Bioinformatic methods for cancer neoantigen prediction

被引:26
作者
Boegel, Sebastian [1 ]
Castle, John C. [3 ]
Kodysh, Julia [2 ]
O'Donnell, Timothy [2 ]
Rubinsteyn, Alex [2 ]
机构
[1] Johannes Gutenberg Univ Mainz, Mainz, Germany
[2] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[3] Agenus Inc, Lexington, MA USA
来源
CANCER IMMUNOTHERAPY | 2019年 / 164卷
关键词
MHC CLASS-I; ALTERNATIVE SPLICING EVENTS; T-CELL EPITOPES; BINDING-AFFINITY; PEPTIDE-BINDING; WHOLE-GENOME; LUNG-CANCER; COPY NUMBER; HLA; TUMOR;
D O I
10.1016/bs.pmbts.2019.06.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor cells accumulate aberrations not present in normal cells, leading to presentation of neoantigens on MHC molecules on their surface. These non-self neoantigens distinguish tumor cells from normal cells to the immune system and are thus targets for cancer immunotherapy. The rapid development of molecular profiling platforms, such as next-generation sequencing, has enabled the generation of large datasets characterizing tumor cells. The simultaneous development of algorithms has enabled rapid and accurate processing of these data. Bioinformatic software tools encoding the algorithms can be strung together in a workflow to identify neoantigens. Here, with a focus on high-throughput sequencing, we review state-of-the art bioinformatic tools along with the steps and challenges involved in neoantigen identification and recognition.
引用
收藏
页码:25 / 60
页数:36
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