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Small molecules targeting microRNA for cancer therapy: Promises and obstacles.

作者信息

Wen Di, Danquah Michael, Chaudhary Amit Kumar, Mahato Ram I

机构信息

Department of Pharmaceutical Sciences, University of Nebraska Medical Center, 986025 Nebraska Medical Center, Omaha, NE 68198-6025, USA.

Department of Pharmaceutical Sciences, Chicago State University, 9501 South King Drive., Chicago, IL 60628, USA.

出版信息

J Control Release. 2015 Dec 10;219:237-247. doi: 10.1016/j.jconrel.2015.08.011. Epub 2015 Aug 6.


DOI:10.1016/j.jconrel.2015.08.011
PMID:26256260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4749151/
Abstract

Aberrant expression of miRNAs is critically implicated in cancer initiation and progression. Therapeutic approaches focused on regulating miRNAs are therefore a promising approach for treating cancer. Antisense oligonucleotides, miRNA sponges, and CRISPR/Cas9 genome editing systems are being investigated as tools for regulating miRNAs. Despite the accruing insights in the use of these tools, delivery concerns have mitigated clinical application of such systems. In contrast, little attention has been given to the potential of small molecules to modulate miRNA expression for cancer therapy. In these years, many researches proved that small molecules targeting cancer-related miRNAs might have greater potential for cancer treatment. Small molecules targeting cancer related miRNAs showed significantly promising results in different cancer models. However, there are still several obstacles hindering the progress and clinical application in this area. This review discusses the development, mechanisms and application of small molecules for modulating oncogenic miRNAs (oncomiRs). Attention has also been given to screening technologies and perspectives aimed to facilitate clinical translation for small molecule-based miRNA therapeutics.

摘要

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本文引用的文献

[1]
Single-Vehicular Delivery of Antagomir and Small Molecules to Inhibit miR-122 Function in Hepatocellular Carcinoma Cells by using "Smart" Mesoporous Silica Nanoparticles.

Angew Chem Int Ed Engl. 2015-7-15

[2]
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Oncotarget. 2015-6-30

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Oncol Rep. 2015-6

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Biomed Pharmacother. 2015-4

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Mol Cell Biochem. 2015-7

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Int J Mol Med. 2015-5

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