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Updated: Jun 10, 2025

Quantitative Immunohistochemistry of the Cellular Microenvironment in Patient Glioblastoma Resections
Published on: July 31, 2017
Targeting epigenetic mechanisms of resistance to chemotherapy in gliomas
Panagiotis Skouras1, Mariam Markouli2, Ioanna Papadatou3
1Department of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, Athens 11527, Greece; 1st Department of Neurosurgery, Evangelismos Hospital, National and Kapodistrian University of Athens, Greece.
Abstract:
Glioma, an aggressive type of brain tumors of glial origin is highly heterogeneous, posing significant treatment challenges due to its intrinsic resistance to conventional therapeutic schemes. It is characterized by an interplay between epigenetic and genetic alterations in key signaling pathways which further endorse their resistance potential. Aberrant DNA methylation patterns, histone modifications and non-coding RNAs may alter the expression of genes associated with drug response and cell survival, induce gene silencing or deregulate key pathways contributing to glioma resistance. There is evidence that epigenetic plasticity enables glioma cells to adapt dynamically to therapeutic schemes and allow the formation of drug-resistant subpopulations. Furthermore, the tumor microenvironment adds an extra input on epigenetic regulation, increasing the complexity of resistance mechanisms. Herein, we discuss epigenetic changes conferring to drug resistance mechanisms in gliomas in order to delineate novel therapeutic targets and potential approaches that will enable personalized treatment.
Insights
Glioma drug resistance stems from epigenetic changes like DNA methylation and histone modifications. Understanding these mechanisms can reveal new targets for personalized glioma treatments.
Area of Science:
- Neuro-oncology
- Epigenetics
- Cancer Biology
Background:
- Gliomas are aggressive brain tumors with significant treatment challenges.
- Tumor heterogeneity and intrinsic resistance limit conventional therapies.
- Epigenetic alterations interplay with genetic changes, enhancing glioma resistance.
Purpose of the Study:
- To discuss epigenetic changes contributing to drug resistance in gliomas.
- To identify novel therapeutic targets for overcoming glioma resistance.
- To explore potential approaches for personalized glioma treatment.
Main Methods:
- Review of current literature on glioma epigenetics and drug resistance.
- Analysis of epigenetic mechanisms including DNA methylation, histone modifications, and non-coding RNAs.
- Discussion of the role of epigenetic plasticity and the tumor microenvironment.
Main Results:
- Aberrant epigenetic patterns alter gene expression related to drug response and survival.
- Epigenetic plasticity allows glioma cells to adapt and form resistant subpopulations.
- The tumor microenvironment influences epigenetic regulation, complicating resistance.
Conclusions:
- Epigenetic modifications are key drivers of glioma drug resistance.
- Targeting epigenetic mechanisms offers potential for novel therapeutic strategies.
- Personalized treatment approaches informed by epigenetic insights are crucial for improving glioma outcomes.
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