Program in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia, PA, USA.
Department of Biochemistry and Molecular Biophysics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Oncogene. 2021 Jun;40(25):4281-4290. doi: 10.1038/s41388-021-01852-z. Epub 2021 Jun 8.
The TP53 gene continues to hold distinction as the most frequently mutated gene in cancer. Since its discovery in 1979, hundreds of research groups have devoted their efforts toward understanding why this gene is so frequently selected against by tumors, with the hopes of harnessing this information toward the improved therapy of cancer. The result is that this protein has been meticulously analyzed in tumor and normal cells, resulting in over 100,000 publications, with an average of 5000 papers published on p53 every year for the past decade. The journey toward understanding p53 function has been anything but straightforward; in fact, the field is notable for the numerous times that established paradigms not only have been shifted, but in fact have been shattered or reversed. In this review, we will discuss the manuscripts, or series of manuscripts, that have most radically changed our thinking about how this tumor suppressor functions, and we will delve into the emerging challenges for the future in this important area of research. It is hoped that this review will serve as a useful historical reference for those interested in p53, and a useful lesson on the need to be flexible in the face of established paradigms.
TP53 基因仍然是癌症中最常发生突变的基因。自 1979 年发现以来,数百个研究小组致力于研究为什么肿瘤如此频繁地选择对抗这种基因,希望利用这些信息来改善癌症的治疗。其结果是,该蛋白在肿瘤和正常细胞中进行了细致的分析,产生了超过 10 万篇出版物,在过去十年中,每年平均有 5000 篇关于 p53 的论文发表。对 p53 功能的理解之旅绝非一帆风顺;事实上,该领域以多次确立的范例不仅被改变,而且实际上被打破或逆转而闻名。在这篇综述中,我们将讨论最彻底改变我们对这种肿瘤抑制因子功能的看法的论文,或者说是一系列论文,并深入探讨该重要研究领域未来出现的新挑战。我们希望这篇综述能为那些对 p53 感兴趣的人提供有用的历史参考,并为面对既定范例时需要灵活性提供一个有用的教训。