Department of Dermatology, The University of Alabama at Birmingham, Volker Hall, Room 509, 1530 3rd Avenue South, Birmingham, Alabama 35294-0019, USA.
Curr Pharm Des. 2011;17(6):631-9. doi: 10.2174/138161211795222595.
Tumor suppressor p53 is a transcription factor that regulates a large number of genes and guards against genomic instability. Under multiple cellular stress conditions, p53 functions to block cell cycle progression transiently unless proper DNA repair occurs. Failure of DNA repair mechanisms leads to p53-mediated induction of cell death programs. p53 also induces permanent cell cycle arrest known as cellular senescence. During neoplastic progression, p53 is often mutated and fails to efficiently perform these functions. It has been observed that cancers carrying a wild-type p53 may also have interrupted downstream p53 regulatory signaling leading to disruption in p53 functions. Therefore, strategies to reactivate p53 provide an attractive approach for blocking tumor pathogenesis and its progression. p53 activation may also lead to regression of existing early neoplastic lesions and therefore may be important in developing cancer chemoprevention protocols. A large number of small molecules capable of reactivating p53 have been developed and some are progressing through clinical trials for prospective human applications. However, several questions remain to be answered at this stage. For example, it is not certain if pharmacological activation of p53 will restore all of its multifaceted biological responses, assuming that the targeted cell is not killed following p53 activation. It remains to be demonstrated whether the distinct biological effects regulated by specific post-translationally modified p53 can effectively be restored by refolding mutant p53. Mutant p53 can be classified as a loss-of-function or gain-of-function protein depending on the type of mutation. It is also unclear whether reactivation of mutant p53 has similar consequences in cells carrying gain-of-function and loss-of-function p53 mutants. This review provides a description of various pharmacological approaches tested to activate p53 (both wild-type and mutant) and to assess the effects of activated p53 on neoplastic progression.
肿瘤抑制因子 p53 是一种转录因子,可调节大量基因并防止基因组不稳定。在多种细胞应激条件下,p53 的功能是暂时阻止细胞周期进程,除非发生适当的 DNA 修复。如果 DNA 修复机制失败,会导致 p53 介导的细胞死亡程序诱导。p53 还会诱导称为细胞衰老的永久性细胞周期停滞。在肿瘤进展过程中,p53 经常发生突变,无法有效地发挥这些功能。已经观察到携带野生型 p53 的癌症也可能中断下游 p53 调节信号,导致 p53 功能中断。因此,重新激活 p53 的策略为阻断肿瘤发病机制及其进展提供了一种有吸引力的方法。p53 的激活也可能导致现有早期肿瘤病变的消退,因此在开发癌症化学预防方案中可能很重要。已经开发出大量能够重新激活 p53 的小分子,其中一些正在临床试验中进行前瞻性人体应用。然而,在现阶段仍有一些问题需要回答。例如,尚不确定药理学激活 p53 是否会恢复其多方面的生物学反应,假设在 p53 激活后靶向细胞未被杀死。还需要证明由特定翻译后修饰的 p53 调节的不同生物学效应是否可以通过重新折叠突变型 p53 有效地恢复。突变型 p53 可根据突变类型分为失活功能或获得功能蛋白。也不清楚在携带获得功能和失活功能 p53 突变体的细胞中,重新激活突变型 p53 是否具有相似的后果。这篇综述描述了各种已测试的药理学方法来激活 p53(野生型和突变型),并评估激活的 p53 对肿瘤进展的影响。