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Updated: Aug 15, 2026

Generation and Genetic Manipulation of Human Cervical Organoids
Published on: March 10, 2026
Epigenetics of cervical cancer. An overview and therapeutic perspectives
Alfonso Dueñas-González1, Marcela Lizano, Myrna Candelaria
1Unidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología/Instituto de Investigaciones Biomédicas (INCan/IIB), Universidad Nacional Autónoma de Mexico, Mexico City, Mexico. alfonso_duenasg@yahoo.com
Abstract:
Cervical cancer remains one of the greatest killers of women worldwide. It is difficult to foresee a dramatic increase in cure rate even with the most optimal combination of cytotoxic drugs, surgery, and radiation; therefore, testing of molecular targeted therapies against this malignancy is highly desirable. A number of epigenetic alterations occur during all stages of cervical carcinogenesis in both human papillomavirus and host cellular genomes, which include global DNA hypomethylation, hypermetylation of key tumor suppressor genes, and histone modifications. The reversible nature of epigenetic changes constitutes a target for transcriptional therapies, namely DNA methylation and histone deacetylase inhibitors. To date, studies in patients with cervical cancer have demonstrated the feasibility of reactivating the expression of hypermethylated and silenced tumor suppressor genes as well as the hyperacetylating and inhibitory effect upon histone deacetylase activity in tumor tissues after treatment with demethylating and histone deacetylase inhibitors. In addition, detection of epigenetic changes in cytological smears, serum DNA, and peripheral blood are of potential interest for development of novel biomolecular markers for early detection, prediction of response, and prognosis.
Insights
Epigenetic alterations in cervical cancer, such as DNA methylation changes, are reversible. Targeting these epigenetic modifications with inhibitors offers a promising therapeutic strategy for cervical cancer treatment and early detection.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Cervical cancer is a leading cause of cancer death in women globally.
- Current treatments (chemotherapy, surgery, radiation) have limitations in improving cure rates.
- Epigenetic alterations, including DNA hypomethylation and hypermethylation of tumor suppressor genes, are crucial in cervical carcinogenesis.
Purpose of the Study:
- To explore the potential of molecular targeted therapies for cervical cancer.
- To investigate epigenetic modifications as therapeutic targets.
- To assess the feasibility of using epigenetic changes as biomarkers for early detection and prognosis.
Main Methods:
- Review of studies on epigenetic alterations in cervical cancer.
- Analysis of the effects of DNA methylation and histone deacetylase inhibitors.
- Investigation of epigenetic markers in cytological smears, serum DNA, and peripheral blood.
Main Results:
- Epigenetic changes are present throughout cervical carcinogenesis.
- DNA methylation and histone deacetylase inhibitors can reactivate silenced tumor suppressor genes.
- These inhibitors demonstrate hyperacetylating and inhibitory effects on histone deacetylase activity in tumor tissues.
Conclusions:
- Epigenetic modifications represent a viable target for novel cervical cancer therapies.
- Demethylating and histone deacetylase inhibitors show promise in reactivating tumor suppressor genes.
- Epigenetic markers in various samples hold potential for early detection, treatment response prediction, and prognosis.
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