Division of Surgery and Oncology, University of Liverpool, 5th Fl. UCD Building, Daulby St, Liverpool, L69 3GA, UK.
Curr Pharm Des. 2011;17(6):618-30. doi: 10.2174/138161211795222568.
p53, the "guardian of the genome" and the most mutated gene in cancer presents a considerable therapeutic opportunity as well as a challenge. In the past decade, several therapeutic strategies have been developed that aim to take advantage of a wealth of knowledge about p53, including insights into the biology and patho-biology of p53. Nevertheless, considerable challenges remain, not least as a result of tissue- and cancer-specific differences in p53 regulation and/or function. p53 does not act in the same manner in all tissues or in the cancers arising from them. Nor is p53 regulated in the same way in the wide variety of tissues from which cancers develop. Therefore, potential strategies for therapeutic targeting need to be tailored to each tumour/tissue type. This review summarises some of these tissue- and cancer-specific issues to suggest how different strategies are required for cancers arising from different tissues and to illustrate the complexities of therapeutic targeting of p53.
p53,作为“基因组的守护者”和癌症中突变最多的基因,为治疗提供了巨大的机会,同时也带来了挑战。在过去的十年中,已经开发了几种治疗策略,旨在利用大量关于 p53 的知识,包括对 p53 的生物学和病理生物学的深入了解。然而,仍然存在相当大的挑战,尤其是由于组织和癌症中 p53 调节和/或功能的特异性差异。p53 在所有组织或源自它们的癌症中并不以相同的方式发挥作用。在从各种组织中发展而来的癌症中,p53 的调节方式也不相同。因此,治疗靶向的潜在策略需要针对每种肿瘤/组织类型进行调整。这篇综述总结了一些这些组织和癌症特异性问题,以表明不同组织来源的癌症需要不同的策略,并说明靶向治疗 p53 的复杂性。