» Articles » PMID: 36604431

Neoantigens: Promising Targets for Cancer Therapy

Overview
Date 2023 Jan 5
PMID 36604431
Authors
Affiliations
Soon will be listed here.
Abstract

Recent advances in neoantigen research have accelerated the development and regulatory approval of tumor immunotherapies, including cancer vaccines, adoptive cell therapy and antibody-based therapies, especially for solid tumors. Neoantigens are newly formed antigens generated by tumor cells as a result of various tumor-specific alterations, such as genomic mutation, dysregulated RNA splicing, disordered post-translational modification, and integrated viral open reading frames. Neoantigens are recognized as non-self and trigger an immune response that is not subject to central and peripheral tolerance. The quick identification and prediction of tumor-specific neoantigens have been made possible by the advanced development of next-generation sequencing and bioinformatic technologies. Compared to tumor-associated antigens, the highly immunogenic and tumor-specific neoantigens provide emerging targets for personalized cancer immunotherapies, and serve as prospective predictors for tumor survival prognosis and immune checkpoint blockade responses. The development of cancer therapies will be aided by understanding the mechanism underlying neoantigen-induced anti-tumor immune response and by streamlining the process of neoantigen-based immunotherapies. This review provides an overview on the identification and characterization of neoantigens and outlines the clinical applications of prospective immunotherapeutic strategies based on neoantigens. We also explore their current status, inherent challenges, and clinical translation potential.

Citing Articles

Neoantigen-based mRNA vaccine exhibits superior anti-tumor activity compared to synthetic long peptides in an in vivo lung carcinoma model.

Nguyen C, Vu T, Nguyen M, Tran-Nguyen T, Huynh C, Ha Q Cancer Immunol Immunother. 2025; 74(4):145.

PMID: 40072566 DOI: 10.1007/s00262-025-03992-7.


Computational modeling of human genetic variants in mice.

Dong K, Gould S, Li M, Sanchez Rivera F bioRxiv. 2025; .

PMID: 40060429 PMC: 11888284. DOI: 10.1101/2025.02.23.639784.


Integration of proteomics profiling data to facilitate discovery of cancer neoantigens: a survey.

Luo S, Peng H, Shi Y, Cai J, Zhang S, Shao N Brief Bioinform. 2025; 26(2).

PMID: 40052441 PMC: 11886573. DOI: 10.1093/bib/bbaf087.


The immunopeptidome of colon cancer cells treated with topoisomerase inhibiting drug reveals differential as well as common endogenous protein sampling and display of MHC I-associated peptides.

Bedi D, Hassan M, Yirsaw A, Vikas B, Datta P, Samuel T Mol Cell Oncol. 2025; 12(1):2471640.

PMID: 40051755 PMC: 11881837. DOI: 10.1080/23723556.2025.2471640.


Enhancing immunotherapy with tumour-responsive nanomaterials.

Linderman S, DeRidder L, Sanjurjo L, Foote M, Alonso M, Kirtane A Nat Rev Clin Oncol. 2025; .

PMID: 40050505 DOI: 10.1038/s41571-025-01000-6.


References
1.
Zheng S, Asnani M, Thomas-Tikhonenko A . Escape From ALL-CARTaz: Leukemia Immunoediting in the Age of Chimeric Antigen Receptors. Cancer J. 2019; 25(3):217-222. PMC: 6617517. DOI: 10.1097/PPO.0000000000000381. View

2.
Sahin U, Oehm P, Derhovanessian E, Jabulowsky R, Vormehr M, Gold M . An RNA vaccine drives immunity in checkpoint-inhibitor-treated melanoma. Nature. 2020; 585(7823):107-112. DOI: 10.1038/s41586-020-2537-9. View

3.
Celik A, Kervestin S, Jacobson A . NMD: At the crossroads between translation termination and ribosome recycling. Biochimie. 2014; 114:2-9. PMC: 4430455. DOI: 10.1016/j.biochi.2014.10.027. View

4.
McLaughlin M, Patin E, Pedersen M, Wilkins A, Dillon M, Melcher A . Inflammatory microenvironment remodelling by tumour cells after radiotherapy. Nat Rev Cancer. 2020; 20(4):203-217. DOI: 10.1038/s41568-020-0246-1. View

5.
Dorrie J, Schaft N, Schuler G, Schuler-Thurner B . Therapeutic Cancer Vaccination with Ex Vivo RNA-Transfected Dendritic Cells-An Update. Pharmaceutics. 2020; 12(2). PMC: 7076681. DOI: 10.3390/pharmaceutics12020092. View