- Author:
	        		
		        		
		        		
			        		Jiyeon PARK
			        		
			        		
			        		
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			        		Yeun Jun CHUNG
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Review
 - Keywords: alternative splicing; neoantigen; RNA editing
 - MeSH: Alternative Splicing; Carcinogenesis; Humans; Immune System; Immunotherapy; Mass Screening; Peptides; RNA Editing; RNA; Sequence Analysis, RNA
 - From:Genomics & Informatics 2019;17(3):e23-
 - CountryRepublic of Korea
 - Language:English
 - 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.
 
            
