Wernaart Demi, Fumagalli Amos, Agami Reuven
Division of Oncogenomics, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Erasmus MC, Department of Genetics, Rotterdam University, Rotterdam, The Netherlands.
Oncogene. 2024 Jun;43(27):2053-2062. doi: 10.1038/s41388-024-03069-2. Epub 2024 May 27.
The cancer peptidome has long been known to be altered by genetic mutations. However, more recently, non-genetic polypeptide mutations have also been related to cancer cells. These non-genetic mutations occur post-t30ranscriptionally, leading to the modification of the peptide primary structure, while the corresponding genes remain unchanged. Three main processes participate in the production of these aberrant proteins: mRNA alternative splicing, mRNA editing, and mRNA aberrant translation. In this review, we summarize the molecular mechanisms underlying these processes and the recent findings on the functions of the aberrant proteins, as well as their exploitability as new therapeutic targets due to their specific enrichment in cancer cells. These non-genetic aberrant polypeptides represent a source of novel cancer cell targets independent from their level of mutational burden, still to be exhaustively explored.
长期以来,人们一直认为癌症肽组会因基因突变而发生改变。然而,最近非遗传多肽突变也与癌细胞有关。这些非遗传突变发生在转录后,导致肽一级结构的修饰,而相应的基因保持不变。三个主要过程参与了这些异常蛋白质的产生:mRNA可变剪接、mRNA编辑和mRNA异常翻译。在这篇综述中,我们总结了这些过程背后的分子机制以及关于异常蛋白质功能的最新发现,以及由于它们在癌细胞中的特异性富集而作为新治疗靶点的可利用性。这些非遗传异常多肽代表了一种独立于其突变负担水平的新型癌细胞靶点来源,仍有待深入探索。