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Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma

BACKGROUND: Oligonucleotide drug development has revolutionised the drug discovery field. Within this field, ‘small’ or ‘short’ activating RNAs (saRNA) are a more recently discovered category of short double-stranded RNA with clinical potential. saRNAs promote transcription from target loci, a pheno...

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Autores principales: Setten, Ryan L., Lightfoot, Helen L., Habib, Nagy A., Rossi, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204661/
https://www.ncbi.nlm.nih.gov/pubmed/29886828
http://dx.doi.org/10.2174/1389201019666180611093428
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author Setten, Ryan L.
Lightfoot, Helen L.
Habib, Nagy A.
Rossi, John J.
author_facet Setten, Ryan L.
Lightfoot, Helen L.
Habib, Nagy A.
Rossi, John J.
author_sort Setten, Ryan L.
collection PubMed
description BACKGROUND: Oligonucleotide drug development has revolutionised the drug discovery field. Within this field, ‘small’ or ‘short’ activating RNAs (saRNA) are a more recently discovered category of short double-stranded RNA with clinical potential. saRNAs promote transcription from target loci, a phenomenon widely observed in mammals known as RNA activation (RNAa). OBJECTIVE: The ability to target a particular gene is dependent on the sequence of the saRNA. Hence, the potential clinical application of saRNAs is to increase target gene expression in a sequence-specific man-ner. saRNA-based therapeutics present opportunities for expanding the “druggable genome” with partic-ular areas of interest including transcription factor activation and cases of haploinsufficiency. Results and CONCLUSION: In this mini-review, we describe the pre-clinical development of the first saRNA drug to enter the clinic. This saRNA, referred to as MTL-CEBPA, induces increased expression of the transcription factor CCAAT/enhancer-binding protein alpha (CEBPα), a tumour suppressor and critical regulator of hepatocyte function. MTL-CEBPA is presently in Phase I clinical trials for hepatocel-lular carcinoma (HCC). The clinical development of MTL-CEBPA will demonstrate “proof of concept” that saRNAs can provide the basis for drugs which enhance target gene expression and consequently improve treatment outcome in patients
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spelling pubmed-62046612018-11-16 Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma Setten, Ryan L. Lightfoot, Helen L. Habib, Nagy A. Rossi, John J. Curr Pharm Biotechnol Article BACKGROUND: Oligonucleotide drug development has revolutionised the drug discovery field. Within this field, ‘small’ or ‘short’ activating RNAs (saRNA) are a more recently discovered category of short double-stranded RNA with clinical potential. saRNAs promote transcription from target loci, a phenomenon widely observed in mammals known as RNA activation (RNAa). OBJECTIVE: The ability to target a particular gene is dependent on the sequence of the saRNA. Hence, the potential clinical application of saRNAs is to increase target gene expression in a sequence-specific man-ner. saRNA-based therapeutics present opportunities for expanding the “druggable genome” with partic-ular areas of interest including transcription factor activation and cases of haploinsufficiency. Results and CONCLUSION: In this mini-review, we describe the pre-clinical development of the first saRNA drug to enter the clinic. This saRNA, referred to as MTL-CEBPA, induces increased expression of the transcription factor CCAAT/enhancer-binding protein alpha (CEBPα), a tumour suppressor and critical regulator of hepatocyte function. MTL-CEBPA is presently in Phase I clinical trials for hepatocel-lular carcinoma (HCC). The clinical development of MTL-CEBPA will demonstrate “proof of concept” that saRNAs can provide the basis for drugs which enhance target gene expression and consequently improve treatment outcome in patients Bentham Science Publishers 2018-07 2018-07 /pmc/articles/PMC6204661/ /pubmed/29886828 http://dx.doi.org/10.2174/1389201019666180611093428 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Setten, Ryan L.
Lightfoot, Helen L.
Habib, Nagy A.
Rossi, John J.
Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma
title Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma
title_full Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma
title_fullStr Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma
title_full_unstemmed Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma
title_short Development of MTL-CEBPA: Small Activating RNA Drug for Hepatocellular Carcinoma
title_sort development of mtl-cebpa: small activating rna drug for hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204661/
https://www.ncbi.nlm.nih.gov/pubmed/29886828
http://dx.doi.org/10.2174/1389201019666180611093428
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