Exploiting microRNAs As Cancer Therapeutics

被引:0
作者
Tamsin Robb
Glen Reid
Cherie Blenkiron
机构
[1] The University of Auckland,Department of Molecular Medicine and Pathology
[2] Asbestos Diseases Research Institute (ADRI),Sydney Medical School
[3] The University of Sydney,School of Biological Sciences
[4] The University of Auckland,undefined
[5] The University of Auckland,undefined
来源
Targeted Oncology | 2017年 / 12卷
关键词
Chronic Lymphocytic Leukaemia; miRNA Expression; Malignant Pleural Mesothelioma; Lock Nucleic Acid; Cancer Therapeutics;
D O I
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中图分类号
学科分类号
摘要
miRNAs are a well-studied class of non-coding RNAs, predominantly functioning to down-regulate gene expression from messenger RNA (mRNA) in a targeted manner by binding to complementary sequence on the target mRNA. Many miRNAs have been linked to the development of hallmarks of cancer. miRNAs represent valuable therapeutic targets to exploit in the search for novel cancer treatments, due to their ubiquitous expression and their ability to tightly regulate the gene expression of a whole host of genes and pathways in a single hit. The miRNA system may be harnessed for therapeutic use either through replacement of tumour suppressive miRNAs lost in cancer, or through inhibition of oncogenic miRNAs overexpressed in cancer. There is a large body of work investigating optimal systemic and localised delivery strategies, and while miRNA therapeutics show promise, it is clear that further developments to delivery strategies may be required to allow safe translation of miRNAs to the clinic. The information gleaned from miRNA signatures as biomarkers is already proving invaluable in the fight to better understand and treat individual tumours, and there is great promise to the applications of these small, but mighty molecules in the future of cancer therapeutics.[graphic not available: see fulltext]
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页码:163 / 178
页数:15
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