Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA 02142, USA; Cancer Center and Department of Pathology, Massachusetts General Hospital, Boston, MA 02115, USA.
Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA 02142, USA.
Cell. 2023 Aug 31;186(18):3945-3967.e26. doi: 10.1016/j.cell.2023.07.013. Epub 2023 Aug 14.
Post-translational modifications (PTMs) play key roles in regulating cell signaling and physiology in both normal and cancer cells. Advances in mass spectrometry enable high-throughput, accurate, and sensitive measurement of PTM levels to better understand their role, prevalence, and crosstalk. Here, we analyze the largest collection of proteogenomics data from 1,110 patients with PTM profiles across 11 cancer types (10 from the National Cancer Institute's Clinical Proteomic Tumor Analysis Consortium [CPTAC]). Our study reveals pan-cancer patterns of changes in protein acetylation and phosphorylation involved in hallmark cancer processes. These patterns revealed subsets of tumors, from different cancer types, including those with dysregulated DNA repair driven by phosphorylation, altered metabolic regulation associated with immune response driven by acetylation, affected kinase specificity by crosstalk between acetylation and phosphorylation, and modified histone regulation. Overall, this resource highlights the rich biology governed by PTMs and exposes potential new therapeutic avenues.
翻译后修饰(PTMs)在调节正常细胞和癌细胞的细胞信号传导及生理过程中发挥着关键作用。质谱技术的进步使得能够高通量、准确且灵敏地测量PTM水平,从而更好地理解它们的作用、普遍性及相互作用。在此,我们分析了来自1110例患有11种癌症类型(其中10种来自美国国立癌症研究所的临床蛋白质组肿瘤分析联盟[CPTAC])且具有PTM图谱的患者的最大蛋白质基因组学数据集。我们的研究揭示了参与癌症标志性过程的蛋白质乙酰化和磷酸化变化的泛癌模式。这些模式揭示了不同癌症类型肿瘤的亚群,包括因磷酸化导致DNA修复失调的肿瘤、因乙酰化驱动与免疫反应相关的代谢调节改变的肿瘤、因乙酰化和磷酸化之间的相互作用影响激酶特异性的肿瘤以及修饰的组蛋白调节。总体而言,该资源突出了由PTMs支配的丰富生物学特性,并揭示了潜在的新治疗途径。