Girardini Javier E, Walerych Dawid, Del Sal Giannino
Molecular Oncology Group, Institute of Molecular and Cell Biology of Rosario, IBR-CONICET, Rosario, Argentina.
Subcell Biochem. 2014;85:41-70. doi: 10.1007/978-94-017-9211-0_3.
Following the initial findings suggesting a pro-oncogenic role for p53 point mutants, more than 30 years of research have unveiled the critical role exerted by these mutants in human cancer. A growing body of evidence, including mouse models and clinical data, has clearly demonstrated a connection between mutant p53 and the development of aggressive and metastatic tumors. Even if the molecular mechanisms underlying mutant p53 activities are still the object of intense scrutiny, it seems evident that full activation of its oncogenic role requires the functional interaction with other oncogenic alterations. p53 point mutants, with their pleiotropic effects, simultaneously activating several mechanisms of aggressiveness, are engaged in multiple cross-talk with a variety of other cancer-related processes, thus depicting a complex molecular landscape for the mutant p53 network. In this chapter revealing evidence illustrating different ways through which this cooperation may be achieved will be discussed. Considering the proposed role for mutant p53 as a driver of cancer aggressiveness, disarming mutant p53 function by uncoupling the cooperation with other oncogenic alterations, stands out as an exciting possibility for the development of novel anti-cancer therapies.
在最初的研究结果表明p53点突变体具有促癌作用之后,三十多年的研究揭示了这些突变体在人类癌症中发挥的关键作用。越来越多的证据,包括小鼠模型和临床数据,清楚地证明了突变型p53与侵袭性和转移性肿瘤的发生之间存在联系。即使突变型p53活性的分子机制仍然是深入研究的对象,但很明显,其致癌作用的完全激活需要与其他致癌改变进行功能相互作用。具有多效性作用、同时激活多种侵袭机制的p53点突变体,与多种其他癌症相关过程进行多种相互作用,从而描绘出突变型p53网络复杂的分子图景。在本章中,将讨论揭示说明这种合作可能实现的不同方式的证据。考虑到突变型p53作为癌症侵袭驱动因素的假定作用,通过解除与其他致癌改变的合作来消除突变型p53的功能,作为开发新型抗癌疗法的一种令人兴奋的可能性而凸显出来。