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Published on: October 4, 2019
The Role of MicroRNAs in Therapeutic Resistance of Malignant Primary Brain Tumors
Ilgiz Gareev1, Ozal Beylerli1, Yanchao Liang2,3
1Central Research Laboratory, Bashkir State Medical University, Ufa, Russia.
Abstract:
Brain tumors in children and adults are challenging tumors to treat. Malignant primary brain tumors (MPBTs) such as glioblastoma have very poor outcomes, emphasizing the need to better understand their pathogenesis. Developing novel strategies to slow down or even stop the growth of brain tumors remains one of the major clinical challenges. Modern treatment strategies for MPBTs are based on open surgery, chemotherapy, and radiation therapy. However, none of these treatments, alone or in combination, are considered effective in controlling tumor progression. MicroRNAs (miRNAs) are 18-22 nucleotide long endogenous non-coding RNAs that regulate gene expression at the post-transcriptional level by interacting with 3'-untranslated regions (3'-UTR) of mRNA-targets. It has been proven that miRNAs play a significant role in various biological processes, including the cell cycle, apoptosis, proliferation, differentiation, etc. Over the last decade, there has been an emergence of a large number of studies devoted to the role of miRNAs in the oncogenesis of brain tumors and the development of resistance to radio- and chemotherapy. Wherein, among the variety of molecules secreted by tumor cells into the external environment, extracellular vesicles (EVs) (exosomes and microvesicles) play a special role. Various elements were found in the EVs, including miRNAs, which can be transported as part of these EVs both between neighboring cells and between remotely located cells of different tissues using biological fluids. Some of these miRNAs in EVs can contribute to the development of resistance to radio- and chemotherapy in MPBTs, including multidrug resistance (MDR). This comprehensive review examines the role of miRNAs in the resistance of MPBTs (e.g., high-grade meningiomas, medulloblastoma (MB), pituitary adenomas (PAs) with aggressive behavior, and glioblastoma) to chemoradiotherapy and pharmacological treatment. It is believed that miRNAs are future therapeutic targets in MPBTs and such the role of miRNAs needs to be critically evaluated to focus on solving the problems of resistance to therapy this kind of human tumors.
Insights
MicroRNAs (miRNAs) are key regulators in brain tumor development and treatment resistance. This review explores how miRNAs, often within extracellular vesicles, contribute to resistance against chemoradiotherapy in malignant primary brain tumors.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Malignant primary brain tumors (MPBTs) present significant treatment challenges with poor patient outcomes.
- Current treatments like surgery, chemotherapy, and radiation therapy are often ineffective in controlling tumor progression.
- MicroRNAs (miRNAs) are crucial regulators of gene expression involved in cellular processes like proliferation and apoptosis, and their role in oncogenesis and treatment resistance is increasingly recognized.
Purpose of the Study:
- To comprehensively review the role of miRNAs in the resistance of MPBTs to chemoradiotherapy and pharmacological treatments.
- To evaluate the function of miRNAs, particularly those encapsulated in extracellular vesicles (EVs), in mediating multidrug resistance (MDR) in brain tumors.
- To highlight miRNAs as potential future therapeutic targets for overcoming treatment resistance in MPBTs.
Main Methods:
- Literature review of studies investigating miRNA involvement in brain tumor pathogenesis and treatment resistance.
- Analysis of the role of extracellular vesicles (EVs) in transporting miRNAs between cells.
- Examination of specific MPBTs including glioblastoma, medulloblastoma (MB), high-grade meningiomas, and aggressive pituitary adenomas (PAs).
Main Results:
- miRNAs play a significant role in the oncogenesis of MPBTs and the development of resistance to radio- and chemotherapy.
- Extracellular vesicles (EVs) facilitate the intercellular transfer of miRNAs, contributing to treatment resistance, including multidrug resistance (MDR).
- Specific miRNAs within EVs can promote resistance to chemoradiotherapy and pharmacological agents in various MPBTs.
Conclusions:
- miRNAs are critical mediators of treatment resistance in malignant primary brain tumors.
- Targeting miRNAs, especially those transported via EVs, holds promise for novel therapeutic strategies against MPBTs.
- Further critical evaluation of miRNA roles is essential to develop effective therapies for overcoming resistance in brain tumors.
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