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

Curr Pharm Biotechnol. 2018;19(8):611-621. doi: 10.2174/1389201019666180611093428.

Abstract

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 manner. saRNA-based therapeutics present opportunities for expanding the "druggable genome" with particular 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 hepatocellular 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.

Keywords: CEBPα; MTL-CEBPA; MiNA therapeutics; RNA therapeutics; hepatocellular carcinoma; liver; saRNA..

Publication types

  • Review

MeSH terms

  • Animals
  • CCAAT-Enhancer-Binding Proteins / administration & dosage
  • CCAAT-Enhancer-Binding Proteins / genetics*
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / genetics*
  • Gene Expression Regulation
  • Genes, Tumor Suppressor / physiology
  • Humans
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / genetics*
  • RNA, Double-Stranded / administration & dosage
  • RNA, Double-Stranded / genetics
  • RNA, Small Interfering / administration & dosage
  • RNA, Small Interfering / genetics*
  • RNA, Small Untranslated / administration & dosage
  • RNA, Small Untranslated / genetics
  • Transcription Factors / genetics

Substances

  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, human
  • RNA, Double-Stranded
  • RNA, Small Interfering
  • RNA, Small Untranslated
  • Transcription Factors