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Published on: October 4, 2019
Exosomal noncoding RNAs: key players in glioblastoma drug resistance
Ahmad Movahedpour1,2, Seyyed Hossein Khatami3, Marjan Khorsand4
1Department of Medical Biotechnology, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.
Abstract:
Glioma, as one of the most severe human malignancies, is defined as the Central Nervous System's (CNS) tumors. Glioblastoma (GBM) in this regard, is the most malignant type of gliomas. There are multiple therapeutic strategies to cure GBM, for which chemotherapy is often the first-line treatment. Still, various cellular processes, such as uncontrolled proliferation, invasion and metastasis, may disturb the treatment efficacy. Drug resistance is another process in this way, which can also cause undesirable effects. Thereupon, identifying the mechanisms, involved in developing drug resistance and the relevant mechanisms can be very helpful in GBM management. The discovery of exosomal non-coding RNAs (ncRNAs), RNA molecules that can be transferred between the cells and different tissues using the exosomes, was a milestone in this regard. It has been revealed that the key exosomal ncRNAs, including circular RNAs, microRNAs, and long ncRNAs, are able to modulate GBM drug resistance through different signaling pathways or by affecting regulatory proteins and their corresponding genes. Nowadays, researchers are trying to overcome the limitations of chemotherapy by targeting these RNA molecules. Accordingly, this review aims to clarify the substantial roles of exosomal ncRNAs in GBM drug resistance and involved mechanisms.
Insights
Exosomal non-coding RNAs (ncRNAs) play a key role in glioblastoma (GBM) chemotherapy resistance. Targeting these exosomal ncRNAs offers a promising strategy to overcome treatment limitations in GBM patients.
Area of Science:
- Neuro-oncology
- Molecular Biology
- Cancer Research
Background:
- Glioblastoma (GBM) is a highly aggressive Central Nervous System (CNS) tumor.
- Chemotherapy is a primary treatment for GBM, but its efficacy is often compromised by drug resistance.
- Understanding the mechanisms of drug resistance is crucial for effective GBM management.
Purpose of the Study:
- To elucidate the significant roles of exosomal non-coding RNAs (ncRNAs) in GBM drug resistance.
- To clarify the underlying mechanisms by which exosomal ncRNAs modulate GBM chemotherapy resistance.
- To highlight the potential of targeting exosomal ncRNAs as a therapeutic strategy for GBM.
Main Methods:
- Review of current literature on exosomal ncRNAs and GBM drug resistance.
- Analysis of signaling pathways and regulatory proteins affected by exosomal ncRNAs.
- Synthesis of information on the therapeutic targeting of exosomal ncRNAs in GBM.
Main Results:
- Exosomal ncRNAs, including circular RNAs, microRNAs, and long ncRNAs, are key mediators of GBM drug resistance.
- These ncRNAs influence GBM drug resistance by modulating signaling pathways and regulatory proteins.
- Exosomal ncRNAs can be transferred between cells, impacting the tumor microenvironment and treatment response.
Conclusions:
- Exosomal ncRNAs represent a critical mechanism driving GBM chemotherapy resistance.
- Targeting specific exosomal ncRNAs holds potential for novel therapeutic interventions in GBM.
- Further research into exosomal ncRNA mechanisms can lead to improved GBM treatment strategies.
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