Targeting a shared neoepitope derived from non-canonical translation of c-MYConcogene in cancer cells

Abstract

AbstractCancer cells rely on alternative modes of translation for protein synthesis, promoting internal ribosome entry site (IRES)-dependent translation of mRNA encoding pro-oncogenic factors. Furthermore, ribosomes translate mRNA with lower fidelity in tumor cells. We proposed that these translational modifications in cancer produce shared tumor-specific epitopes derived from IRES-containing oncogenes. To identify such neoepitopes, we developed anin silico-based method that we applied toc-MYC. We showed that the non-canonical translation ofc-MYCmRNA in cancer cells, involving a (+1) ribosomal frameshift, generates a shared neoepitope which induces high-avidity T cells able to kill tumor cellsin vitroandin vivowhile sparing normal cells. Our data provide preclinical rationale for developing immunotherapies targeting thisc-MYC-derived neoepitope and validate a new type of shared translation-associated neoantigens.