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Targeting noncoding RNAs in disease
Brian D. Adams,1,2 Christine Parsons,3 Lisa Walker,4 Wen Cai Zhang,4 and Frank J. Slack4
1The RNA Institute, University at Albany, State University of New York, Albany, New York, USA.
2Investigative Medicine Program, Yale University Medical School, New Haven, Connecticut, USA.
3Department of Biochemistry, Bowdoin College, Brunswick, Maine, USA.
4Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Address correspondence to: Brian D. Adams, Research Faculty, The RNA Institute, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, USA. Or to: Brian D. Adams, Investigative Medicine Program, Yale University Medical School, 2 Church Street South, Suite 114, New Haven, Connecticut 06520, USA. Phone: 518.437.4447; E-mail: [email protected]. Or to: Frank J. Slack, Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, Massachusetts 02115, USA. Phone: 617.735.2601; E-mail: [email protected].
Authorship note: B.D. Adams and C. Parsons contributed equally to this work.
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1The RNA Institute, University at Albany, State University of New York, Albany, New York, USA.
2Investigative Medicine Program, Yale University Medical School, New Haven, Connecticut, USA.
3Department of Biochemistry, Bowdoin College, Brunswick, Maine, USA.
4Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Address correspondence to: Brian D. Adams, Research Faculty, The RNA Institute, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, USA. Or to: Brian D. Adams, Investigative Medicine Program, Yale University Medical School, 2 Church Street South, Suite 114, New Haven, Connecticut 06520, USA. Phone: 518.437.4447; E-mail: [email protected]. Or to: Frank J. Slack, Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, Massachusetts 02115, USA. Phone: 617.735.2601; E-mail: [email protected].
Authorship note: B.D. Adams and C. Parsons contributed equally to this work.
Find articles by Parsons, C. in: JCI | PubMed | Google Scholar
1The RNA Institute, University at Albany, State University of New York, Albany, New York, USA.
2Investigative Medicine Program, Yale University Medical School, New Haven, Connecticut, USA.
3Department of Biochemistry, Bowdoin College, Brunswick, Maine, USA.
4Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Address correspondence to: Brian D. Adams, Research Faculty, The RNA Institute, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, USA. Or to: Brian D. Adams, Investigative Medicine Program, Yale University Medical School, 2 Church Street South, Suite 114, New Haven, Connecticut 06520, USA. Phone: 518.437.4447; E-mail: [email protected]. Or to: Frank J. Slack, Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, Massachusetts 02115, USA. Phone: 617.735.2601; E-mail: [email protected].
Authorship note: B.D. Adams and C. Parsons contributed equally to this work.
Find articles by Walker, L. in: JCI | PubMed | Google Scholar
1The RNA Institute, University at Albany, State University of New York, Albany, New York, USA.
2Investigative Medicine Program, Yale University Medical School, New Haven, Connecticut, USA.
3Department of Biochemistry, Bowdoin College, Brunswick, Maine, USA.
4Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Address correspondence to: Brian D. Adams, Research Faculty, The RNA Institute, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, USA. Or to: Brian D. Adams, Investigative Medicine Program, Yale University Medical School, 2 Church Street South, Suite 114, New Haven, Connecticut 06520, USA. Phone: 518.437.4447; E-mail: [email protected]. Or to: Frank J. Slack, Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, Massachusetts 02115, USA. Phone: 617.735.2601; E-mail: [email protected].
Authorship note: B.D. Adams and C. Parsons contributed equally to this work.
Find articles by Zhang, W. in: JCI | PubMed | Google Scholar
1The RNA Institute, University at Albany, State University of New York, Albany, New York, USA.
2Investigative Medicine Program, Yale University Medical School, New Haven, Connecticut, USA.
3Department of Biochemistry, Bowdoin College, Brunswick, Maine, USA.
4Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Address correspondence to: Brian D. Adams, Research Faculty, The RNA Institute, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, USA. Or to: Brian D. Adams, Investigative Medicine Program, Yale University Medical School, 2 Church Street South, Suite 114, New Haven, Connecticut 06520, USA. Phone: 518.437.4447; E-mail: [email protected]. Or to: Frank J. Slack, Institute for RNA Medicine, Department of Pathology, Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, Massachusetts 02115, USA. Phone: 617.735.2601; E-mail: [email protected].
Authorship note: B.D. Adams and C. Parsons contributed equally to this work.
Find articles by Slack, F. in: JCI | PubMed | Google Scholar
Published March 1, 2017 - More info
J Clin Invest. 2017;127(3):761–771. https://doi.org/10.1172/JCI84424.
Copyright © 2017, American Society for Clinical Investigation
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Introduction
For decades, the central dogma that misregulated DNA, RNA, and proteins can result in disease states such as cancer has dominated our understanding of complex cellular processes. While many crucial, highly conserved metabolic and environmental protein-based feedback loops have been studied, a majority of these systems do not address the underlying genetic complexity associated with higher eukaryotic systems. This complexity is most likely derived from the noncoding RNA (ncRNA) portion of the genome, once thought of as “junk DNA.” In fact, approximately 98% of the human genome consists of noncoding DNA (1), and approximately 70% of the genome is actively transcribed, 2% of which codes for known protein-coding genes (2). Research over the last two decades revealed new classes of ncRNAs, including microRNAs (miRNAs), small nucleolar RNAs (snoRNAs), long ncRNAs (lncRNAs), and circular RNAs (circRNAs), all with different regulatory functions that effectively feed back into a larger RNA communication network that ultimately regulates the fundamental protein effectors of cellular function (Figure 1 and refs. 3–10).
Figure 1The complexity of noncoding RNA gene networks. In this scenario, four genes are transcribed. However, only the splice variants mRNA-1 and mRNA-2 encoded by gene A are translated into protein products. These protein products can be regulated by noncoding RNAs (ncRNAs) that are encoded by genes B, C, and D, which interact with gene A at the RNA level in what is referred to as an RNA language or RNA network. Gene B encodes miRNA, which can interact with mRNAs at their 3′-UTR. Gene C encodes long noncoding RNA (lncRNA), which can interact with the protein products of gene A or serve as a decoy for certain miRNAs. Gene D encodes circular RNA (circRNA), which can sponge or serve as a decoy for any RNA binding event that indirectly regulates gene A protein products, such as lncRNA or miRNA interactions.
The first observation that RNA interference (RNAi) was possible occurred in transgenic plants, where an attempt was made to alter flower color in Petunia hybrida by reducing the expression of chalcone synthase by single-stranded antisense RNA (11). Soon after, Fire, Mello, and colleagues reported that injection of short dsRNA into Caenorhabditis elegans resulted in robust gene silencing (12). These early antisense technologies, however, used an endogenous RNA-induced silencing pathway. This concept was realized when miRNAs were discovered in C. elegans (8). Subsequent research identified miRNAs as regulators of biological processes, including development, proliferation, apoptosis, and cell metabolism (4, 13–18). These endogenous small RNAs are transcribed by RNA polymerase II, 5′-capped, and 3′-polyadenylated, and undergo sequential processing in the nucleus and cytoplasm by the RNase III enzymes DROSHA and DICER to generate an approximately 19- to 22-nt mature miRNA (19–21). The miRNA guides RNA-induced silencing complex (RISC) to the 3′-UTR of target mRNAs via sequence complementarity, resulting in degradation/destabilization or translational repression (22, 23). miRNAs regulate more than 60% of human protein-coding genes (24), and aberrant miRNA expression can alter the translational landscape within a cell, leading to deleterious phenotypic outcomes or disease states (18).
Another subset of ncRNAs transcribed by RNA polymerase II are lncRNAs (8). These transcripts are greater than 200 nt in length and are found in sense or antisense orientation to protein-coding genes, or within intergenic regions. lncRNAs regulate gene expression through a number of mechanisms, including epigenetic regulation via chromatin remodeling, transcriptional activation or repression, posttranscriptional modification of mRNA, or modulation of protein activity. lncRNAs can serve as scaffolds that recruit RNA-binding proteins (RBPs) into spatial proximity to each other, and/or guide RBPs to DNA. lncRNAs also function as decoys to compete for and disrupt protein-binding interactions, or to sponge miRNAs away from their natural mRNA targets (8, 25, 26). The X-inactive–specific transcript (XIST), which produces an approximately 20-kb RNA, was the first lncRNA discovered, and functions to balance X chromosome gene expression by recruiting polycomb repressive complex 2 (PRC2) to the inactive X chromosome. SHARP, SAF-A, and LBR are also required for XIST-mediated transcriptional silencing (27). Efforts to understand the epigenetic regulation mediated by lncRNAs have led to the finding that GWAS identify cancer risk loci outside of protein-coding regions, such as PTCSC3 in papillary thyroid carcinoma and ANRIL in type 2 diabetes, indicating that aberrant expression of lncRNAs associates with disease states (28–30).
As the biological significance of both small and long ncRNAs is becoming increasingly appreciated, numerous efforts have been initiated to target these ncRNAs in disease. Here we discuss development of therapeutic tools to target miRNA and lncRNAs in disease, the implications of these trials, and how continued elucidation of the underlying biology will serve as the basis for more effective rationales for ncRNA drug design and delivery.
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General therapeutic strategies for ncRNA targeting and delivery
Essential RNA chemical modifications. As a class of molecules, miRNAs hold particular therapeutic potential because they regulate multiple gene targets within a particular signaling pathway, or a number of targets across several independent pathways (4, 18). Thus, the pleiotropic regulatory potential of miRNAs can alter cell growth and survival depending on the proper cell context, e.g., whether the miRNA targets functional pathways that are highly expressed in the specific cell or tissue of interest. Therefore, certain miRNAs may harbor stronger therapeutic effects when reintroduced or inhibited within a specific cell type. Efforts over the past decade have indicated that numerous miRNAs have the potential to become therapeutic targets, and the renewed interest in RNA therapeutics (31) has made it very likely that hundreds of novel RNA-based therapeutic agents may be developed within the next decade.
The current strategy to express or inhibit miRNA function involves delivering synthetic oligoribonucleotides (ORNs) that mimic the native miRNA duplex in cases in which miRNA overexpression is required, or generating a single-stranded antisense RNA to sequester the endogenous miRNA of interest for inhibition studies (Figure 2). As expected, use of unmodified ORNs encounters substantial stability and delivery barriers. To maintain RNA stability, modifications to protect ORNs against nucleases and enhance RNA binding affinity have been explored (32, 33). One of the first advancements was development of a 2′-O-methyl (2′-OMe) substitution in the sugar backbone of the RNA (34, 35), which significantly enhanced the stability of these RNAs in vitro. However, a variety of chemical modifications were developed over the past decade, including changes to the backbone structure of the ORN such as 2′-O-methoxyethyl (2′-MOE), 2′-fluoro, or locked nucleic acid (LNA) bases, along with oligomerization of the ORN with phosphorothioate linkages instead of a canonical phosphodiester bond (36–39). 2′-MOE– and LNA-based antisense oligonucleotide (ASO) strategies enhance RNA stability such that systemic delivery of these agents in vivo at doses of 10–20 mg/kg results in desired gene targeting within certain tissues (39, 40). Targeting moieties can also be directly conjugated to the ORN, such as N-acetylgalactosamine (GalNAc) for delivery to hepatocytes in liver disease. Regulus Therapeutics has developed an anti–miR-122 compound specifically for hepatitis C patients.
Figure 2Oligoribonucleotide modifications for therapeutic delivery. (A) Various oligoribonucleotide (ORN) modifications have been developed to improve RNA stability, including (i) substitutions of the 2′-OH of the ribose sugar, such as 2′-O-methyl (2′-OMe, light blue), 2′-O-methoxyethyl (2′-MOE, yellow), and 2′-fluoro (2′-F) substitutions (red); (ii) replacement of the phosphodiester linkage with a phosphorothioate (dark blue); (iii) locking of the conformation of the backbone with a methylene bridge using LNA modification (green); and (iv) DNA modification of the ribose sugar to a deoxyribose sugar (purple). (B) Examples of current modifications used in anti-miRNA ORN therapeutic strategies. Figure adapted with permission from Silence (ref. 33; Creative Commons user license available at http://creativecommons.org/licenses/by/2.0).
ORN modifications have been widely exploited for antisense approaches to sequester mature miRNAs. However, in thinking of methodologies to therapeutically reintroduce or re-express miRNAs, the available chemical modifications become rate-limiting. Synthetic miRNA duplexes must be stable and nuclease resistant, able to unwind to allow only mature guide strand loading into RISC, and have the guide strand properly recognize and bind its cognate mRNA target. Most chemical modifications involve addition of 2′-OMe groups across the passenger strand of the miRNA duplex, while 2′-OMe modifications can occur on the 3′ end of the mature miRNA strand (41). The 2′-OMe modification is sufficient to protect the ORN from degradation and immune detection and obviates the need for stable modifications, such as LNAs and phosphorothioate linkages, which might interfere with the required unwinding of the duplex while in RISC. Developing modified duplex RNAs that remain biologically active is a challenge, however. Attempts to deliver a single-stranded mature miRNA have failed (42), presumably because of its inability to load into RISC. Therefore, continued efforts are being undertaken to enhance the stability and cellular uptake of miRNA mimics for therapeutic applications.
RNA delivery vehicles. miRNA function is cell context dependent, and the ability to direct miRNA-based therapeutics to certain tissues remains a goal. Therefore, modifications are required to enhance cellular uptake of ORNs. ORNs with an electroneutral peptide-like backbone, such as peptide nucleic acids (PNAs), have been developed to silence miRNAs (43, 44). PNAs can be conjugated to cholesterol moieties to increase hydrophobicity, but also to cell-penetrating peptides to facilitate cellular uptake and enhanced tissue targeting. Adding lysine groups on PNAs can facilitate the endosomal release of PNA once taken up by target cells. Despite these advancements, a major impediment to RNA-based therapeutics is that ORN doses of more than 5 mg/kg are required before substantial therapeutic effects are observed in vivo, and these high doses pose risks of toxicity. Nanotechnology-based delivery strategies have significantly reduced the challenges of stability and target tissue specificity. These technologies allow RNA delivery at therapeutic doses of less than 2 mg/kg, reducing their toxicity profile (45). The most established nanodelivery agents used are lipid-based nanocarriers. These complexes are normally modified by PEGylation or through ionization to avoid unwanted aggregation in serum and bypass nonspecific tissue uptake. Cationic lipid complexes can also be decorated with tumor-targeting agents such as single-chain fragment variable (scFv) or transferrin (45, 46). Other lipid approaches involve neutral emulsion, where neutral phospholipids are used to package the miRNA, and therefore avoid issues of charge when attempting to deliver a highly polar RNA molecule across the cell membrane (47). This approach has proven successful for delivery of let-7 and miR-34a in preclinical KrasLSL-G12D lung cancer mouse models (47–49).
Numerous advances in delivery methodologies that do not rely on lipid-based approaches include polymer- and peptide-based systems. Poly(lactic-co-glycolic acid) (PLGA) nanoparticles can be used to deliver both siRNAs and charge-neutral PNA-modified miRNAs (50, 51). In addition to mitigating charge and electrostatic interactions that result in unfavorable miRNA delivery, PLGA nanoparticles can be decorated with surface peptides such as penetratin, to aid in the cellular uptake of the miRNA. Poly(amine-co-ester) terpolymer (PACE) nanoparticles are also attractive delivery platforms composed of a biodegradable and nontoxic polymer. They release therapeutic payloads gradually over time and can be coated with molecules such as polyE-mRGD to improve tumor targeting (52, 53). Additional delivery approaches include direct ORN conjugation using peptides such as pH low insertion peptide (pHLIP), which can deliver anti–miR-155 PNA to mice harboring B cell lymphomas in a pH-dependent manner (54, 55). Use of tumor-specific aptamers, small nucleic acids whose 3D structure binds to specific cell surface proteins identified by systematic evolution of ligands by exponential enrichment (SELEX), is also used to improve targeting of PNAs (56, 57). Importantly, many of these nanoparticle delivery methods are safe and biodegradable, indicating that they could rapidly be developed into “next-generation” miRNA therapeutics for clinical testing (Table 1 and Figure 3).
Figure 3Delivery vehicles/carriers for ncRNAs. The images depict the various delivery methodologies described in Table 1. Peptide nucleic acid (PNA) approaches (A) and lipid-based nanocarriers (B) are the most well-characterized delivery methods for RNA. Recently, new carriers have been developed, including poly(lactic-co-glycolic acid)–coated (PLGA-coated) nanoparticles (C), poly(amine-co-esters) such as PACE (D), and pH-sensitive peptides such as pHLIP (E).
New tools for lncRNA delivery. lncRNAs function as decoys, regulators of translation, and modular scaffolds that guide chromatin-modifying enzymes to specific genomic loci (8). lncRNAs are an attractive class of therapeutic target given the tight transcriptional regulation, tissue-specific expression, and dysregulation in disease. Associations of HOTAIR in breast cancer (58, 59) as well as MALAT1 in metastatic lung cancer (60, 61) are notable examples of this relationship. The first evidence that modulating lncRNAs or using their flanking regulatory regions could have therapeutic value originated from studies of the H19 gene, an lncRNA with oncogenic properties that is highly expressed in a wide range of tumors. Intratumoral injection of plasmids expressing diphtheria toxin under control of the H19 promoter led to tumor reduction in bladder cancer xenograft mouse models (62). From this work, several phase I/II clinical trials have been initiated to treat patients with bladder, ovarian, and pancreatic cancer. Therefore, there has been excitement over the prospect of developing therapeutic tools to modulate misregulated lncRNAs in disease.
While lncRNAs can be found in the cytoplasm, they are predominantly nuclear (63). Therefore, modified ASOs have been used in an effort to target the lncRNA in the nuclear compartment to initiate RNase H–dependent degradation of the particular target lncRNA. Continued advancement of this technology includes the use of 2′-OMe RNA and LNA modifications at both the 5′ and the 3′ end of the ASO to protect against nuclease activity (64, 65). Despite improvements, the highly structured nature of lncRNAs can preclude ASO binding to a predicted site within the lncRNA molecule. While one solution is to generate many siRNAs to a particular lncRNA, the cost of assessing off-target effects for each molecule attempted can be prohibitive.
Another approach to modulate lncRNA expression in cells is to target promoter regions of genes. A majority of gene loci contain promoter-associated RNA (pRNA) transcripts that are transcribed in the sense orientation just upstream of an mRNA or lncRNA transcriptional start site (66, 67). pRNAs function as cis-regulatory elements by keeping the surrounding chromatin in an epigenetically active state. The use of ASOs or LNAs directed toward these pRNAs induces the recruitment of the nuclear RISC complex and a subsequent remodeling of the local chromatin (59). This involves recruitment of HDAC1, EZH2, and DNMT3A, which promotes enrichment of silent-state chromatin modifications, heterochromatin formation, and ultimately transcriptional gene silencing.
Although lncRNAs represent appealing pharmacological and therapeutic targets, inhibiting lncRNAs in vivo remains a challenge. Many limitations of delivering ASOs for lncRNAs are similar for all RNAi-based therapies. However, one tractable approach has been the use of small molecules that disrupt lncRNA-chromatin–modifying complexes to alter the epigenetic state of the target cell. It is well accepted that lncRNAs can regulate JARID2 and EZH2 (68), and if small molecules can be developed to target the binding cleft between the lncRNA and its protein-binding partner, these interactions may be disrupted. Similar approaches have been used for targeting miRNA function or disrupting the miRNA processing machinery (69–71). Taken together, these delivery efforts, along with further elucidation of lncRNA regulatory mechanisms, will ultimately lead to the development of effective therapeutic strategies that target lncRNAs in vivo.
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The role of ncRNAs in chronic disease
Development of ncRNA-based therapies could be considered a novel tool in treating a number of chronic diseases. For instance, protein products that are known culprits of the disease (e.g., MYC in cancer) have proven difficult to target (72). The development of RNAi-based drugs enabled highly specific targeting of genes of interest at the mRNA level. An extension of RNAi-based therapies is the ability to target the endogenous ncRNA transcriptome within a particular disease. Indeed, aberrant miRNA and lncRNA expression has been linked to a number of chronic illnesses, from heart disease to diabetes to cancer. Given the cell-specific context in which most ncRNAs operate, identifying the key misregulated ncRNAs within a particular disease context will lead to identification of ncRNA candidates for therapeutic targeting (Table 2).
ncRNAs support development of diabetes. Investigators have elucidated that ncRNAs are key players in metabolic pathways that support development of both type 1 and type 2 diabetes. Mice with an inducible β cell deletion of Dicer harbor a diabetic phenotype due to a reduction in insulin production, despite normal islet architecture (73). Loss of miR-26a, miR-148, miR-182, and miR-200, among other miRNAs, may be responsible for the reduced insulin phenotype, as these miRNAs positively regulate insulin transcription. A more actionable therapeutic target is miR-375, given its high abundance in pancreatic β cells. Modulation of miR-375 activity by 2′-OMe, ORN knockdown, or recombinant adenovirus overexpression in MIN6 cells, an insulin-secreting glucose-responsive pancreatic β cell line, alters glucose-stimulated insulin secretion and exocytosis through a novel pathway involving myotrophin (encoded by Mtpn) (74). miR-375 KO mice are hyperglycemic owing to decreased pancreatic β cell mass secondary to reduced proliferation, while in leptin KO mice, miR-375 levels are elevated and correlate with increased β cell mass (75). Clinically, miR-375 shows potential as a biomarker, as it is overexpressed in the serum of type 2 diabetic patients (76), and circulating miR-375 levels dramatically increase in mice before the onset of hyperglycemia (77). Therefore, while miR-375 is itself essential for normal glucose homeostasis and β cell turnover, dampening the effects of aberrant miR-375 expression in hyperglycemic patients represents a viable therapeutic strategy.
Despite preclinical evidence for use of certain miRNAs in the treatment of diabetes, Regulus Therapeutics has developed lead compounds such as RG-125(AZD4076), a GalNAc-conjugated anti–miR-103/107 ORN that can improve insulin sensitivity in preclinical mouse models. Use of anti–miR-103/107 and transient adenovirus-mediated expression of miR-103/107 in Mir103-transgenic mice was sufficient to induce an impairment of glucose homeostasis and alter insulin sensitivity (78, 79). Use of RG-125(AZD4076) in a diet-induced obesity model promoted reduced fasting blood glucose and plasma insulin levels as well as enhanced glucose tolerance, suggesting that miR-103/107 plays a central role in insulin sensitivity. AstraZeneca purchased RG-125(AZD4076) from Regulus, and together these companies are developing the compound to treat nonalcoholic steatohepatitis in patients with type 2 diabetes (80).
ncRNAs and the aging heart. ncRNAs control important processes in cardiac development and physiology, and aberrant expression of these ncRNAs have been linked to cardiovascular disease. α-MHC-Cre–mediated deletion of Dicer results in postnatal lethality due to cardiomyopathy (81), and a series of miRNAs abundantly expressed in striated muscle (myomiRs) are thought to be crucial regulators of cardiomyocyte proliferation, morphogenesis, and remodeling (82, 83). Inhibition of one of these myomiRs, miR-208a, by systemic delivery of antisense ORNs can improve cardiac function and survival during hypertension-induced heart failure in Dahl hypertensive rats (84). Importantly, approximately 80% of mice harboring a homozygous deletion of Mir208a had significant disruption of normal electrical conductivity resulting in atrial fibrillation (85). Therefore, proper dosing strategies will be required in nonhuman primates before therapeutic approaches are implemented.
miRNA profiling also indicated that members of the miR-15 family, including miR-195, miR-15a, miR-16, and miR-497, were important regulators of postnatal cardiomyocyte mitotic arrest by controlling cell cycle regulators, including Chek1. miR-15a is also upregulated during cardiac ischemia and heart failure (84). rAAV9-mediated delivery of anti–miR-15a, which has been used to deliver siRNAs to cardiac tissue in rats (85) and is a safe and effective delivery method widely used in clinical trials, may be an approach to alleviate the pathological hypertrophy and fibrosis associated with reduced cardiac function and failure. However, miRagen Therapeutics is currently in the preclinical stage of development of MGN-1374, an LNA-based anti–miR-15/195 compound (86). MGN-1374 was shown to enhance heart function and promote cardiomyocyte proliferation in murine and porcine models (87), indicating that this compound has potential to move forward for phase I trials.
lncRNAs are also associated with cardiac disease and could be targeted by standard ORN approaches. The lncRNA ANRIL was identified in large-scale GWAS for coronary artery disease (88) and is expressed in vascular endothelial and coronary smooth muscle cells (89). ANRIL may regulate the INK4a/b locus by recruiting PRC2 to impose a repressive chromatin state, thereby altering the senescent state of cells (90). It is not clear whether overexpression or knockdown of ANRIL would affect cardiomyocytes; therefore, the therapeutic augmentation of cardiac function by targeting of ANRIL during ischemic events is unclear. It will be important to elucidate the mechanisms of lncRNAs in other cardiac injury models, such as chemotherapy-induced cardiotoxicity, or inflammation-mediated ischemia, before fully pursuing lncRNA-based therapeutic strategies.
ncRNAs in neurogenesis and Alzheimer’s disease. Within the CNS, ncRNAs are expressed in specific spatiotemporal patterns and play a crucial role in buffering gene products along neuronal processes and synaptic junctions (91, 92). Improper integration of this information, perhaps through loss of the regulatory networks imparted by ncRNAs, can result in disease pathogenesis. For instance, ATXN8OS, an antisense RNA that encodes a CUG repeat, has been implicated in spinocerebellar ataxia type 8 (SCA8). SCA8 is an autosomal dominant disorder thought to be caused by a polyglutamine repeat expansion within the ATXN8 gene (93, 94). However, transgenic mice expressing ATXN8OS harbor dysregulated muscleblind-like splicing regulator 1–mediated pre-mRNA splicing. It would be interesting if a siRNA-based therapeutic strategy could be developed to target either ATXN8OS or the repeat expansion tracts within the regulatory regions of the ATXN8 or the ATXN8OS gene, or to correct the splicing defects of downstream effector genes such as Gabt4.
ncRNAs have also been reported to be dysregulated in Alzheimer’s disease (AD). For instance, miR-9 controls neuronal stem cell differentiation, is enriched within synapses, and is downregulated in AD. miR-9 appears to regulate the amyloid-β (Aβ) induction of the CAMKK2/AMPK pathway, and is itself controlled by Aβ42 (95). In primary neuronal cultures, miR-9 overexpression inhibited CAMKK2, attenuated Aβ42-induced synaptotoxicity, and regulated the hyperphosphorylation of tau proteins, which combine to form toxic intracellular aggregations. Therefore, ncRNAs are actionable targets for treating neurological disorders. However, a more robust panel of ncRNA targets to correct the phenotypes associated with AD without causing unexpected toxicity to normal brain or spinal function is needed. Once these candidates are identified, delivering ORNs across the blood-brain barrier will present another challenge. The antisense strategies originally used to target miRNAs in vivo, termed antagomiRs, are delivered to many tissues, with the notable exception of the brain (96). This suggests that certain chemical modifications of a single-stranded RNA are not sufficient for robust delivery and uptake into the CNS without an additional carrier. While certain delivery agents are being developed, companies including miRagen Therapeutics have an anti–miR-155 compound using LNA-based chemistries that may enable investigational new drugs for patients with ALS (97). Relying on newer chemically modified antisense ORNs may prove effective, given that modulation of certain miRNAs can promote tau phosphorylation in rat primary hippocampal neurons and impaired learning when injected directly into the hippocampal dentate gyrus in 3-month-old C57BL/6 WT mice (98).
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ncRNAs in cancer
Hanahan and Weinberg’s landmark review describes six molecular hallmarks that are shared among all cancer types (99). In particular, successful initiation of tumorigenesis requires that cells develop the ability to sustain proliferative signaling, evade growth suppressors, enable replicative immortality, resist cell death, induce angiogenesis, and activate invasion and metastasis. It is clear that ncRNAs are dysregulated in cancer and have been implicated in regulating fundamental tumorigenic processes (Table 3). This is explained by reciprocal or double-negative transcription factor–miRNA feedback loops that result in the fine-tuning of gene expression during normal cellular function (100–102). During tumorigenesis, these regulatory loops become disrupted. Similarly, lncRNAs such as MALAT-1, HOTAIR, and ANRIL are elevated in cancer while MEG3, lincRNA-p21, and PTENP1 appear to be downregulated (103). While the mechanisms by which lncRNAs contribute to cancer pathogenesis are still unclear, accumulating evidence suggests that lncRNAs regulate chromatin-modifying proteins such as PRC2 and coREST (104, 105). Given that hypermethylation of gene promoter regions occurs often in cancer, lncRNAs may harbor tumor-suppressive or oncogenic functions depending on how dysregulation of the respective lncRNA affects the activity of the aforementioned chromatin-modifying complexes.
Oncogenic ncRNAs can inhibit growth suppressors. For instance, a key regulator of CDKN1B is the miR-221/222 family of miRNAs, which are overexpressed in multiple cancer types. Targeting of CDKN1B by this miRNA family promotes enhanced cell cycle progression from G1 to S phase resulting in sustained proliferation (100). miR-Zip knockdown of miR-221 in an MDA-MB-231 triple-negative breast cancer mouse model inhibited tumor growth, confirming the pro-proliferative effect of miR-221 in vivo (101, 102). The targeting of another oncogenic miRNA, miR-155, is being pursued given that miR-155 supports lymphoma development in mouse models in the absence of Myc (50). miRagen Therapeutics has announced a phase I clinical trial for use of an unmodified LNA anti–miR-155 molecule, MRG-106, against cutaneous T cell lymphoma (CTCL). Since delivery of MRG-106 will be via direct injection into skin lesions, this compound’s delivery efficacy should be high, and it will be interesting to know how CTCL lesions respond to MRG-106 treatment.
Additionally, tumor-suppressive ncRNAs can target growth promoters. While numerous miRNAs are implicated in this process, recently, miR-34a has made headlines as the first miRNA mimic–based therapy to enter human clinical trials (ClinicalTrials.gov, NCT01829971). In preclinical models, systemic administration of miR-34a, packaged as a neutral lipid emulsion, either alone or in combination with let-7 (48, 49), reduced lung tumor volumes in KrasLSL-G12D p53loxP/loxP mice. The therapeutic effectiveness of tumor regression induced by miR-34a is unsurprising, given that miR-34a harbors strong tumor-suppressive properties across a broad spectrum of tumor types. A recent approach developed by the Asbestos Diseases Research Institute and EnGeneIC was instead used to re-express miR-16 in patients with malignant pleural mesothelioma and advanced non–small cell lung cancer (NSCLC) failing standard therapy (NCT02369198). These TargomiRs are hoped to deliver miR-16 in NSCLC as effectively as MRX34 in liver cancer. Interestingly, recent work indicates that the growth-suppressive effect of miR-16 is enhanced when it is coupled with miR-34a (105), highlighting the importance of combinatorial miRNA therapeutic approaches.
ncRNAs can also alter the senescent state of cancer cells. The miRNA regulation of sirtuins (e.g., miR-34a and SIRT1; ref. 47) is a classic example, given that sirtuins regulate the activity of gene products involved in cellular metabolism, inflammation, transcription, and cell survival. ncRNAs also regulate telomeric regions of chromosomes, which progressively shorten during cell division, eventually triggering senescence. Cancer cells circumvent this by expressing telomerase reverse transcriptase (TERT), which adds telomeric repeats to the 3′ end of chromosomes. The lncRNA TERRA is transcribed from the same locus and binds to telomerase, inhibiting its activity in vitro (106). Subsequently, tumor cells actively downregulate TERRA, extending the longevity of cancer cells through telomerase-mediated lengthening of chromosomal ends. An additional senescence-promoting ncRNA is GAS5, which induces downregulation of CDK6 in pancreatic, bladder, and gastric cancer and in some cases is anticorrelated with tumor size and advanced clinical stage (107, 108). Inhibition of GAS5 is associated with an increased frequency of cells in S phase, increased CDK6 protein levels, and altered p21/WAF1 levels, such that the incidence of cellular senescence is reduced (108). In an in vivo colorectal cancer model, tumors ectopically expressing GAS5 harbored significantly reduced tumor volumes and tumor burden, suggesting that targeting GAS5 is a potential therapeutic (109).
ncRNAs can also alter the cellular survival response to uncontrolled proliferation and DNA damage (110). miR-221/222 can abrogate programmed cell death in numerous cancers, and inhibition of these miRNAs increases apoptosis through activation of SIRT1 and/or downregulation of PUMA (111, 112). The oncogenic lncRNA ANRIL was also implicated in resistance to cell death. ANRIL was discovered by mapping of a germline deletion in a family with melanoma–neural system tumor syndrome. ANRIL functions by epigenetically silencing its target genes via recruitment of PRC2 to gene regions, including the P15 (also known as CDKN2B) gene loci (113). Therefore, under a normal physiological state, ANRIL functions as a balancer of p15 expression, and this homeostatic relationship becomes disrupted in cancer (114). siRNA studies in xenograft mouse models indicated that knockdown of ANRIL results in slower tumor growth and lower tumor weight than in controls (115). Overall, this suggests that ANRIL is a regulator of the key genetic networks controlling cell death in cancer, and could be a potential therapeutic target.
ncRNAs can also regulate neovascularization, a key feature of the tumorigenic process described by Judah Folkman nearly 5 decades ago (116). As tumors increase in size, associated capillary outgrowth occurs from the tumor to surrounding stroma and host blood vessels. This dependence on vessel formation for tumor growth indicated that tumor angiogenesis could be targeted therapeutically (117). ncRNAs play a role in tumor angiogenesis, given that miRNA-deficient tumors generated from Dicer KO mice are poorly vascularized and hypoxic (118, 119). Numerous miRNAs have been shown to modulate angiogenesis in mice (120–122). miR-7, for example, was delivered as a biodegradable polymeric nanoparticle to inhibit angiogenesis in a chick chorioallantoic membrane assay, as well as in a human glioblastoma xenograft model (123). A growing number of lncRNAs, such as HULC and HOXD-AS1, have also been identified as angiogenesis regulators (124). However, the lncRNA MEG3, part of the TP53 regulatory feedback loop, appears to play a more predominant role in angiogenesis (125). Enhanced expression of proangiogenic genes coincides with low MEG3 levels in human tumors, and in mice maternal deletion of Meg3 results in a significant increase in microvessel formation in the brain. These studies highlight the growing list of angiogenic factors that could serve as targets for cancer treatment.
While the molecular underpinning of metastasis has yet to be elucidated, it is clear that ncRNAs are fundamental regulators of this epithelial-to-mesenchymal transition (EMT). miR-21 is a classic example of an ncRNA that promotes the migration and invasion of cells in a broad range of cancers, primarily through downregulation of phosphatase and tensin homolog (PTEN) and programmed cell death protein 4 (PDCD4). Inhibition of miR-21 in chicken embryo metastasis assays is associated with less intravasation of colorectal tumor cells (126, 127). miR-21–mediated regulation of PTEN results in increased IL-6 signaling, subsequently inducing key characteristics of EMT, including PI3K activation and enhanced levels of phosphorylated STAT3 and NF-κB in HER2-positive breast cancer cells (128). In a different in vivo study using MDA-MB-231 breast cancer cells, delivery of anti–miR-10b in a nanoparticle formulation prevented lymph node metastasis (129). Additionally, a number of antimetastatic targets are regulated by miR-10b, including HOXD10, TBX5, and PTEN, and blocking miR-10b activity inhibits the expression of prometastatic factors such as RhoC (130, 131). Other groups have targeted the cell-extrinsic composition of the metastatic microenvironment. Le et al. found that extracellular vesicles derived from highly metastatic 4T1E breast cancer cells promoted the metastasis of weakly metastatic 4T07 cells in vivo (132). miR-200 was implicated in this process as a prometastatic factor despite the canonical role of the miR-200 family in suppressing EMT (133–135). Similarly, Zetter and colleagues found that metastatic cells from the lymph nodes of mice with prostate tumors exhibited an increasingly epithelial phenotype and an increased level of miR-200 (136). These studies raise the prospect of targeting exosomes to block tumor metastasis as a new and innovative therapeutic approach.
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