2019
DOI: 10.1002/jcb.29364
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RNA therapeutics: Identification of novel targets leading to drug discovery

Abstract: The established concept that RNA works only for protein synthesis has been changed over the past few decades and shifted towards therapeutic purposes. Almost 98% of mammalian genome is transcribed into nonprotein coding RNA termed as noncoding RNA (ncRNA) which plays regulatory role in molecular and cellular functions as controlling gene expression. These ncRNAs are classified as long noncoding RNA (lncRNA), short noncoding RNA (sncRNA), and translational/structural RNA which possess diverse functions. These n… Show more

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Cited by 36 publications
(17 citation statements)
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References 253 publications
(489 reference statements)
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“…In China, ncRNAs have been used for cancer diagnosis in the form of diagnostic kits. Qadir et al (87) attempted to summarize the emerging field of ncRNAs and their role in different diseases, including cancer, their modes of action, and their potential in target identification and therapeutic drug development. In addition, some gene editing techniques have been used for cancer treatment, such as CRISPR.…”
Section: Lncrnas and Mirnas In Cancermentioning
confidence: 99%
“…In China, ncRNAs have been used for cancer diagnosis in the form of diagnostic kits. Qadir et al (87) attempted to summarize the emerging field of ncRNAs and their role in different diseases, including cancer, their modes of action, and their potential in target identification and therapeutic drug development. In addition, some gene editing techniques have been used for cancer treatment, such as CRISPR.…”
Section: Lncrnas and Mirnas In Cancermentioning
confidence: 99%
“…The therapeutic effects are achieved through the regulation of RNA maturation, splicing, interference, translation and stabilisation. More possibilities of drug formats and therapeutic mechanisms have been discussed, including peptides [182], aptamers [183] and RNA editing with CRISPR-Cas13 [184]. Over the past five years, an increasing number of RNA-targeted drugs have been approved.…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%
“…This realization of this concept is possible due to significant developments in genetic engineering. For example, the targeted genetic deletion of Malat1 by zinc finger nucleases 57 and synthetic oligonucleotides designed to Malat1 as a therapeutic target, including siRNAs and locked nucleic acid (LNA) gapmer antisense oligonucleotides (ASOs), [58][59][60] are worthy of consideration.…”
Section: Modulating the Disease Processmentioning
confidence: 99%