Abstract

In the field of molecular oncology, microRNAs (miRNAs) and their role in regulating physiological processes and cancer pathogenesis have been a revolutionary discovery over the last decade. It is now considered that miRNA dysregulation influences critical molecular pathways involved in tumor progression, invasion, angiogenesis and metastasis in a wide range of cancer types. Hence, altering miRNA levels in cancer cells has promising potential as a therapeutic intervention, which is discussed in many other articles in this Special Issue. Some of the most significant hurdles in therapeutic miRNA usage are the stability and the delivery system. In this review, we cover a comprehensive update on the challenges and strategies for the development of therapeutic miRNA delivery systems that includes virus-based delivery, non-viral delivery (artificial lipid-based vesicles, polymer-based or chemical structures), and recently emerged extracellular vesicle (EV)-based delivery systems.

Highlights

  • UMR DIATHEC, EA 7294, Centre Européen d’Etude du Diabète, 67200 Strasbourg, France; Department of Cardiovascular Physiology, Tokyo Medical and Dental University, Tokyo 113-8510, Japan; Institute for Quantitative Health Sciences and Engineering (IQ), Michigan State University, East Lansing, MI 48824, USA

  • The development of strategies aimed to efficiently deliver miRNAs will enhance the effectiveness of therapeutic interventions

  • MiRNAs are one of the most promising therapeutic targets with well-characterized expressions and functions within cancer cells with high specificity to cancer-related pathways. Their delivery remains a challenge for miRNA therapeutics

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Summary

A Comprehensive Review of Cancer MicroRNA

UMR DIATHEC, EA 7294, Centre Européen d’Etude du Diabète, 67200 Strasbourg, France;. Institute for Quantitative Health Sciences and Engineering (IQ), Michigan State University, East Lansing, MI 48824, USA.

MicroRNA Overview
Altered miRNA Profile in Malignancies
MiRNA Editing as Cancer Therapy
MiRNA Inhibition Therapies for OncomiRs
MiRNA Replacement Therapies for Tumor-Suppressor MiRNAs
Local Delivery
Systemic Delivery
Viral Delivery
Non-Viral Delivery
Nanoparticles
Polymer-based Vectors
Inorganic Vectors
Other Biomaterials
Therapeutic MiRNA Candidates in Preclinical Studies
Clinical Studies Involving MiRNA-Based Therapy
Findings
Conclusions
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