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Table 1 Advantages and disadvantages of current miRNA inhibitors and enhancer

From: Targeting miRNA by CRISPR/Cas in cancer: advantages and challenges

Methods

Type

Description

Examples

Target/function

Advantages

Limitations

miRNA mimics

Enhancer

miRNA mimic is chemically synthesized ds miRNA like RNA, designed to perform similar functions as endogenous miRNA

Let-7 mimic

MRX34 (a miRNA-34a mimic)

Delivery of let-7 mimic decreased the prevalence of K-ras-dependent lung cancers [57]

miRNA-34a mimics reduced tumor growth in liver cancer [58]

Predicted to target the same sets of genes because they share the same sequence as natural miRNA [59]

Have immune related adverse effects [60]

Causes non-specific changes of gene expression due to higher concentration delivery of mimics inside the cells [61]

Often chemically modified for stability which might have different effects than endogenous miRNA [61]

Might have negative effects because miRNA mimic complimentary strand acts inappropriately [62]

AntagomiRs

Inhibitor

AntagomiR is chemically synthesized single-stranded RNA and specially developed for inhibiting the function of endogenous miRNA

miR-10b antagomir

miR-10b antagomir reduced target protein, homeobox D10, and lung metastasis of breast cancer [63]

Chemical modification gives them higher affinity to cell membrane and higher stability [64]

Found to cause lowering of white blood cells, increase serum levels of bilirubin, ALT and AST [63]

miRNA sponges

Inhibitor

Contains complementary binding sites for target miRNA but produced within the cell by transgene

CDR1as/ciRS-7-lncRNA ZFAS1

Targets miRNA-7 mediated insulin secretion by islet cells [65]

Regulates miR-190a-3p to control the development of cervical cancer [66]

Easy to deliver into difficult-to-transfect cell lines or cells in vivo by viral vector [67]

Sponges interact with the mature miRNA, thus clustering of miRNA precursors does not affect their effectiveness [67]

Binds in the seeding region of the miRNA, thus might inhibit many genes by targeting many miRNAs of the same family [67]

LNA-modified antisense oligonucleotides

Inhibitor

RNA analogs in which a methylene connection between the 2′-oxygen and the 4′-carbon “locks” the ribose ring

miR-92a-3p

Inhibits miR-92a-3p induced colon cancer cells proliferation [68]

Regulates EMT to prevent miR-205-5p-mediated breast cancer metastasis [69]

Chemical modification gives them more affinity to the target and stability towards endogenous nucleases activity [70]

They would increase nuclease resistance and prevent the targeted probe from degradation; they cannot be inserted at the 5′ terminus of the probe or at the nearby nucleotide [71]

  1. MRX34 liposomal formulation of miR-34a, ALT alanine transaminase, AST aspartate aminotransferase, CDR1 cerebellar degeneration-related protein 1, LNA locked nucleic acid, EMT epithelial-mesenchymal transition