Related Experiment Video
Updated: Aug 30, 2026

Analysis of Human T Cell Activity in an Allogeneic Co-Culture Setting of Pre-Treated Tumor Cells
Published on: March 7, 2025
Epigenetic targets for immune intervention in human malignancies
Michele Maio1, Sandra Coral, Elisabetta Fratta
1Cancer Bioimmunotherapy Unit, Department of Medical Oncology, Centro di Riferimento Oncologico, Istituto di Ricovero e Cura a Carattere Scientifico, Aviano 33081, Italy. mmaio@cro.it
Abstract:
Emerging evidences suggest that epigenetic events associated with tumor development and progression, such as deregulated methylation of CpG dinucleotides and aberrant histone acetylation, may impair the immunogenic potential of cancer cells. In fact, DNA hypermethylation and/or histone deacetylation contribute to the absent or downregulated expression of different components of the 'tumor recognition complex' (i.e., HLA class I antigens, cancer/testis antigens and accessory/costimulatory molecules) in solid and hemopoietic human malignancies. However, pharmacologic agents that induce DNA hypomethylation or inhibit histone deacetylation can modify these epigenetic phenomena, restoring the defective expression of selected components of the 'tumor recognition complex' in cancer cells. These antigenic modifications positively modulate the immunogenicity and the immune recognition of cancer cells, making epigenetic drugs attractive agents to design new combined chemoimmunotherapeutic strategies for the treatment of cancer patients.
Insights
Epigenetic changes in cancer can suppress immune recognition. Epigenetic drugs can restore this recognition, offering new avenues for combined cancer therapy.
Area of Science:
- Oncology
- Immunology
- Epigenetics
Background:
- Epigenetic alterations, including DNA methylation and histone acetylation, are implicated in cancer development.
- These epigenetic changes can reduce the cancer cells' ability to be recognized by the immune system.
Purpose of the Study:
- To explore how epigenetic modifications affect cancer cell immunogenicity.
- To investigate the potential of epigenetic drugs in restoring anti-tumor immunity.
Main Methods:
- Review of emerging evidence on epigenetic events in cancer.
- Analysis of the impact of DNA methylation and histone deacetylation on tumor recognition complex components.
- Evaluation of pharmacologic agents targeting epigenetic modifications.
Main Results:
- Deregulated DNA methylation and histone acetylation impair cancer cell immunogenicity by downregulating key components of the tumor recognition complex.
- Pharmacologic agents that modify DNA methylation and histone acetylation can restore the expression of these components.
- Restored expression enhances cancer cell immunogenicity and immune recognition.
Conclusions:
- Epigenetic drugs can reverse immunosuppressive epigenetic changes in cancer cells.
- These drugs hold promise for developing novel chemoimmunotherapeutic strategies against cancer.
Related Concept Videos
Epigenetic Regulation
X-chromosome...
Epigenetic Regulation
Tumor Immunotherapy
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
The Tumor Microenvironment
Cytotoxic T Cells-mediated Immune Response
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
