生物
翻译后修饰
癌症
计算生物学
遗传学
生物化学
酶
作者
Yifat Geffen,Shankara Anand,Yo Akiyama,Tomer M. Yaron,Yizhe Song,Jared L. Johnson,Akshay Govindan,Özgün Babur,Yize Li,Emily M. Huntsman,Liang-Bo Wang,Chet Birger,David I. Heiman,Qing Zhang,Mendy Miller,Yosef E. Maruvka,Nicholas J. Haradhvala,Anna Calinawan,Saveliy Belkin,Alexander Kerelsky
出处
期刊:Cell
[Elsevier]
日期:2023-08-01
卷期号:186 (18): 3945-3967.e26
被引量:108
标识
DOI:10.1016/j.cell.2023.07.013
摘要
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.
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