Target intelligence / Profile preview

Cancer cell neoantigen

Molecular classification
Other (Neoantigens are not a single protein or gene family, but a class of mutated antigens unique to cancer cells)
01

Overview

Cancer cell neoantigens are novel protein antigens that arise from mutations in the DNA of tumor cells. These mutations—such as point mutations, insertions, deletions, alternative splicing events, or gene rearrangements—alter the amino acid sequence of proteins produced by cancer cells. The resulting mutant proteins are processed into peptides that are presented on the surface of cancer cells via human leukocyte antigen (HLA) molecules. Because these altered peptides do not exist in normal tissues and are recognized as "non-self" by the immune system, they can stimulate strong anti-tumor T-cell responses. There are two main types: shared neoantigens (arising from common driver mutations across patients) and personalized/unique neoantigens (specific to an individual’s tumor). Neoantigen-based therapies—including personalized vaccines—are being developed to harness this specificity for targeted immunotherapy against cancers while minimizing damage to healthy tissue.

Other names
NeoantigenTumor neoantigenCancer neoantigenNeoplasm antigen
02

Mechanism of action

Induction of anti-tumor T-cell responses by presenting mutated peptides on HLA molecules, leading to recognition and destruction of tumor cells by the immune system

03

Biological functions

Immune response (stimulate anti-tumor T-cell responses)Tumor immune evasion (can be involved in mechanisms by which tumors escape immune detection)
04

Disease associations

Cancer
05

Safety considerations

Tumor heterogeneity may limit effectiveness due to variability in neoantigen expression between patients or within tumorsPotential for immune-related adverse events if off-target effects occur, though risk is generally lower than with non-mutated self-antigens
06

Interacting drugs

Personalized cancer vaccines targeting specific neoantigens
07

Biomarkers

Presence and profile of tumor-specific neoantigens can serve as biomarkers for immunotherapy selection and monitoring efficacy

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