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泛癌分析鉴定出来自转座元件的肿瘤特异性抗原。

Pan-cancer analysis identifies tumor-specific antigens derived from transposable elements.

作者信息

Shah Nakul M, Jang H Josh, Liang Yonghao, Maeng Ju Heon, Tzeng Shin-Cheng, Wu Angela, Basri Noah L, Qu Xuan, Fan Changxu, Li Amy, Katz Benjamin, Li Daofeng, Xing Xiaoyun, Evans Bradley S, Wang Ting

机构信息

Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.

The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Nat Genet. 2023 Apr;55(4):631-639. doi: 10.1038/s41588-023-01349-3. Epub 2023 Mar 27.

Abstract

Cryptic promoters within transposable elements (TEs) can be transcriptionally reactivated in tumors to create new TE-chimeric transcripts, which can produce immunogenic antigens. We performed a comprehensive screen for these TE exaptation events in 33 TCGA tumor types, 30 GTEx adult tissues and 675 cancer cell lines, and identified 1,068 TE-exapted candidates with the potential to generate shared tumor-specific TE-chimeric antigens (TS-TEAs). Whole-lysate and HLA-pulldown mass spectrometry data confirmed that TS-TEAs are presented on the surface of cancer cells. In addition, we highlight tumor-specific membrane proteins transcribed from TE promoters that constitute aberrant epitopes on the extracellular surface of cancer cells. Altogether, we showcase the high pan-cancer prevalence of TS-TEAs and atypical membrane proteins that could potentially be therapeutically exploited and targeted.

摘要

转座元件(TEs)中的隐匿性启动子可在肿瘤中被转录激活,从而产生新的TE嵌合转录本,这些转录本可产生免疫原性抗原。我们对33种TCGA肿瘤类型、30种GTEx成人组织和675个癌细胞系中的这些TE适应性事件进行了全面筛选,鉴定出1068个具有产生共享肿瘤特异性TE嵌合抗原(TS-TEAs)潜力的TE适应性候选物。全细胞裂解物和HLA下拉质谱数据证实TS-TEAs呈递在癌细胞表面。此外,我们强调了从TE启动子转录而来的肿瘤特异性膜蛋白,这些蛋白在癌细胞的细胞外表面构成异常表位。总之,我们展示了TS-TEAs和非典型膜蛋白在泛癌中的高流行率,它们可能具有潜在的治疗开发和靶向价值。

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