Amaral Joana D, Xavier Joana M, Steer Clifford J, Rodrigues Cecília M
Research Institute for Medicines and Pharmaceutical Sciences, Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.
Discov Med. 2010 Feb;9(45):145-52.
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.
p53的动态和多种功能,以及它与最常见的非传染性疾病的关联,凸显了阐明p53调控网络复杂性的必要性。诸如癌症、神经退行性变、缺血、胆汁淤积和动脉粥样硬化等病理状况都与凋亡失调密切相关,其中p53功能障碍起着重要作用。我们将重点介绍p53诱导的细胞凋亡在人类疾病中的最新进展,尤其关注肝细胞凋亡的调控。此外,我们还将讨论广泛激活p53作为癌症治疗方法所引发的争议。最近的研究提供了关于内源性胆汁酸熊去氧胆酸(UDCA)的机制性抗凋亡功能的相关且前所未有的信息,这表明Mdm-2(小鼠双微体2,一种癌蛋白)对p53的精细、复杂调控是UDCA调节p53触发的细胞凋亡的关键步骤。我们还将回顾靶向药物的最新治疗策略和临床应用、它们的安全性和有效性,特别强调UDCA的潜在益处。