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Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
Bioengineered chimeric tRNA/pre-miRNAs as prodrugs in cancer therapy
Fatemeh Rafieenia1, Seyed Omar Ebrahimi2, Ensieh Sadat Emadi2
1Department of Medical Genetics, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Abstract:
Today, biologic prodrugs have led to targeting specific tumor markers and have increased specificity and selectivity in cancer therapy. Various studies have shown the role of ncRNAs in cancer pathology and tumorigenesis and have suggested that ncRNAs, especially miRNAs, are valuable molecules in understanding cancer biology and therapeutic processes. Most miRNAs-based research and treatment are limited to chemically synthesized miRNAs. Synthetic alterations in these miRNA mimics may affect their folding, safety profile, and even biological activity. However, despite synthetic miRNA mimics produced by automated systems, various carriers could be used to achieve efficient production of bioengineered miRNAs through economical microbial fermentation. These bioengineered miRNAs as biological prodrugs could provide a new approach for safe therapeutic methods and drug production. In this regard, bioengineered chimeric miRNAs could be selectively processed to mature miRNAs in different types of cancer cells by targeting the desired gene and regulating cancer progression. In this article, we aim to review bioengineered miRNAs and their use in cancer therapy, as well as offering advances in this area, including the use of chimeric tRNA/pre-miRNAs.
Insights
Bioengineered microRNAs (miRNAs) offer a safer, more effective cancer therapy approach than synthetic versions. Microbial fermentation enables economical production of these biological prodrugs for targeted cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Non-coding RNAs (ncRNAs), particularly microRNAs (miRNAs), play crucial roles in cancer pathology and tumorigenesis.
- Current miRNA-based cancer therapies predominantly rely on chemically synthesized miRNAs, which can have limitations in safety and biological activity.
- Bioengineered miRNAs present an alternative to synthetic mimics, potentially overcoming issues related to folding, safety, and efficacy.
Purpose of the Study:
- To review the advancements in bioengineered microRNAs (miRNAs) for cancer therapy.
- To explore the potential of bioengineered miRNAs as biological prodrugs for targeted cancer treatment.
- To discuss novel approaches, including chimeric tRNA/pre-miRNAs, in the field of bioengineered miRNA therapeutics.
Main Methods:
- Utilizing microbial fermentation for the economical production of bioengineered miRNAs.
- Developing bioengineered chimeric miRNAs for selective processing in cancer cells.
- Investigating the use of various carriers for efficient delivery of bioengineered miRNAs.
Main Results:
- Bioengineered miRNAs produced via microbial fermentation offer a cost-effective and potentially safer alternative to synthetic miRNAs.
- Chimeric miRNAs can be engineered for targeted delivery and selective activation within cancer cells.
- This approach holds promise for developing novel, highly specific cancer therapeutics.
Conclusions:
- Bioengineered miRNAs represent a promising new avenue for cancer therapy, offering improved safety and specificity.
- Economical production through microbial fermentation makes this approach scalable and accessible.
- Further research into bioengineered chimeric miRNAs, including tRNA/pre-miRNA constructs, is warranted for advancing cancer treatment strategies.
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