Related Experiment Video
Updated: Jan 31, 2026

Measuring Growth and Gene Expression Dynamics of Tumor-Targeted S. Typhimurium Bacteria
Published on: July 6, 2013
Cancer immunotherapy targeting neoantigens derived from tumor-specific gene mutations
Abstract:
Cancer immunotherapies targeting "tumor-associated antigens" derived from wild-type proteins have shown limited success in clinical trials to date. Recent development of next generation sequencing and bioinformatics technology has allowed identification of "neoanti- gens" derived from genetic alterations, such as mutations, insertions, and deletions, re- stricted to tumor cells. Tumor-specific neoantigens, but not tumor-associated antigens, can be recognized as "foreign" by the host immune system. Therefore, they might show higher immunogenicity and more efficiently activate anti-tumor immune responses capable of con- trolling tumor burden. In this review article, I have summarized and discussed clinical signifi- cance of tumor-specific neoantigens and their potential clinical application for personalized cancer immunotherapies.
Insights
Tumor-specific neoantigens, unlike tumor-associated antigens, are recognized as foreign by the immune system. This recognition may lead to more effective personalized cancer immunotherapies by activating stronger anti-tumor responses.
Area of Science:
- Oncology
- Immunology
- Bioinformatics
Background:
- Cancer immunotherapies targeting tumor-associated antigens (TAAs) have yielded limited clinical success.
- TAAs are derived from wild-type proteins and are not always tumor-specific.
Purpose of the Study:
- To review the clinical significance of tumor-specific neoantigens (TSNAs).
- To discuss the potential of TSNAs in personalized cancer immunotherapy.
Main Methods:
- Review of recent advancements in next-generation sequencing and bioinformatics.
- Analysis of literature on neoantigens derived from tumor-specific genetic alterations (mutations, insertions, deletions).
Main Results:
- Tumor-specific neoantigens are recognized as foreign by the host immune system, unlike TAAs.
- TSNAs exhibit higher immunogenicity, potentially leading to more effective anti-tumor immune responses.
Conclusions:
- TSNAs hold significant promise for developing personalized cancer immunotherapies.
- Targeting TSNAs may offer a more effective strategy for controlling tumor burden compared to TAAs.
Related Concept Videos
Tumor Immunotherapy
Mutation, Gene Flow, and Genetic Drift
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Cell Specific Gene Expression
Mutations
Targeted Cancer Therapies
There are several types of targeted therapies against...

