性变
熊去氧胆酸
胆汁酸
胆汁淤积
平方毫米
内生
生物
神经科学
生物信息学
医学
内科学
生物化学
内分泌学
疾病
作者
Joana D. Amaral,Joana M. Xavier,Clifford J. Steer,C.M.P. Rodrigues
出处
期刊:PubMed
日期:2010-02-01
卷期号:9 (45): 145-52
被引量:128
摘要
The dynamic and multiple functions of p53, together with its involvement in the most common non-infectious diseases, underscore the need to elucidate the complexity of the p53 regulatory networks. Pathological conditions such as cancer, neurodegeneration, ischemia, cholestasis, and atherosclerosis are all strongly associated with deregulated levels of apoptosis in which p53 dysfunction has a prominent role. We will highlight recent developments of p53-induced apoptosis in human diseases, with a focus on modulation of liver cell apoptosis. In addition, we will discuss controversies arising from widespread p53 activation as a therapeutic approach to cancer. Recent studies have provided relevant and unprecedented information about mechanistic antiapoptotic functions of the endogenous bile acid, ursodeoxycholic acid (UDCA), suggesting that the finely tuned, complex control of p53 by Mdm-2 (mouse double minute-2, an oncoprotein) is a key step in UDCA modulation of p53-triggered apoptosis. We will also review recent therapeutic strategies and clinical applications of targeted agents, their safety, and efficacy, with particular emphasis on potential benefits of UDCA.
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