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Updated: Aug 12, 2026

Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer
Published on: April 13, 2015
Telomerase as a universal tumor-associated antigen for cancer immunotherapy
1Department of Adult Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, MA 02115, USA.
Abstract:
Although the search for pharmacologic inhibitors of telomerase activity represents a promising approach for telomerase-based anti-cancer therapy, the immunological properties of the telomerase reverse transcriptase hTERT suggest that the enzyme is also an attractive target for novel immunotherapies against cancer. Data from both human and murine systems demonstrate that cytotoxic T-lymphocytes (CTL) can recognize peptides derived from TERT and kill TERT-positive tumor cells of multiple histologies. Given the vast overexpression of hTERT in human tumors and its low-level expression in rare normal tissues, clinical trials have begun that test the credentials of hTERT as a broadly applicable target for immunotherapy of cancer.
Insights
The human telomerase reverse transcriptase (hTERT) is a promising target for cancer immunotherapy. Cytotoxic T-lymphocytes recognize hTERT peptides, killing cancer cells, leading to clinical trials for hTERT-based cancer treatments.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Telomerase activity is crucial for cancer cell proliferation.
- Pharmacologic inhibition of telomerase is a known anti-cancer strategy.
- The human telomerase reverse transcriptase (hTERT) has unique immunological properties.
Purpose of the Study:
- To investigate the potential of hTERT as a target for cancer immunotherapy.
- To evaluate the immunogenicity of hTERT-derived peptides.
- To assess the efficacy of TERT-specific cytotoxic T-lymphocytes (CTL) in targeting cancer cells.
Main Methods:
- Analysis of TERT peptide recognition by human and murine cytotoxic T-lymphocytes (CTL).
- Assessment of CTL-mediated killing of TERT-positive tumor cells across various histologies.
- Evaluation of hTERT expression levels in tumor tissues versus normal tissues.
Main Results:
- Cytotoxic T-lymphocytes (CTL) can recognize peptides derived from TERT.
- TERT-specific CTLs effectively kill TERT-positive tumor cells.
- hTERT is overexpressed in most human tumors but minimally expressed in normal tissues.
Conclusions:
- hTERT is a viable and broadly applicable target for cancer immunotherapy.
- The immunogenicity of hTERT supports its use in novel anti-cancer therapies.
- Clinical trials are underway to validate hTERT-based immunotherapies for cancer treatment.
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