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RNAi - Technologies, Markets and Companies


News provided by

Reportlinker

Dec 29, 2011, 09:44 ET

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NEW YORK, Dec. 29, 2011 /PRNewswire/ -- Reportlinker.com announces that a new market research report is available in its catalogue:

RNAi - technologies, markets and companies

http://www.reportlinker.com/p0203551/RNAi---technologies-markets-and-companies.html#utm_source=prnewswire&utm_medium=pr&utm_campaign=Biological_Therapy

Summary

RNA interference (RNAi) or gene silencing involves the use of double stranded RNA (dsRNA). Once inside the cell, this material is processed into short 21-23 nucleotide RNAs termed siRNAs that are used in a sequence-specific manner to recognize and destroy complementary RNA. The report compares RNAi with other antisense approaches using oligonucleotides, aptamers, ribozymes, peptide nucleic acid and locked nucleic acid.

Various RNAi technologies are described, along with design and methods of manufacture of siRNA reagents. These include chemical synthesis by in vitro transcription and use of plasmid or viral vectors. Other approaches to RNAi include DNA-directed RNAi (ddRNAi) that is used to produce dsRNA inside the cell, which is cleaved into siRNA by the action of Dicer, a specific type of RNAse III. MicroRNAs are derived by processing of short hairpins that can inhibit the mRNAs. Expressed interfering RNA (eiRNA) is used to express dsRNA intracellularly from DNA plasmids.

Delivery of therapeutics to the target tissues is an important consideration. siRNAs can be delivered to cells in culture by electroporation or by transfection using plasmid or viral vectors. In vivo delivery of siRNAs can be carried out by injection into tissues or blood vessels or use of synthetic and viral vectors.

Because of its ability to silence any gene once the sequence is known, RNAi has been adopted as the research tool to discriminate gene function. After the genome of an organism is sequenced, RNAi can be designed to target every gene in the genome and target for specific phenotypes. Several methods of gene expression analysis are available and there is still need for sensitive methods of detection of gene expression as a baseline and measurement after gene silencing. RNAi microarray has been devised and can be tailored to meet the needs for high throughput screens for identifying appropriate RNAi probes. RNAi is an important method for analyzing gene function and identifying new drug targets that uses double-stranded RNA to knock down or silence specific genes. With the advent of vector-mediated siRNA delivery methods it is now possible to make transgenic animals that can silence gene expression stably. These technologies point to the usefulness of RNAi for drug discovery.

RNAi can be rationally designed to block the expression of any target gene, including genes for which traditional small molecule inhibitors cannot be found. Areas of therapeutic applications include virus infections, cancer, genetic disorders and neurological diseases. Research at academic centers that is relevant to RNAi-based therapeutics is mentioned.

Regulatory, safety and patent issues are discussed. Side effects can result from unintended interaction between an siRNA compound and an unrelated host gene. If RNAi compounds are designed poorly, there is an increased chance for non-specific interaction with host genes that may cause adverse effects in the host. However, there are no major safety concerns and regulations are in preliminary stages as the clinical trials are still ongoing and there are no marketed products. Many of the patents are still pending.

The markets for RNAi are difficult to define as no RNAi-based product is approved yet but several are in clinical trials. The major use of RNAi reagents is in research but it partially overlaps that of drug discovery and therapeutic development. Various markets relevant to RNAi are analyzed from 2011 to 2021. Markets are also analyzed according to breakdown of technologies and use of siRNAs, miRNAs, etc.

Profiles of 161 companies involved in developing RNAi technologies are presented along with 217 collaborations. They are a mix of companies that supply reagents and technologies (nearly half of all) and companies that use the technologies for drug discovery. Out of these, 33 are developing RNAi-based therapeutics and 30 are involved in microRNAs. The bibliography contains selected 600 publications that are cited in the report. The text is supplemented with 35 tables and 10 figures.

Table of Contents

0. Executive Summary 15

1. Technologies for suppressing gene function 17

Introduction 17

DNA transcription 17

RNA 17

Non-coding RNA 17

RNA research and potential applications 18

Role of RNA in regulation of the dihydrofolate reductase gene 19

Gene regulation 19

Post-transcriptional regulation of gene expression 20

Alternative RNA splicing 21

Technologies for gene suppression 21

Antisense oligonucleotides 21

Transcription factor decoys 22

Aptamers 22

Ribozymes 23

Aptazymes 23

RNA aptamers vs allosteric ribozymes 24

RNA Lasso 24

Peptide nucleic acid 24

PNA-DNA chimeras 25

Locked nucleic acid 25

Gene silencing 25

Post-transcriptional gene silencing 26

TargeTronÔ technology for gene knockout 26

Definitions and terminology of RNAi 26

RNAi mechanisms 27

Non-promoter-associated small RNAs 29

Piwi-interacting RNAs in germ cell development 30

Relation of RNAi to junk DNA 30

RNA editing and RNAi 31

Historical landmarks in the development of RNAi 31

2. RNAi Technologies 33

Introduction 33

Comparison of antisense and RNAi 33

Advantages of antisense over siRNAs 33

Advantages of siRNAs over antisense 34

RNA aptamers vs siRNA 34

RNA Lassos versus siRNA 34

Concluding remarks on antisense vs RNAi 35

ssRNAi 35

Antisense vs DNP-ssRNA and DNP-siRNA 35

LNA and RNAi 36

LNA for gene suppression 36

Comparison of LNA and RNAi 37

Use of siLNA to improve siRNA 37

RNAi versus small molecules 37

RNAi in vivo 37

Cre-regulated RNAi in vivo 38

RNAi kits 38

ShortCut™ RNAi Kit 38

HiScribe™ RNAi Transcription Kit 39

pSUPER RNAi system 39

Si2 Silencing Duplex 40

Techniques for measuring RNAi-induced gene silencing 40

Application of PCR in RNAi 40

Real-time quantitative PCR 41

Assessment of the silencing effect of siRNA by RT-PCR 41

Fluorescence resonance energy transfer probe for RNA interactions 42

Bioinformatics tools for design of siRNAs 42

Random siRNA design 42

Rational siRNA design 43

The concept of pooling siRNAs 44

Criteria for rational siRNA design 44

BLOCK-iT RNAi Designer 44

QIAGEN's 2-for-Silencing siRNA Duplexes 45

Designing vector-based siRNA 45

iRNAChek for designing siRNA 45

TROD: T7 RNAi Oligo Designer 45

siDirect: siRNA design software 46

Prediction of efficacy of siRNAs 46

Algorithms for prediction of siRNA efficacy 46

siRNA databases 46

Production of siRNAs 47

Chemical synthesis of short oligonucleotides 47

In vitro transcription 47

Generation of siRNAs in vivo 48

UsiRNAs 48

siRNA:DNA hybrid molecules 49

Chemical modifications of siRNAs 49

Sugar modifications of siRNA 49

Phosphate linkage modifications of siRNA 49

Modifications to the siRNA overhangs 50

Modifications to the duplex architecture 50

Applications of chemical modification of siRNAs 50

Synthetic RNAs vs siRNAs 51

Specificity of siRNAs 51

Asymmetric interfering RNA 52

Genome-wide data sets for the production of esiRNAs 52

ddRNAi for inducing RNAi 52

ddRNAi technology 52

Advantages of ddRNAi over siRNA 53

Short hairpin RNAs 54

siRNA versus shRNA 54

Circular interfering RNA 55

Expressed interfering RNA 56

RNA-induced transcriptional silencing complex 56

Inhibition of gene expression by antigene RNA 57

RNAi vs mRNA modulation by small molecular weight compounds 57

3. MicroRNA 59

Introduction 59

miRNA and RISC 61

Role of the microprocessor complex in miRNA 61

miRNAs compared to siRNAs 62

miRNA and stem cells 63

Influence of miRNA on stem cell formation and maintenance 63

Role of miRNAs in gene regulation during stem cell differentiation 63

miRNA databases 64

Sanger miRBase miRNA sequence database 64

Mapping miRNA genes 64

A database of ultraconserved sequences and miRNA function 65

A database for miRNA deregulation in human disease 65

An database of miRNA-target interactions 66

Role of miRNA in gene regulation 66

Control of gene expression by miRNA 67

miRNA-mediated translational repression involving Piwi 67

Transcriptional regulators of ESCs control of miRNA gene expression 67

Mechanism of miRNAs-induced silencing of gene expression 67

miRNA diagnostics 68

Biochemical approach to identification of miRNA 68

Computational approaches for the identification of miRNAs 69

LNA probes for exploring miRNA 69

Microarrays for analysis of miRNA gene expression 69

Microarrays vs quantitative PCR for measuring miRNAs 70

miRNAs as biomarkers of hepatotoxicity 70

Modification of in situ hybridization for detection of miRNAs 71

Nuclease Protection Assay to measure miRNA expression 71

Real-time PCR for expression profiling of miRNAs 71

Targeting of miRNAs with antisense oligonucleotides 72

Silencing miRNAs by antagomirs 72

New tools for miRNA silencing 72

Use of HAPIscreen for identification of aptamers against pre-miRNAs 73

miRNA-regulated lentiviral vectors 73

miRNAs as drug targets 73

miRNAs as targets for antisense drugs 74

Challenges facing use of miRNAs as drug targets 74

Target specificity of miRNAs 74

Prediction of miRNA targets 75

Role of miRNA in human health and disease 75

Role of miRNAs in regulation of hematopoiesis 76

Role of miRNA depletion in tissue regeneration 76

Role of miRNA in regulation of aging 77

Role of miRNA in inflammation 77

Role of miRNAs in regulation of immune system 77

Role of miRNA in the cardiovascular system 77

Role of miRNAs in development of the cardiovascular system 78

Role of miRNAs in angiogenesis 78

Role of miRNAs in cardiac hypertrophy and failure 78

Role of miRNAs in conduction and rhythm disorders of the heart 79

Diagnostic and prognostic value of miRNAs in acute coronary syndrome 79

miRNA-based approaches for reduction of hypercholesterolemia 80

miRNA-based approach for restenosis following angioplasty 80

miRNA gene therapy for ischemic heart disease 80

miRNAs as therapeutic targets for cardiovascular diseases 81

Concluding remarks and future prospects of miRNA in the cardiovascular system 81

Role of miRNAs in the nervous system 81

miRNAs and addiction 82

miRNAs in neurodegenerative disorders 82

miRNAs as biomarkers of Alzheimer's disease 83

miRNAs in Huntington's disease 83

miRNA malfunction in spinal motor neuron disease 83

miRNAs and retinal neurodegenerative disorders 84

miRNA and schizophrenia 84

Role of miRNA in viral infections 84

Role of miRNA in HSV-1 latency 84

miRNA and autoimmune disorders 85

miRNA in rheumatoid arthritis 85

miRNA in systemic lupus erythematosus 85

miRNAs in gastrointestinal disorders 86

miRNA-based therapies for the irritable bowel syndrome 86

miRNA and skin disorders 86

Role of miRNA in inflammatory skin disorders 86

Role of miRNAs in cancer 86

miRNAs linked to the initiation and progression of cancer 86

Oncomirs 87

Linking miRNA sequences to cancer using RNA samples 88

Role of miRNAs in viral oncogenesis 88

miRNA genes in cancer 88

miRNAs interaction with p53 89

miRNAs, embryonic stem cells and cancer 89

miRNAs and cancer metastases 90

Role of miRNAs in cancer diagnosis 91

Cancer miRNA signature 91

miRNA biomarkers in cancer 91

Diagnostic value of miRNA in cancer 92

Prognostic value of miRNA in cancer 92

miRNAs as basis of cancer therapeutics 92

Antisense oligonucleotides targeted to miRNA 92

Delivery of miRNA mimetics in Cancer 93

Role of miRNAs in adoptive immunotherapy of cancer 93

Restoration of tumor suppressor miRNA may inhibit cancer 93

Role of miRNAs in various cancers 94

miRNA and brain cancer 94

miRNA and breast cancer 95

miRNA and colorectal cancer 95

miRNA and gastrointestinal cancer 95

miRNA and hematological malignancies 96

miRNA and hepatocellular carcinoma 97

miRNA and lung cancer 97

miRNA and nasopharyngeal carcinoma 98

miRNA and ovarian cancer 99

miRNA and pancreatic cancer 99

miRNA and prostatic cancer 100

miRNA and thyroid cancer 100

Future prospects of miRNA 101

Companies involved in miRNA 101

4. Methods of delivery in RNAi 103

Introduction 103

Methods of delivery of oligonucleotides 103

Oral and rectal administration 104

Pulmonary administration 104

Targeted delivery to the CNS 104

High flow microinfusion into the brain parenchyma 105

Intracellular guidance by special techniques 105

Biochemical microinjection 106

Liposomes-mediated oligonucleotide delivery 106

Polyethylenimine-mediated oligonucleotide delivery 106

Delivery of TF Decoys 106

Biodegradable microparticles 107

Microparticles 107

Nanoparticles 107

Self-delivering rxRNA 107

siRNA delivery technologies 108

Local delivery of siRNA 109

In vivo delivery of siRNAs by synthetic vectors 109

Intracellular delivery of siRNAs 109

Delivery of siRNAs with aptamer-siRNA chimeras 110

MPG-based delivery of siRNA 110

Nanoparticles for intracellular delivery of siRNA 110

Protamine-antibody fusion proteins for delivery of siRNA to cells 110

Protein transduction domains 111

Phosphorothioate stimulated cellular delivery of siRNA 111

Targeted delivery of siRNAs by lipid-based technologies 111

Delivery of siRNA-lipoplexes 112

Lipidoids for delivery of siRNAs 112

NeoLipid™ technology 113

siFECTamineÔ 113

Systemic in vivo delivery of lipophilic siRNAs 113

Systemic delivery of siRNAi by lipid nanoparticles 113

Electroporation 114

Nucleofactor technology 114

Visualization of electrotransfer of siRNA at single cell level 115

Intravascular delivery of siRNA 115

27mer siRNA duplexes for improved delivery and potency 116

TransIT-TKOÒ 116

DNA-based plasmids for delivery of siRNA 117

Convergent transcription 117

PCR cassettes expressing siRNAs 118

Genetically engineered bacteria for delivery of shRNA 118

Viral vectors for delivery of siRNA 118

Adenoviral vectors 118

Adeno-associated virus vectors for shRNA expression 119

Baculovirus vector 119

Lentiviral vectors 119

Retroviral delivery of siRNA 120

Transkingdom RNAi delivery by genetically engineered bacteria 121

Delivery of siRNA without a vector 121

Cell-penetrating peptides for delivery of siRNAs 121

Role of nanobiotechnology in siRNA delivery 122

Chitosan-coated nanoparticles for siRNA delivery 122

Cyclodextrin nanoparticles 122

Delivery of gold nanorod-siRNA nanoplex to dopaminergic neurons 123

Lipidic aminoglycoside as siRNA nanocarrier 123

Lipid nanoparticles-mediated siRNA delivery 123

Nanosize liposomes for delivery of siRNA 124

PAMAM dendrimers for siRNA delivery 124

Polyethylenimine nanoparticles for siRNA delivery 125

Polycation-based nanoparticles for siRNA delivery 125

Quantum dots to monitor siRNA delivery 126

Targeted delivery of siRNAs to specific organs 126

siRNA delivery to the CNS 126

siRNA delivery to the liver 127

siRNA delivery to the lungs 127

Control of RNAi and siRNA levels 127

siRNA pharmacokinetics in mammalian cells 128

Mathematical modeling for determining the dosing schedule of siRNA 128

Assessing siRNA pharmacodynamics in animal models 129

Research on siRNA delivery funded by the NIH 129

Companies involved in delivery technologies for siRNA 130

5. RNAi in Research 133

Introduction 133

Basic RNAi research 133

Antiviral role of RNAi in animal cells 133

Combination of siRNA with green fluorescent protein 133

Detection of cancer mutations 134

Genes and lifespan 134

Inducible and reversible RNAi 134

Loss-of-function genetic screens 134

Profiling small RNAs 135

RNAi for research in neuroscience 135

RNAi and environmental research 136

Silencing snoRNA genes 136

Study of signaling pathways 136

Transgenic RNAi 137

Use of RNAi to study insulin action 137

Applied RNAi research 137

RNAi for gene expression studies 137

Microarrays for measuring gene expression in RNAi 137

RNAi for functional genomic analysis 138

RNAi studies on C. elegans 138

RNAi studies on Drosophila 139

RNAi in planaria 140

Testing the specificity of RNAi 140

Tissue-specific RNAi 140

siRNA-mediated gene silencing 141

RNAi libraries 141

Universal plasmid siRNA library 142

pDual library using plasmid vector 142

pHippy plasmid vector library 143

siRNA libary including miRNAs 143

siRNA libraries using pRetroSuper vector 143

siRNA produced by enzymatic engineering of DNA 143

shRNA libraries 144

Enzymatic production of RNAi library 145

RNAi and alternative splicing 145

RNAi in animal development 145

RNAi for creating transgenic animals 146

RNAi for creating models of neurological disorders 146

Research support for RNAi in US 147

RNAi for toxicogenomics 147

Role of RNAi in the US biodefense research 147

The RNAi Consortium 147

Research support for RNAi in Europe 148

European Union for RNA Interference Technology 148

Research support of RNAi 149

Role of RNAi in MitoCheck project 149

RNAi Global Initiative 150

SIROCCO project 151

6. RNAi in drug discovery 153

Basis of RNAi for drug discovery 153

RNAi for identification of genes as therapeutic targets 153

Role of siRNAs in drug target identification 154

Use of a genome-wide, siRNA library for drug discovery 154

Use of arrayed adenoviral siRNA libraries for drug discovery 154

RNAi as a tool for assay development 155

Targeting human kinases with an siRNAi library 155

Challenges of drug discovery with RNAi 155

Express TrackSM siRNA Drug Discovery Program 156

Genome-wide siRNA screens in mammalian cells 156

PhenomicID™ 156

Natural antisense and ncRNA as drug targets 157

RNAi for target validation 157

Delivering siRNA for target validation in vivo 157

Off-target effects of siRNA-mediated gene silencing 159

Bioinformatic approach to off-target effects 160

Validation of oncology targets discovered through RNAi screens 160

Selection of siRNA versus shRNA for target validation 161

Application of RNAi to the druggable genome 161

Application of siRNA during preclinical drug development 161

siRNAs vs small molecules as drugs 162

siRNAs vs antisense drugs 162

RNAi technology in plants for drug discovery and development 163

Application of RNAi to poppy plant as source of new drugs 163

7. Therapeutic applications of RNAi 165

Introduction 165

Potential of RNAi-based therapies 166

In vitro applications of siRNA 166

In vivo applications of RNAi 167

RNAi and cell therapy 167

Gene inactivation to study hESCs 168

RNAi and stem cells 168

Cell therapy for immune disorders 169

RNAi gene therapy 169

Drug-inducible systems for control of gene expression 169

Potential side effects of RNAi gene therapy 170

Systemic delivery of siRNAs 170

In vivo RNAi therapeutic efficacy in animal models of human diseases 171

Virus infections 171

RNAi approaches to viral infections 172

Delivery of siRNAs in viral infections 173

RNAi applications in HIV 173

A multiple shRNA approach for silencing of HIV-1 174

Anti-HIV shRNA for AIDS lymphoma 174

Aptamer-mediated delivery of anti-HIV siRNAs 174

Bispecific siRNA constructs 174

Role of the nef gene during HIV-1 infection and RNAi 175

siRNA-directed inhibition of HIV-1 infection 175

Synergistic effect of snRNA and siRNA 176

Targeting CXCR4 with siRNAs 176

Targeting CCR5 with siRNAs 176

Concluding remarks on RNAi approach to HIV/AIDS 177

Influenza 177

Inhibition of influenza virus by siRNAs 178

Delivery of siRNA in influenza 179

Challenges and future prospects of siRNAs for influenza 179

Respiratory syncytial and parainfluenza viruses 180

Coronavirus/severe acute respiratory syndrome 181

Herpes simplex virus 2 181

Hepatitis B 181

Hepatitis C virus 182

Cytomegalovirus 183

Ebola virus 184

siRNA vs antisense oligonucleotides for viral infections 184

siRNA against methicillin-resistant S. aureus 185

RNAi-based rational approach to antimalarial drug discovery 185

Inhibiting the growth of malarial parasite by heme-binding DNA aptamers 185

siRNA-based antimalarial therapeutics 186

RNAi applications in oncology 186

Allele-specific inhibition 187

Drug delivery issues in managing cancer by RNAi approach 187

Inhibition of oncogenes 188

Modification of alternative splicing in cancer 189

Onconase 189

Overcoming drug resistance in cancer 190

Targeting fusion proteins in cancer 191

Increasing chemosensitivity by RNAi 191

RNAi approach to study TRAIL 191

RNAi-based logic circuit for identification of specific cancer cells 192

siRNAs for anticancer drug discovery 192

siRNAs for inducing cancer immunity 193

siRNAs for inhibition of angiogenesis 193

siRNA targeting the R2 subunit of ribonucleotide reductase 194

siRNA for cancer chemoprevention 194

siHybrids vs siRNAs as anticancer agents 194

Nanobiotechnology-based delivery of siRNAs 195

Lipid nanoparticle-based delivery of anticancer siRNAs 195

Minicells for targeted delivery of nanoscale anticancer therapeutics 195

Nanoimmunoliposome-based system for targeted delivery of siRNA 196

Polymer nanoparticles for targeted delivery of anticancer siRNA 196

RNA nanotechnology for delivery of cancer therapeutics 197

Targeted delivery of a nanoparticle-siRNA complex in cancer patients 197

RNAi-based treatment of various cancer types 198

RNAi-based therapy of brain cancer 198

RNAi in breast cancer 199

RNAi for enhancing hyperthermia/chemotherapy in cervical cancer 200

RNAi and colorectal cancer 200

RNAi and Ewing's sarcoma 201

RNAi and leukemias 201

RNAi and lung cancer 202

RNAi and melanoma 202

RNAi and pancreatic cancer 203

RNAi and prostate cancer 203

Genetic disorders 203

RNAi for skin disorders 204

Experimental studies for RNAi applications in skin disorders 204

Clinical applications of RNAi in skin disorders 205

Pachyonychia congenita 205

Neurological disorders 205

RNAi for neurodegenerative disorders 206

Alzheimer's disease 207

Parkinson's disease 208

Amyotrophic lateral sclerosis 208

Prion diseases 209

Polyglutamine-induced neurodegeneration 210

Fragile X syndrome and RNAi 210

RNAi-based therapy for Huntington's disease 211

Combination of RNAi and gene therapy to prevent neurodegenerative disease 212

Role of RNAi in pain therapy 212

Role of RNAi in repair of spinal cord injury 213

Role of RNAi in treatment of multiple sclerosis 213

siRNA for Duchenne muscular dystrophy 213

siRNA for dystonia 214

RNAi in ophthalmology 214

Age related macular degeneration 214

Current treatment of AMD 214

RNAi-based treatments for AMD 215

Diabetic retinopathy 216

Retinitis pigmentosa 217

RNAi and metabolic disorders 218

RNAi and obesity 218

Genes and regulation of body fat 218

RNAi and diabetes 218

Regulation of insulin secretion by a miRNA 218

RNAi for study of genes in animal models of diabetes 219

RNAi for drug discovery in diabetes 219

RNAi for treating liver dysfunction in diabetes 220

siRNAs for study of glucose transporter 220

siRNAs for targeting adipose inflammation in diabetes and obesity 221

RNAi in hematology 221

Stem cell-based gene therapy and RNAi for sickle cell disease 221

RNAi and disorders of the immune system 222

siRNA applications in immunology 222

Use of RNAi in transplantation 223

RNAi for cardiovascular disorders 224

RNAi for hypercholesterolemia 224

siRNA targeting NADPH oxidase in cardiovascular diseases 225

siRNA for study and treatment of ischemia-reperfusion injury 225

RNAi in respiratory disorders 226

siRNA for cystic fibrosis 226

siRNA for asthma 226

RNAi for musculoskeletal disorders 226

RNAi for rheumatoid arthritis 226

RNAi for bone disorders 227

RNAi for treatment of osteoporosis 228

Research relevant to RNAi-based therapies at academic institutes 228

Laboratory of RNA Molecular Biology, The Rockefeller University 228

RNAi Center, La Jolla Institute for Allergy & Immunology 228

Clinical trials of RNAi-based therapies 229

Improving efficacy of siRNAs for clinical trials by improved delivery 230

Role of RNAi in development of personalized medicine 230

Future prospects of RNAi 231

Challenges for the development of RNAi-based therapeutics 231

8. Safety, regulatory and patent issues 233

Introduction 233

Limitations and drawbacks of RNAi 233

Adverse effects of RNAi 233

Effect of siRNAs on interferon response 234

Detection of interferon response 234

Prevention of the interferon response in RNAi 235

Overcoming the innate immune response to siRNAs 235

Toxicity associated with RNAi 236

Selection of siRNAs to improve specificity and efficacy 236

Regulatory issues relevant to RNAi 236

RNAi patents 237

Companies with strong patent position 237

Alnylam 237

Benitec 240

Intradigm 240

Quark Pharmaceuticals 240

Sirna Therapeutics 241

9. Markets for RNAi Technologies 243

Introduction 243

Current and future market potential for RNAi technologies 243

RNAi reagents 244

siRNA markets 244

RNAi-based drug discovery and target validation 244

RNAi-based development of therapeutics 244

RNAi market potential according to therapeutic areas 245

Market for viral infections 245

Market for cancer 246

Market for age related macular degeneration 246

Unmet needs in RNAi 246

Strategies for marketing RNAi 247

Choosing optimal indications 247

Strategies according to the trends in healthcare in the next decade 248

Concluding remarks 249

10. Companies involved in RNAi Technologies 251

Introduction 251

Major players in RNAi 254

Profiles of companies 255

Collaborations 443

11. References 451

Tables

Table 1?1: Classification of small RNA molecules 27

Table 1?2: Mechanisms of small RNAs involved in gene silencing 28

Table 1?3: Historical landmarks in the evolution of RNAi 31

Table 2?1: RNAi versus small molecules 37

Table 2?2: Providers of software for siRNA design 43

Table 2?3: Methods for the production of siRNAs 47

Table 2?4: Advantages and limitations of methods of shRNA-derived siRNA knockdown 55

Table 2?5: Comparison of eiRNA with siRNA 56

Table 3?1: Methods for miRNA target prediction 75

Table 3?2: miRNA expression in neurodegenerative diseases 82

Table 3?3: Dysregulation of miRNA expression in epithelial cancers 87

Table 3?4: Companies involved in miRNA diagnostics and therapeutics 101

Table 4?1: Methods of delivery of oligonucleotides 103

Table 4?2: Methods of delivery of siRNA 108

Table 4?3: Companies developing siRNA delivery technologies 130

Table 5?1: RNAi libraries 141

Table 6?1: Delivery of siRNAs in vivo for target validation 158

Table 6?2: Selection of siRNA versus shRNA for target validation 161

Table 7?1: RNAi-based therapeutic approaches 166

Table 7?2: In vivo RNAi therapeutic efficacy in animal models of human diseases 171

Table 7?3: Inhibition of viral replication by RNAi 172

Table 7?4: Cancer-associated genes that can be targeted by RNAi 188

Table 7?5: Neurological disorders that have been studied by using RNAi 206

Table 7?6: Clinical trials of RNAi-based therapeutics 229

Table 9?1: RNAi markets according to technologies and reagents 2011-2021 243

Table 9?2: Markets for RNAi therapy for selected diseases: years 2011-2021 245

Table 10?1: RNAi reagent, technology and service companies 251

Table 10?2: Pharmaceutical companies using RNAi for drug discovery and development 252

Table 10?3: Biotechnology companies using RNAi for drug discovery and development 253

Table 10?4: Companies developing RNAi-based therapeutic products 254

Table 10?5: Major players in RNAi 254

Table 10?6: RNAi products of Benitec 275

Table 10?7: Proprietary reagents of ImuThes 330

Table 10?8: Product pipeline of Silence Therapeutics 412

Table 10?9: Collaborations in RNAi technologies 443

Figures

Figure 1?1: Relationship of DNA, RNA and protein in the cell 20

Figure 1?2: Schematic of suppression of gene expression by RNAi 28

Figure 2?1: Overview of ShortCut RNAi Kit 39

Figure 2?2: Gene silencing by RNAi induced with ddRNAi 53

Figure 3?1: A schematic miRNA pathway 59

Figure 3?2: Molecular mechanisms of miRNA generation 60

Figure 7?1: Targeting disease by RNAi 165

Figure 7?2: Role of RNAi in personalized medicine 231

Figure 8?1: Problems with use of synthetic siRNAs and measures to prevent them 234

Figure 9?1: Unmet needs in RNAi technologies 247

To order this report:

Biological Therapy Industry: RNAi - technologies, markets and companies

More  Market Research Report

Check our  Industry Analysis and Insights

CONTACT:
Nicolas Bombourg
Reportlinker
Email: [email protected]
US: (805)652-2626
Intl: +1 805-652-2626

SOURCE Reportlinker

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