生物
蛋白质基因组学
免疫疗法
免疫检查点
免疫
癌症
转录组
癌症免疫疗法
无容量
计算生物学
逃避(道德)
癌症研究
免疫学
遗传学
免疫系统
基因
基因表达
作者
Francesca Petralia,Weiping Ma,Tomer M. Yaron,Francesca Pia Caruso,Nicole Tignor,Joshua M. Wang,Daniel Charytonowicz,Jared L. Johnson,Emily M. Huntsman,Giacomo B. Marino,Anna Calinawan,John Erol Evangelista,Myvizhi Esai Selvan,Shrabanti Chowdhury,Dmitry Rykunov,Azra Krek,Xiaoyu Song,Berk Turhan,Karen E. Christianson,David A. Lewis
出处
期刊:Cell
[Cell Press]
日期:2024-02-01
卷期号:187 (5): 1255-1277.e27
被引量:76
标识
DOI:10.1016/j.cell.2024.01.027
摘要
Despite the successes of immunotherapy in cancer treatment over recent decades, less than <10%-20% cancer cases have demonstrated durable responses from immune checkpoint blockade. To enhance the efficacy of immunotherapies, combination therapies suppressing multiple immune evasion mechanisms are increasingly contemplated. To better understand immune cell surveillance and diverse immune evasion responses in tumor tissues, we comprehensively characterized the immune landscape of more than 1,000 tumors across ten different cancers using CPTAC pan-cancer proteogenomic data. We identified seven distinct immune subtypes based on integrative learning of cell type compositions and pathway activities. We then thoroughly categorized unique genomic, epigenetic, transcriptomic, and proteomic changes associated with each subtype. Further leveraging the deep phosphoproteomic data, we studied kinase activities in different immune subtypes, which revealed potential subtype-specific therapeutic targets. Insights from this work will facilitate the development of future immunotherapy strategies and enhance precision targeting with existing agents.
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