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.

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.