Sears Timothy, Carter Hannah
Bioinformatics and Systems Biology Program, University of California San Diego, La Jolla, California.
Moores Cancer Center, University of California San Diego, La Jolla, California.
Cancer Res. 2025 Feb 17;85(4):642-643. doi: 10.1158/0008-5472.CAN-24-4553.
Tumors utilize various mechanisms of HLA disruption in order to evade immunosurveillance. Previous computational tools have interrogated specific aspects of this process, yet a holistic picture of HLA LOH, transcriptomic suppression, and alternative splicing has remained challenging. In a recent Nature Genetics study, Puttick and colleagues introduced MHC Hammer, a robust computational toolkit designed to dissect the complexities of HLA disruptions that mediate immune evasion in cancer. By analyzing comprehensive genomic and transcriptomic data across several large cancer cohorts, the study highlights the prevalence of HLA disruptions, particularly alternative splicing events, across various tumor types and identifies HLA LOH as an important immune evasion mechanism during metastasis in lung adenocarcinoma.
肿瘤利用多种HLA破坏机制来逃避免疫监视。先前的计算工具已经探究了这一过程的特定方面,但对HLA基因杂合性缺失、转录组抑制和可变剪接的整体情况仍具有挑战性。在最近的一项《自然·遗传学》研究中,普蒂克及其同事引入了MHC Hammer,这是一个强大的计算工具包,旨在剖析介导癌症免疫逃逸的HLA破坏的复杂性。通过分析多个大型癌症队列的综合基因组和转录组数据,该研究突出了HLA破坏,特别是可变剪接事件在各种肿瘤类型中的普遍性,并确定HLA基因杂合性缺失是肺腺癌转移过程中的一种重要免疫逃逸机制。