Mossakowski Medical Research Institute PAS, Warsaw, Poland.
Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Cell Death Dis. 2024 Aug 31;15(8):638. doi: 10.1038/s41419-024-06965-3.
The major driver oncogenes MYC, mutant KRAS, and mutant TP53 often coexist and cooperate to promote human neoplasia, which results in anticancer therapeutic opportunities within their downstream molecular programs. However, little research has been conducted on whether redundancy and competition among oncogenes affect their programs and ability to drive neoplasia. By CRISPR‒Cas9-mediated downregulation we evaluated the downstream proteomics and transcriptomics programs of MYC, mutant KRAS, and mutant TP53 in a panel of cell lines with either one or three of these oncogenes activated, in cancers of the lung, colon and pancreas. Using RNAi screening of the commonly activated molecular programs, we found a signature of three proteins - RUVBL1, HSPA9, and XPO1, which could be efficiently targeted by novel drug combinations in the studied cancer types. Interestingly, the signature was controlled by the oncoproteins in a redundant or competitive manner rather than by cooperation. Each oncoprotein individually upregulated the target genes, while upon oncogene co-expression each target was controlled preferably by a dominant oncoprotein which reduced the influence of the others. This interplay was mediated by redundant routes of target gene activation - as in the case of mutant KRAS signaling to c-Jun/GLI2 transcription factors bypassing c-Myc activation, and by competition - as in the case of mutant p53 and c-Myc competing for binding to target promoters. The global transcriptomics data from the cell lines and patient samples indicate that the redundancy and competition of oncogenic programs are broad phenomena, that may constitute even a majority of the genes dependent on oncoproteins, as shown for mutant p53 in colon and lung cancer cell lines. Nevertheless, we demonstrated that redundant oncogene programs harbor targets for efficient anticancer drug combinations, bypassing the limitations for direct oncoprotein inhibition.
致癌基因 MYC、突变型 KRAS 和突变型 TP53 是主要的驱动基因,它们通常共同存在并协同作用,促进人类肿瘤的发生,这为其下游分子途径中的抗癌治疗机会提供了依据。然而,关于致癌基因之间的冗余和竞争是否会影响它们的途径以及驱动肿瘤发生的能力,相关研究甚少。通过 CRISPR-Cas9 介导的下调,我们评估了这些致癌基因在肺、结肠和胰腺癌症的细胞系中,在一个或三个致癌基因被激活的情况下,下游蛋白质组学和转录组学程序。通过对常见激活的分子途径进行 RNAi 筛选,我们发现了一组由三种蛋白(RUVBL1、HSPA9 和 XPO1)组成的特征性蛋白,这些蛋白在研究的癌症类型中可以通过新型药物组合进行有效靶向。有趣的是,该特征以冗余或竞争的方式而非协同作用受致癌蛋白控制。每个致癌蛋白单独上调靶基因,而在致癌基因共表达时,每个靶基因主要受优势致癌蛋白控制,从而降低了其他致癌蛋白的影响。这种相互作用是通过靶基因激活的冗余途径介导的,例如突变型 KRAS 信号转导至 c-Jun/GLI2 转录因子,绕过 c-Myc 激活,以及竞争途径,例如突变型 p53 和 c-Myc 竞争与靶启动子结合。来自细胞系和患者样本的全局转录组学数据表明,致癌基因途径的冗余和竞争是广泛存在的现象,甚至可能构成依赖致癌蛋白的大多数基因,如在结肠和肺癌细胞系中观察到的突变型 p53 情况。然而,我们证明冗余的致癌基因途径具有高效抗癌药物组合的靶点,绕过了直接抑制致癌蛋白的局限性。