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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2018
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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 |
format | Online Article Text |
id | pubmed-6204661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
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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