Genomics Inform.  2019 Sep;17(3):e23. 10.5808/GI.2019.17.3.e23.

Identification of neoantigens derived from alternative splicing and RNA modification

Affiliations
  • 1Precision Medicine Research Center, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea. yejun@catholic.ac.kr
  • 2Integrated Research Center for Genome Polymorphism, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
  • 3Departments of Microbiology, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.

Abstract

The acquisition of somatic mutations is the most common event in cancer. Neoantigens expressed from genes with mutations acquired during carcinogenesis can be tumor-specific. Since the immune system recognizes tumor-specific peptides, they are potential targets for personalized neoantigen-based immunotherapy. However, the discovery of druggable neoantigens remains challenging, suggesting that a deeper understanding of the mechanism of neoantigen generation and better strategies to identify them will be required to realize the promise of neoantigen-based immunotherapy. Alternative splicing and RNA editing events are emerging mechanisms leading to neoantigen production. In this review, we outline recent work involving the large-scale screening of neoantigens produced by alternative splicing and RNA editing. We also describe strategies to predict and validate neoantigens from RNA sequencing data.

Keyword

alternative splicing; neoantigen; RNA editing

MeSH Terms

Alternative Splicing*
Carcinogenesis
Humans
Immune System
Immunotherapy
Mass Screening
Peptides
RNA Editing
RNA*
Sequence Analysis, RNA
Peptides
RNA
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