SMALL INTERFERENCE RNA COMPLEX WITH INCREASED INTRACELLULAR TRANSMISSION CAPACITY

Abstract

The present invention relates to a multi siRNA complex with increased intracellular transmission capacity and a multi-functional nucleic acid structure complex. The siRNA complex and multi-functional nucleic acid structure complex according to the invention have the advantage of having a novel structure that enables easier chemical synthesis compared to the existing shRNA system used to inhibit expression of a plurality of target genes and also enabling the inhibition of the expression of a plurality of genes at enhanced efficiencies compared to the existing siRNA. In addition, because it has high intracellular transmission capacity and also enables inhibition of the expression of target genes specifically without incurring non-specific antiviral reactions, it is very useful as the therapeutic agent mediated by the siRNA mechanism to treat cancer or viral infection. Furthermore, the multifunctional nuclei acid structure complex according to the invention can combine with functional nucleic acid oligonucleotides such as miRNA, antagomiR, antisense oligonucleotide, aptamer and ribozyme, in addition to siRNA, to provide diverse functionality.

Claims

1-35. (canceled)

36. A method of inhibiting gene expression, the method comprising: contacting a cell with a multi-functional siRNA structure for inhibiting gene expression of three target genes by RNA interference, the multi-functional siRNA structure comprising: a first siRNA for inhibiting expression of a first target gene; a second siRNA for inhibiting expression of a second target gene; and a third siRNA for inhibiting expression of a third target gene; wherein the first, second, and third siRNAs are formed from three RNA strands annealed together to form a Y-shaped structure having three double-stranded arms extending from a junction of the Y-shaped structure, and each of the first, second, and third siRNAs has an antisense strand having sequence complementarity to a sequence of a respective target gene and a sense strand having sequence complementarity to the sequence of the antisense strand.

37. The method of claim 36, wherein at least one of the first, second, and third siRNAs comprises a chemical modification.

38. The method of claim 37, wherein the chemical modification comprises a replacement of the 2 position of the ribose of at least one nucleotide of at least one of the three siRNAs by any one of a hydrogen atom, a fluorine atom, an O-alkyl group, an O-acyl group, and an amino group.

39. The method of claim 38, wherein the chemical modification comprises a 2-O-methyl (2-OMe) modification of at least three nucleotides of each of the three siRNAs in proximity to the junction of the Y-shaped structure.

40. The method of claim 36, wherein: the 3 end of the antisense strand of the first siRNA is joined to the 5 end of the sense strand of the second siRNA; the 3 end of the antisense strand of the second siRNA is joined to the 5 end of the sense strand of the third siRNA; and the 3 end of the antisense strand of the third siRNA is joined to the 5 end of the sense strand of the first siRNA.

41. The method of claim 36, wherein the siRNA structure further comprises a cationic delivery vehicle.

42. The method of claim 41, wherein the cationic delivery vehicle comprises polyethylenimine or a liposome.

43. The method of claim 36, wherein the method comprises inhibiting or treating a condition.

44. The method of claim 43, wherein the condition comprises cancer or a viral infection.

45. A method of inhibiting gene expression, the method comprising: contacting a cell with a multi-functional siRNA structure for inhibiting gene expression of three target genes by RNA interference, the multi-functional siRNA structure comprising: a first siRNA for inhibiting expression of a first target gene; a second siRNA for inhibiting expression of a second target gene; and a third siRNA for inhibiting expression of a third target gene; wherein the first, second, and third siRNAs are joined together via a linker moiety, and each of the first, second, and third siRNAs has an antisense strand having sequence complementarity to a sequence of a respective target gene and a sense strand having sequence complementarity to the sequence of the antisense strand.

46. The method of claim 45, wherein at least one of the first, second, and third siRNAs comprises a chemical modification.

47. The method of claim 46, wherein the chemical modification is a replacement of the 2 position of the ribose of at least one nucleotide of at least one of the three siRNAs by any one of a hydrogen atom, a fluorine atom, an O-alkyl group, an O-acyl group, and an amino group.

48. The method of claim 47, wherein the chemical modification comprises a 2-O-methyl (2-OMe) modification of at least three nucleotides of each of the three siRNAs in proximity to the linker moiety.

49. The method of claim 46, wherein: one of the antisense and sense strands of each of the first, second, and third siRNAs is directly coupled to the linker moiety and another one of the antisense and sense strands of each of the first, second, and third siRNAs is complementarily bound to the strand directly coupled to the linker moiety.

50. The method of claim 46, wherein the linker moiety is selected from the group consisting of a phosphoramidite compound, iodoacetyl compound, maleimide compound, epoxide compound, thiol-disulfide compound, thiolated Ellman's reagent, NHS or sulfo-NHS compound, and isocyanate compound.

51. The method of claim 50, wherein the linker moiety is a phosphoramidite compound.

52. The method of claim 46, wherein the siRNA structure further comprises a cationic delivery vehicle.

53. The method of claim 52, wherein the cationic delivery vehicle comprises polyethylenimine or a liposome.

54. The method of claim 46, wherein the method comprises inhibiting or treating a condition.

55. The method of claim 54, wherein the condition comprises cancer or a viral infection.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0034] FIG. 1 shows the structure of the tsiRNA (multiplex siRNA structure) of an siRNA complex according to the present invention (FIG. 1a) and is a set of graphs showing the gene silencing activity of the siRNA complex of the present invention (FIGS. 1b to 1d).

[0035] FIG. 2 is a set of graphs showing the gene silencing activity of a multiplex siRNA structure bound to PEI (FIG. 2a) or Lipofectamine 2000 (FIG. 2b) according to the present invention.

[0036] FIG. 3 is a set of fluorescence microphotographs of HeLa cells introduced with each of an FITC-labeled siRNA mixture (siLamin, siDBP, and FITC-siTIG3) bound to PEI and an FITC-labeled tsiRNA (FITC-tsiRNA) bound to PEI.

[0037] FIG. 4 shows the inventive multiplex siRNA structure (tsiRNA-CVA) targeting different regions of the CVA24 genome (FIG. 4a) and is a set of graphs showing a comparison of relative luciferase activities measured after three siRNA mixtures targeting said regions have been introduced into cells using PEI together with three respective luciferase vectors comprising different viral nucleotide sequences.

[0038] FIG. 5 shows the results of carrying out 5RACE analysis in order to confirm whether the siRNA structure according to the present invention inhibits gene expression by the same RNAi mechanism as that of 19+2 siRNA according to the prior art.

[0039] FIG. 6 is a graph showing a comparison between the levels of induction of interferon- (IFN-), measured by an RT-PCR after introducing an siRNA mixture and tsiRNA, which were each bound to PEI, in order to confirm whether the siRNA structure according to the present invention causes a nonspecific antiviral response.

[0040] FIG. 7 shows the structure of Trebler tsiSurvivin (T-tiSurvivin) used in the present invention.

[0041] FIG. 8 shows the nucleotide sequences of siSurvivin and long siSurvivin used as control groups for Trebler tsiSurvivin.

[0042] FIG. 9 is a set of graphs showing the gene silencing efficiency of a T-tiSurvivin-PEI delivery vehicle.

[0043] FIG. 10 shows a T-tiRNA structure prepared by binding siSurvivin, siIntegrin and si-catenin to Trebler phosphoramidite (FIG. 10a) and is a graph showing the gene silencing efficiency of the T-tiRNA structure (FIG. 10b).

[0044] FIG. 11 shows an MT-tiRNA structure prepared by binding Anti-miR21, siIntegrin and si-catenin to Trebler phosphoramidite (FIG. 11a) and is a set of graphs showing the gene silencing efficiency of the MT-tiRNA structure (FIG. 11b).

[0045] FIG. 12 is a graph showing a comparison of luciferase activities resulting from the introduction of T-tiAnti-miR21.

[0046] FIG. 13 shows the results of electrophoresis carried out to examine the rate of the isolation of a T-tiSurvivin caused by HS (FIG. 13a), a photograph showing the results of measuring intracellular delivery capacity using FITC (FIG. 13b), and a set of graphs showing fluorescence intensity using flow cytometry (FIGS. 13c and 13d).

[0047] FIG. 14 shows a graph showing the gene silencing efficiency of a T-tiSurvivin complex (FIG. 14a), a graph showing the inhibition of growth of HepG2 cells after introduction of the T-tiSurvivin complex (FIG. 14b), and a set of microscope images (FIG. 14c).

[0048] FIG. 15 is a set of graphs showing the levels of expression of IFITI mRNA (a), IFN-0 mRNA (b) and OAS2 mRNA in T98G cells transfected with a tiRNA complex.

[0049] FIG. 16 shows the results of electrophoresis of 27-bp dsRNA, siLamin, tsiRNA, siSurvivin and T-tiSurvivin before and after treatment with Dicer.

[0050] FIG. 17 shows a structure obtained by chemical modification of some nucleotides of tsiRNA.

[0051] FIG. 18 shows a structure obtained by chemical modification of some nucleotides of T-tiSurvivin.

[0052] FIG. 19 shows the results of electrophoresis of tsiRNA(OMe) (a) and T-tiSurvivin(OMe) (b), each having a chemical modification, after Dicer treatment.

[0053] FIG. 20 is a set of graphs showing the gene silencing efficiencies of tsiRNA(OMe) (a) and T-tiSurvivin(OMe) (b), each having a chemical modification.

BEST MODE FOR CARRYING OUT THE INVENTION

[0054] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art. Generally, the nomenclature used herein are well known and conventionally used in the art.

[0055] The definition of main terms used in the detailed description of the invention is as follows.

[0056] As used herein, the term siRNA (small interfering RNA) means a short double-stranded RNA (dsRNA) that mediates efficient gene silencing in a sequence-specific manner.

[0057] As used herein, the term gene is intended to have the broadest meaning, and the gene can encode a structural protein or a regulatory protein. Herein, the regulatory protein includes a transcriptional factor, a heat shock proteins, or a protein That is involved in DNA/RNA replication, transcription and/or translation. Also, the target gene whose expression is to be inhibited is resident in a viral genome which has integrated into the animal gene or may be present as an extrachromosomal element. For example, the target gene may be a gene on an HIV genome. In this case, the genetic construct is useful in inactivating translation of the HIV gene in a mammalian cell.

[0058] As used herein, the term complex of the multiplex siRNA or the multifunctional nucleic acid structure with the cationic cell delivery vehicle refers to a complex formed by a strong charge-charge interaction between the negative charge of the backbone of the multiplex siRNA and the positive charge of the cationic cell vehicle.

[0059] In one aspect, the present invention is directed to an siRNA complex having enhanced intracellular delivery capacity, in which a cationic cell delivery vehicle is bound to a multiplex siRNA structure comprising three or more siRNAs linked to each other at one end thereof.

[0060] As used herein, the term multiplex siRNA refers to an siRNA structure prepared in such a manner that three or more siRNAs are linked to each other at one end thereof. A plurality (e.g., four) of different siRNAs linked to each other may be used in the present invention, but it is preferable to use three different siRNAs linked to each other in order to inhibit the expression of a plurality of target genes while significantly increasing the intracellular delivery capacity thereof. Also, the multiplex siRNA preferably has a structure in which siRNAs are linked to each other at the 3end of the antisense strand in such a manner that the 5 end of the antisense strand faces the outside. FIG. 1a shows the multiplex siRNA of the present invention, obtained by linking siRNAs to each other, which target three different target genes.

[0061] The siRNAs may comprise a chemical modification. For example, the chemical modification may be one in which the hydroxyl group at the 2 position of the ribose of at least one nucleotide included in the siRNAs was replaced by any one of a hydrogen atom, a fluorine atom, an O-alkyl group, an O-acyl group and an amino group.

[0062] Also, in the present invention, the cationic cell delivery vehicle is a positively charged delivery reagent which is used to deliver nucleic acid (i.e., siRNA) into cells under in vitro or in vivo conditions. The cationic cell delivery vehicle strongly interacts with the multiplex siRNA structure of the present invention to form a complex so that the siRNAs can be effectively introduced into cells. The cationic cell delivery vehicle that is used in the present invention may be made of a cationic polymer or a cationic lipid. For example, liposomes such as polyethylenimine (PEI) or Lipofectamine 2000 (Invitrogen) may be used as the cell delivery vehicle, but it will be obvious to a person skilled in the art that any positively charged delivery reagent may be used to provide the complex of the present invention.

[0063] In another aspect, the present invention is also directed to a multifunctional nucleic acid structure in which one end of each of three or more nucleic acid oligonucleotides selected from the group consisting of siRNAs, miRNAs, antagomiRs, antisense oligonucleotides, ribozymes and aptamers is linked to a compound having three or more functional groups.

[0064] As used herein, the term multifunctional nucleic acid structure refers to a nucleic acid structure in which functional nucleic acid oligonucleotides such as siRNA, miRNA, antagomiR, an antisense oligonucleotide, ribozyme and an aptamer are bound to each functional group of a compound having three or more functional groups. As used herein, the term three or more nucleic acid oligonucleotides is intended to mean a structure either consisting of three or more nucleic acid oligonucleotides, or consisting of two or three identical nucleic acid oligonucleotides and one or more nucleic acid oligonucleotides different therefrom, or consisting of different nucleic acid nucleonucleotides. Specifically, as shown in FIGS. 7 and 10a, the structure may consist only of three or more siRNAs, or as shown in FIG. 11a, may consist of two siRNAs and one antagomiR.

[0065] These nucleic acid oligonucleotides may be prepared to comprise a chemical modification. For example, the chemical modification may be one in which the hydroxyl group at the 2 position of the ribose of at least one nucleotide included in the siRNA was replaced by any one of a hydrogen atom, a fluorine atom, an O-alkyl group, an O-acyl group and an amino group.

[0066] This multifunctional nucleic acid structure is prepared by binding one end of each of nucleic acid oligonucleotides, selected from the group consisting of siRNAs, miRNAs, antagomiRs, antisense, antisense oligonucleotides, ribozymes and aptamers, to a compound having three or more functional group. Specifically, it can be prepared by linking a nucleic acid fragment to each functional group of a compound having three or more functional groups, and then introducing a sequence, which can complementarily bind to the nucleic acid fragment, into the nucleic acid oligonucleotide so as to complementarily bind to the nucleic acid fragment.

[0067] Example of the compound having three or more functional groups, which is used in the present invention, include, but are not limited to, phosphoramidite compounds, iodoacetyl compounds, maleimide compounds, epoxide compounds, thiol-disulfide compounds, thiolated Ellman's reagent, NHS or sulfo-NHS compounds, isocyanate compounds and the like. It will be obvious to a person skilled in the art that any compound which can bind to three or more siRNAs or other functional nucleic acid oligonucleotides can be used without any particular limitation as the compound having three or more functional groups. Herein, the compound having three or more functional groups can be suitably linked with oligonucleotides having a terminal substituent such as amine or thiol.

[0068] For example, where a phosphoramidite compound is used as the linker, a novel multifunctional nucleic acid structure can be constructed by linking three nucleic acid fragments to a phosphoramidite compound having three arms, such as Trebler phosphoramidite (Trilink Bio Technology), constructing siRNAs whose sense or antisense strand comprises a sequence capable of complementarily binding to the nucleic acid fragments, and linking the constructed siRNAs to the nucleic acid fragments by complementary binding. As used herein, the term complementary binding means that some fragments which are included in the sense or antisense strand of siRNAs have a complementarity of about 70-80% or greater, preferably about 80-90% or greater, and more preferably about 90-95% or greater, and still more preferably about 95-99%, with the sequences of the nucleic acid fragments, or can completely complementarily hybridize with the sequence of the nucleic acid fragments. However, a mismatch can be intentionally introduced into a region for linkage at a level in which annealing is possible.

[0069] According to the present invention, a multifunctional nucleic acid structure complex can be provided by binding a cationic cell delivery vehicle to the multifunctional nucleic acid structure of the present invention by charge-charge interaction. Accordingly, in another aspect, the present invention relates to a multifunctional nucleic acid structure complex having enhanced intracellular delivery capacity, which comprises a cationic cell delivery vehicle bound thereto.

[0070] The cationic cell delivery vehicle that is used in the present invention may be made of a cationic polymer or a cationic lipid. For example, liposomes such as polyethylenimine (PEI) or Lipofectamine 2000 (Invitrogen) may be used as the cationic cell delivery vehicle, but it will be obvious to a person skilled in the art that any positively charged delivery reagent may be used to provide the complex of the present invention.

[0071] In one Example of the present invention, each of the siRNA complex according to the present invention and an siRNA-cationic lipid complex according to the prior art was introduced into cells, and the gene silencing efficiency of each structure was measured. As a result, it was found that the siRNA complex according to the present invention inhibited the expression of all the target genes in a more efficient manner than the conventional siRNA structure.

[0072] In addition, in the case of treating viral infection by the RNAi mechanism according to the prior art, viral escape caused by the substitution or deletion of nucleotides in the viral genome has become a problem. However, in another Example of the present invention, multiple siRNAs targeting three different regions of the viral genome were introduced into cells using PEI, and as a result, it was found that the multiplex siRNA structure significantly reduced the expression of mRNAs including the corresponding viral genome regions, suggesting that the present invention is also useful for the treatment of viral infection.

[0073] In still another Example of the present invention, the intracellular permeability of the siRNA complex was compared with conventional siRNAs using a fluorescence microscope. As a result, it was found that the siRNA complex according to the present invention had very excellent intracellular delivery capacity compared to the conventional siRNA structure bound to PEI. Specifically, the conventional siRNAs were reported to be unsuitable for binding to a cationic lipid such as polyethylenimine (PEI) and were found to have low intracellular permeability (FIG. 3), but it was found that the multiplex siRNA complex of the present invention did bind to a cationic cell delivery vehicle such as polyethylenimine (PEI), thereby exhibiting very high intracellular delivery capacity.

[0074] Accordingly, the present invention relates to a method of effectively delivering siRNA into cells, the method comprising a step of introducing the siRNA complex of the present invention into cells.

[0075] In addition, in still another Example of the present invention, the mechanism of the siRNA complex according to the present invention was compared with the conventional siRNA structure in order to confirm whether the siRNA complex of the present invention can be used in the same applications as those for general RNAi mechanisms. As a result, it was found that the multiplex siRNA structure of the siRNA complex according to the present invention inhibited gene expression by the same mechanism as that of the 19+2 siRNA structure of the prior art. This suggests that the siRNA complex according to the present invention can be used in the same applications as those for conventional RNAi.

[0076] Accordingly, intracellular delivery of the siRNA complex can efficiently inhibit the expression of target genes. Thus, in another aspect, the present invention relates to a composition for inhibiting gene expression containing an siRNA complex in which a cationic cell delivery complex is bound to a multiplex siRNA structure comprising three or more siRNAs linked to each other at one end thereof. Also, the present invention can provide a composition for inhibiting gene expression, which is in the form of a multifunctional nucleic acid structure complex comprising a cationic cell delivery vehicle bound to a multifunctional nucleic acid structure in which three or more siRNAs are linked with each other at one end thereof by a compound having three or more functional groups.

[0077] The multifunctional nucleic acid structure complex according to the present invention has a remarkable gene silencing effect, like the multiplex siRNA complex. Also, according to the present invention, the multifunctional nucleic acid structure may comprise, in addition to siRNAs, functional nucleic acid oligonucleotides, such as miRNA, antagomiR, an antisense oligonucleotide, an aptamer and ribozyme. Unlike multiple siRNAs that require a specific structure and the linkage of double-stranded RNAs such as siRNAs, a backbone structure having short oligonucleotides is constructed using a compound having three or more functional groups, whereby any nucleic acid oligonucleotide can be introduced into the structure. Thus, binding of single-stranded nucleic acid oligonucleotides such as antagomiR also becomes possible. In addition, because oligonucleotides are bound to the compound having three or more functional groups, a structure comprising nucleic acid fragments having a shorter length than multiple tsiRNAs can be provided, and thus the production cost of the structure is reduced and the preparation process thereof is also easily carried out.

[0078] In addition, in one Example of the present invention, whether the multifunctional nucleic acid structure complex and the multiplex siRNA complex according to the present invention induce immune responses was examined. As a result, it was found that the multiplex siRNA complex caused some nonspecific immune responses in T98G cells reported to have high immune sensitivity to dsRNA treatment, whereas the multifunctional nucleic acid structure complex did not cause such immune responses.

[0079] Also, in another Example of the present invention, resistance to Dicer was analyzed. As a result, it was found that the multifunctional nucleic acid structure complex showed higher resistance to Dicer.

[0080] Meanwhile, the composition for inhibiting gene expression according to the present invention may be provided in the form of a kit for inhibiting gene expression. The kit for inhibiting gene expression may take the form of bottles, tubs, sachets, envelops, tubes, ampoules, and the like, which may be formed in part or in whole from plastic, glass, paper, foil, wax, and the like. The container may be equipped with a fully or partially detachable lid that may initially be part of the container or may be affixed to the container by mechanical, adhesive, or other means. The container may also be equipped with a stopper, allowing access to the contents by a syringe needle. The kit may comprise an exterior package which may include instructions regarding the use of the components.

[0081] Also, the use of the composition for inhibiting gene expression can effectively inhibit the expression of two or more genes at the same time. Thus, in another aspect, the present invention relates to a method of inhibiting gene expression using the composition for inhibiting gene expression.

[0082] In addition, in another Example of the present invention, it was found that the complex according to the present invention had the effect of inhibiting the growth of cancer cells. Thus, in still another aspect, the present invention relates to an anticancer composition containing the multiplex siRNA complex or the multifunctional nucleic acid structure complex.

[0083] The anticancer composition of the present invention may be provided as a pharmaceutical composition comprising the complex alone or in combination with at least one pharmaceutically acceptable carrier, excipient or diuent. The complex may be contained in the pharmaceutical composition in a pharmaceutically effective amount according to a disease and the severity thereof, the patient's age, weight, health condition and sex, the route of administration and the period of treatment.

[0084] As used herein, the term pharmaceutically acceptable refers to a composition that is physiologically acceptable and does not cause gastric disorder, allergic reactions such as gastrointestinal disorder or vertigo, or similar reactions, when administered to humans. Examples of said carrier, excipient or diluent may include lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, polyvinylpyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate and mineral oils.

[0085] The pharmaceutical composition may additionally contain fillers, anti-aggregating agents, lubricants, wetting agents, perfumes, emulsifiers and preservatives. Also, the pharmaceutical composition of the present invention may be formulated using a method well known in the art, such that it can provide the rapid, sustained or delayed release of the active ingredient after administration to mammals. The formulation may be in the form of sterile injection solutions, etc.

EXAMPLES

[0086] Hereinafter, the present invention will be described in further detail with reference to examples. It will be obvious to a person having ordinary skill in the art that these examples are illustrative purposes only and are not to be construed to limit the scope of the present invention.

[0087] Particularly, Lamin A/C, DBP, TIG3, Survivin gene and a CVA24 viral genome were illustrated as target genes in the following Examples, but it will be obvious to a person skilled in the art that the inventive complex and composition that target other genes can show the same results as those in the Examples. Also, it will be obvious to a person skilled in the art that the use of functional nucleic acid oligonucleotides other than AntimiR-21 used in the following Examples can also provide the multifunctional nucleic acid structure of the present invention.

Example 1: Preparation of siRNA Complex According to the Present Invention

[0088] Multiple siRNAs used in Examples and siRNAs used in experiments were provided by purchasing chemically synthesized RNAs from Bioneer, Inc., and then annealing the RNAs according to the manufacturer's protocol.

[0089] First, a triple-target gene silencing siRNA (tsiRNA) targeting Lamin A/C, DBP and TIG3 mRNA were prepared as shown in FIG. 1a.

[0090] Three strands for providing the tsiRNA were as follows:

TABLE-US-00001 1.sup.ststrand: (SEQIDNO:1) 5-UGUUCUUCUGGAAGUCCAGUCGAAGACAUCGCUUCUCA-3 2.sup.ndstrand: (SEQIDNO:2) 5-UGAGAAGCGAUGUCUUCGACUGUCUCAGGCGUUCUCUA-3 3.sup.rdstrand: (SEQIDNO:3) 5-UAGAGAACGCCUGAGACAGCUGGACUUCCAGAAGAACA-3

[0091] Meanwhile, siRNAs for the three regions, used as control groups, were as follows:

TABLE-US-00002 siRNA(siLamin)forLaminmRNA sense: (SEQIDNO:4) 5-CUGGACUCCCAGAAGAACA(dTdT)-3 antisense: (SEQIDNO:5) 5-UGUUCUUCUGGAAGUCCAG(dTdT)-3 siRNA(siDBP)forDBPmRNA sense: (SEQIDNO:6) 5-UCGAAGACAUCGCUUCUCA(dTdT)-3 antisense: (SEQIDNO:7) 5-UGAGAAGCGAUGUCUUCGA(dTdT)-3 siRNA(siTIG3)forTIG3mRNA sense: (SEQIDNO:8) 5-CUGUCUCAGGCGUUCUCUA(dTdT)-3 antisense: (SEQIDNO:9) 5-UAGAGAACGCCUGAGACAG(dTdT)-3

[0092] To the tsiRNA obtained as described above, polyethylenimine (PEI; Polyplus) was added according to the manufacturer's protocol, thereby preparing an siRNA complex according to the present invention.

Example 2: Measurement of Gene Silencing Activities of siRNA Complex According to the Present Invention and siRNAs According to the Prior Art

[0093] Each of the complex of PEI with the triple-target gene silencing siRNA (tsiRNA) targeting A/C (Lamin A/C), DBP and TIG3 mRNA, prepared in Example 1, and a complex of PEI with each of siLamin, siDBP and siTIG3 that are the conventional siRNA structures described in Example 1, was introduced into HeLa cells (ATCC CCL-2). The HeLa cells were cultured in Dulbecco's modified Eagle's medium (Hyclone), supplemented with 10% FBS (fetal bovine serum), in a 12-well plate. Before introduction of each complex, the cells were cultured in antibiotic-free complete medium for 24 hours until a confluency of 80% was reached. The siRNA mixture was used at a concentration of 100 nM, and the tsiRNA was also used at a concentration of 100 nM. The PEI (N/P=5) used was purchased from Polyplus and introduced according to the manufacturer's protocol.

[0094] 3 hours after introduction of each complex, the medium was replaced with a fresh medium, and the levels of Lamin, DBP and TIG3 mRNA were measured by quantitative real-time RT-PCR. Specifically, total RNA was extracted from the cell lysate using a Tri-reagent kit (Ambion) and then used as a template for cDNA synthesis which was carried out using the ImProm-II reverse transcription system (Promega) according to the manufacturer's protocol. Then, the expression level of each of the target genes was measured using a step-one real-time PCR system (Applied Biosystems) according to the manufacturer's protocol, and the measured mRNA levels of Lamin, DBP and TIG3 were compared with the mRNA level of GAPDH (control group). Primers for each gene, used in the PCR amplification, were as follows:

TABLE-US-00003 PrimerpairforRT-PCRofDBP DBP-forward (SEQIDNO:10) 5-CCTCGAAGACATCGCTTCTC-3 DBP-reverse (SEQIDNO:11) 5-GCACCGATATCTGGTTCTCC-3 PrimerpairforRT-PCRofGAPDH GAPDH-forward (SEQIDNO:12) 5-GAGTCAACGGATTTGGTCGT-3 GAPDH-reverse (SEQIDNO:13) 5-GACAAGCTTCCCGTTCTCAG-3 PrimerpairforRT-PCRofLamin Lamin-forward (SEQIDNO:14) 5-CCGAGTCTGAAGAGGTGGTC-3 Lamin-reverse (SEQIDNO:15) 5-AGGTCACCCTCCTTCTTGGT-3 PrimerpairforRT-PCRofTIG3 TIG3-forward (SEQIDNO:16) 5-AGATTTTCCGCCTTGGCTAT-3 TIG3-reverse (SEQIDNO:17) 5-TTTCACCTCTGCACTGTTGC-3

[0095] After 30 minutes, 1 hour and 3 hours after introduction of each complex, the mRNA level of each of Lamin, DBP and TIG3 was measured. As a result, as shown in FIGS. 1b to 1d, the siRNA complex (tsiRNA) according to the present invention showed a more excellent gene silencing activity at all the time points.

[0096] Meanwhile, each of the siRNA complex (TsiRNA), obtained in Example 1, and an siRNA complex (TsiRNA-1) prepared by adding Lipofectamine 2000 (Invitrogen) to the siRNA complex (TsiRNA) of Example 1 according to the manufacturer's protocol, was introduced into HeLa cells (ATCC CCL-2) according to the same method as described above. 24 hours after introduction of each complex, the mRNA level of each gene was measured by RT-PCR.

[0097] As a result, as can be seen in FIG. 2, the mixture of each siRNA with PEI showed very limited gene silencing activity, similar to prior reports (Bolcato-Bellemin A. L. et al., Proc. Natl. Acad. Sci. U.S.A., 104:16050, 2007), but in the case of the TsiRNA bound to the cationic polymer PEI, and the TsiRNA bound to the cationic lipid Lipofectamine 2000, the mRNA levels of the three genes were significantly low.

[0098] Such results indicate that the siRNA complex according to the present invention is effective in inhibiting the expression of the three different genes, in comparison with the conventional siRNA structure bound to the cationic cell delivery vehicle such as PEI or Lipofectamine 2000.

Example 3: Measurement of Intracellular Delivery Capacity of siRNA Complex According to the Present Invention

[0099] In order to compare the intracellular delivery capacity between the siRNA complex of the present invention and the conventional siRNA (siTIG3), the following experiment was carried out.

[0100] The 3 end of the sense strand of siTIG3 and the 3 end of the TIG3 sense strand of tsiRNA were labeled with FITC. Also, each of the FITC-labeled siRNA mixture (siLamin, siDBP, and FITC-siTIG3) and the FITC-labeled tsiRNA (FITC-tsiRNA) was bound to PEI and introduced into HeLa cells. Then, the HeLa cells were observed with a fluorescence microscope (Olympus) at various time points.

[0101] The cells were observed 10 minutes, 30 minutes, 1 hour and 3 hours after introduction. As a result, as can be seen in FIG. 3, in the case in which the siRNA mixture was introduced using PEI (FIG. 3a), little or no fluorescence was observed at all the time points. However, in the case in which the FITC-labeled tsiRNA was introduced using PEI (FIG. 3b), green spots scattered in the intracellular regions could be observed, and the intensity of the spots was gradually increased as the culture time was increased.

[0102] Such results indicate that the siRNA complex according to the present invention has very high intracellular delivery capacity compared to the conventional siRNA structure bound to PEI.

Example 4: Targeting of Viral Genome

[0103] The inhibition of viral replication using the prior RNAi mechanism had a problem associated with a high rate of viral escape. In order to confirm whether this problem can be overcome and whether the siRNA structure according to the present invention is a general siRNA mechanism, the following experiments were carried out. For this purpose, the siRNA complex according to the present invention was prepared as shown in FIG. 4a (tsiRNA-CVA) so as to target three different regions (CRE, 3D1, and 3D2) of a viral genome (coxsackievirus A24; CVA24).

[0104] Three strands for providing the tsiRNA-CVA were as follows:

TABLE-US-00004 tsiRNA-CVA: 1.sup.ststrand: (SEQIDNO:18) 5-UCAAUACCGUGUUUGCUCUUGGUGAUGAUGUAAUUGCU-3 2.sup.ndstrand: (SEQIDNO:19) 5-AGCAAUUPCAUCAUCACCACCAUGACUCCAGCUGACAA-3 3.sup.rdstrand: (SEQIDNO:20) 5-UUGUCAGCUGGAGUCAUGGAGAGCAAACACCGUAUUGA-3

[0105] Meanwhile, siRNAs for the three regions, used as control groups, were as follows:

TABLE-US-00005 siRNA(siCVA-CRE)forCVA-CREmRNA sense: (SEQIDNO:21) 5-AGAGCAAACACCGUAUUGA(dTdT)-3 antisense: (SEQIDNO:22) 5-UCAAUACGGUGUUUGCUCU(dTdT)-3 siRNA(siCVA-3D1)forCVA-3D1mRNA sense: (SEQIDNO:23) 5-UGGUGAUGAUGUAAUUGCU(dTdT)-3 antisense: (SEQIDNO:24) 5-AGCAAUUACAUCAUCACCA(dTdT)-3 siRNA(siCVA-3D2)forCVA-3D2mRNA sense: (SEQIDNO:25) 5-CCAUGACUCCAGCUGACAA(dTdT)-3 antisense: (SEQIDNO:26) 5-UUGUCAGCUGGAGUCAUGG(dTdT)-3

[0106] Then, each of a target sequence for siCVA-CRE, a target sequence for siCVA-3D1 and a target sequence for siCVA-3D2 was inserted into the Spe II and HindIII positions of the 3 untranslated region of the luciferase mRNA-encoding gene of a pMIR Report-luciferase vector (Ambion), thereby constructing pMIR-CRE, pMIR-3D1 and pMIR-3D2 vectors. The inserted target sequences were as follows:

TABLE-US-00006 CREAS-target Hind (SEQIDNO:27) 5-AGCTTTCAATACGGTGTTTGCTCTA-3 Spe (SEQIDNO:28) 3-AAGTTATGCCACAAACGAGATGATC-5 3D1AS-target Hind (SEQIDNO:29) 5-AGCTTAGCAATTACATCATCACCAA-3 Spe (SEQIDNO:30) 3-ATCGTTAATGTAGTAGTGGTTGATC-5 3D2AS-target Hind (SEQIDNO:31) 5-AGCTTTTGTCAGCTGGAGTCATGGA-3 Spe (SEQIDNO:32) 3-AAACAGTCGACCTCAGTACCTGATC-5

[0107] Each of the vectors was introduced into the complex of siRNA mixtures (siCVA-CRE, siCVA-3D1, and siCVA-3D2) with PEI and the complex of tsiRNA-CVA with PEI, and then introduced into HeLa cells, after which the luciferase activity of the cells was measured. Specifically, 24 hours after introduction of each vector, the cells were lysed using the passive lysis buffer of a dual-luciferase reporter assay system (Promega). The luciferase activity was measured using a Victor3 plate reader (PerkinElmer) for firefly and Renilla luciferase.

[0108] As a result, as can be seen in FIG. 4b, the siRNA complex according to the present invention showed significantly low luciferase activity compared to the complex of the conventional art siRNA structure bound to PEI, like the results of Example 2.

[0109] Such experimental results indicate that the siRNA complex according to the present invention is also useful for inhibition of viral replication showing a high escape rate for prior RNAi mechanisms, suggesting that the structure of the siRNA complex according to the present invention is not limited only to the target gene silencing of Example 2, but can be provided as a general siRNA mechanism having improved intracellular delivery capacity and gene silencing efficiency.

[0110] In addition, in order to confirm whether the siRNA complex according to the present invention can be used in the same applications as those for the prior RNAi mechanism, the following experiment on the analysis of mechanism was carried out.

Example 5: Analysis of Gene Silencing Mechanism

[0111] In order to confirm whether the siRNA structure according to the present invention inhibits gene expression by the same RNAi mechanism as that of the conventional 19+2 siRNA, the following experiment was carried out. Specifically, to analyze the cleavage site of each target mRNA, 5RACE (Rapid amplification of cDNA ends) analysis was carried out.

[0112] First, the siRNA (siLamin, siDBP, and siTIG3) or the tsiRNA constructed in Example 1 was introduced into HeLa cells using PEI, and after 18 hours, total RNA was extracted from the cells using a Tri-reagent kit (Ambion). The total RNA (3 g) was ligated with 0.25 g of GeneRacer RNA oligo without pretreatment, and the GeneRacer RNA oligo-ligated total RNA was subjected to reverse transcription using GeneRacer oligo dT and a SuperScriptIII RT kit (Invitrogen). The RNA oligo-ligated mRNA was amplified using gene-specific primers. Next, the PCR product was cloned into a T&A vector (RBC), and then sequenced using an M13 forward primer.

TABLE-US-00007 TIG3Genespecific3 primer: (SEQIDNO:33) 5-GGGGCAGATGGCTGTTTATTGATCC-3 TIG3Genespecific3 nestedprimer: (SEQIDNO:34) 5-ACTTTTGCCAGCGAGAGAGGGAAAC-3 LaminGenespecific3 primer: (SEQIDNO:35) 5-CCAGTGAGTCCTCCAGGTCTCGAAG-3 LaminGenespecific3 nestedprimer: (SEQIDNO:36) 5-CCTGGCATTGTCCAGCTTGGCAGA-3 DBPgenespecificprimer (SEQIDNO:37) 5-CGGGACAGCACGGCGCGGTAGT-3 DBPgenespecific3 nestedprimer (SEQIDNO:38) 5-CTCCTGGCGCACGGCCACAACTT-3 M13forwardprimer (SEQIDNO:39) 5-GTTTTCCCAGTCACGAC-3

[0113] As a result, as can be seen in FIG. 5, in both the case of treatment with the siRNA-PEI complex and the case of treatment with the tsiRNA-PEI complex, Lamin, DBP and TIG3 mRNA were digested at the same position.

[0114] Such experimental results indicate that the multiplex siRNA structure of the siRNA complex according to the present invention inhibits gene expression by the same mechanism as that of the conventional 19+2 siRNA structure.

Example 6: Measurement of the Induction of Nonspecific Antiviral Responses

[0115] It was reported an RNA double strand having a length of 30 bp or more caused a nonspecific antiviral response in HeLa cells so that it did not cause specific gene silencing (Manche L. et al., Mol. Cell Biol., 12:5238, 1992; Elbashir S. M. et al., Nature, 411:494, 2001). Thus, whether the siRNA complex according to the present invention shows specific and efficient gene silencing when compared with the conventional siRNA structure was analyzed.

[0116] In order to confirm whether an antiviral response occurs, each of the siRNA mixture and tsiRNA of Example 2 was bound to PEI and introduced in cells, after which the level of induction of interferon- (IFN-) was measured by RT-PCR in the same manner as Example 2. A primer pair used in the RT-PCR was as follows, and poly (I:C)-introduced cells were used as a positive control group causing an antiviral response.

TABLE-US-00008 PrimerpairforRT-PCRofIFN- IFN- forward: (SEQIDNO:40) 5-AGAAGTCTGCACCTGAAAAGATATT-3 IFN- reverse: (SEQIDNO:41) 51-TGTACTCCTTGGCCTTCAGGTAA-3

[0117] As a result, as can be seen in FIG. 6, the siRNA complex according to the present invention showed less than 1% of the IFN- mRNA level induced by the positive control group (poly I:C), in the same manner as the case in which the siRNA mixture having the conventional siRNA structure was bonded to PEI and introduced in cells.

[0118] Such experimental results indicate that the multiplex siRNA structure of the siRNA complex according to the present invention shows no nonspecific antiviral response, like the conventional siRNA structure, even though it has a length of 30 bp or more.

Example 7: Preparation of Triplex siRNA Delivery Complex Using Linker and Measurement of Gene Silencing Activity Thereof

[0119] 7-1: Preparation of T-tiSurvivin and Measurement of Gene Silencing Activity Thereof

[0120] Using a triplex phosphoramidite compound (Trebler phosphoramidite, Trilink Bio Technology, USA) as shown in FIG. 7, a triplex siRNA delivery complex was constructed.

[0121] First, the Trebler phosphoramidite was purchased, and then three strands of a DNA oligonucleotide of SEQ ID NO: 42 was linked to the Trebler phosphoramidite by Genotech Co., Ltd., Korea (indicated by red; 5->3 direction from the Trebler). Then, an RNA oligonucleotide (SEQ ID NO: 43) having both a region having a nucleotide sequence complementary to the DNA oligonucleotide of SEQ ID NO: 42 and an siSurvivin antisense sequence, and an siSurvivin sense sequence (SEQ ID NO: 44) were annealed at the same time, thereby obtaining T-tiSurvivin as shown in FIG. 7. After that, each of the siSurvivin and long siSurvivin shown in FIG. 8 as a control group and the T-tiSurvivin shown in FIG. 7 was bound to PEI and delivered into HeLa cells, and 24 hours after delivery, the expression level of Survivin mRNA was measured by real-time RT-PCR in the same manner as Example 2. A primer pairs used in the RT-PCR was as follows:

TABLE-US-00009 Survivin-forward: (SEQIDNO:48) 5-GCACCACTTCCAGGGTTTAT-3 Survivin-reverse: (SEQIDNO:49) 5-CTCTGGTGCCACTTTCAAGA-3

[0122] As a result, as can be seen in FIG. 9a, the gene silencing effect of T-tiSurvivin was significantly increased compared to the conventional siRNA or long siSurvivin. Also, the IC.sub.50 value was measured. As a result, as can be seen in FIG. 9b, tiSurvivin showed an IC.sub.50 value which was about 11 times lower than that of the conventional siRNA structure. This suggests that the inventive triplex siRNA using the linker shows higher gene silencing efficiency than the conventional siRNA structure.

[0123] 7-2: Preparation of T-tiRNA Inhibiting the Expression of Survivin, Cateinin and Integrin and Measurement of Gene Silencing Activity Thereof

[0124] siSurvivin, siIntegrin and si-catenin were bound to Trebler phosphoramidite according to the same method as Example 7-1, thereby constructing a triplex siRNA delivery complex as shown in FIG. 10a. Then, each of a T-tiRNA of FIG. 10a and a mixture of siSurvivin, siIntegrin and si-catenin of FIG. 8 as a control group was bound to PEI and delivered into HeLa cells. 24 hours after intracellular delivery, the expression levels of Survivin mRNA, Integrin mRNA and -catenin mRNA were measured by real-time RT-PCR in the same manner as Example 2. Primer pairs used in the RT-PCR were as follows. Herein, the primer pair for Survivin was the same primer pair as used in Example 7-1.

TABLE-US-00010 Integrin-forward (SEQIDNO:54) 5-CGTATCTGCGGGATGAATCT-3 Integrin-reverse (SEQIDNO:55) 5-GGGTTGCAAGCCTGTTGTAT-3 -catenin-forward (SEQIDNO:56) 5-ATGTCCAGCGTTTGGCTGAA-3 -catenin-reverse (SEQIDNO:57) 5-TGGTCCTCGTCATTTAGCAG-3 siIntegrinsense: (SEQIDNO:58) 5-UGAACUGCACUUCAGAUAU(dTdT)-3 siIntegrinantisense: (SEQIDNO:59) 5-AUAUCUGAAGUGCAGUUCA(dTdT)-3 si-cateninsense: (SEQIDNO:60) 5-GUAGCUGAUAUUGAUGGACUU-3 si-cateninantisense: (SEQIDNO:61) 5-GUCCAUCAAUAUCAGCUACUU-3

[0125] As a result, as can be seen in FIG. 10b, the gene silencing effect of T-tiRNA was significantly increased compared to that of the siRNA mixture. This suggests that the inventive triplex siRNA structure using the linker has higher gene silencing efficiency than the conventional siRNA structure.

[0126] 7-3: Preparation of Multifunctional MT-tiRNA Inhibiting miR-21 and the Expression of Catenin and Integrin and Measurement of Gene Silencing Activity Thereof

[0127] Anti-miR21, siIntegrin and sip-catenin were bound to Trebler phosphoramidite in the same manner as Example 7-1, thereby constructing a triplex RNA structure as shown in FIG. 11a. Then, a target sequence for miR-21 was inserted into the SpeII and HindIII positions of the 3-untranslated region of the luciferase mRNA-encoding gene of a pMIR Report-luciferase vector (Ambion), thereby constructing a vector. The inserted target sequences were as follows:

TABLE-US-00011 miR-21target miR-21sense: (SEQIDNO:63) 5-AATGCACTAGTTCAACATCAGTCTGATAAGCTAGCTCAGCAAGCTTA ATGC-3 miR-21antisense: (SEQIDNO:64) 5-GCATTAAGCTTGCTGACTAGCTTATCAGACTGATGTTGAACTAGTGC ATT-3

[0128] With the vector, each of an MT-tiRNA of FIG. 11a and a mixture of Anti-miR21, siIntegrin and si-catenin as a control group was bound to PEI and delivered into HeLa cells, after which the luciferase activity of the cells was measured in the same manner as Example 4.

TABLE-US-00012 Anti-miR21: (SEQIDNO:65) 5-UCAACAUCAGUCUGAUAAGCUA-3

[0129] Also, each of an MT-tiRNA of FIG. 11a and a mixture of Anti-miR21, siIntegrin and si-catenin as a control group was bound to PEI and delivered into HeLa cells. 24 hours after intracellular delivery, the expression levels of Integrin mRNA and -catenin mRNA were measured by real-time RT PCR in the same manner as Example 2. The primer pair used in the RT-PCR was the same primer pair as used in Example 7-2.

[0130] As a result, as can be seen in FIG. 11b, the MT-tiRNA complex according to the present invention inhibited miR-21, suggesting that it has significantly increased luciferase activity. Namely, it could be seen that the nucleic acid structure complex according to the present invention was a multifunctional structure which could also exhibit a function of inhibiting miRNA.

[0131] Also, as can be seen in FIG. 11c, the gene silencing effect of T-tiRNA was significantly increased compared to that of the siRNA mixture. This suggests that the inventive triplex siRNA structure using the linker shows higher gene silencing efficiency than that of the conventional siRNA structure.

[0132] 7-4: Preparation of T-tiAnti-miR21 Inhibiting miR-21 and Measurement of miR-21 Inhibitory Activity Thereof

[0133] In addition, three Anti-miR21s were linked to Trebler phosphoramidite in the same manner as Example 7-1, thereby constructing a triplex RNA structure. Then, the luciferase activity thereof was measured in the same manner as Example 7-3. As a control group, Anti-miR21 was used.

[0134] As a result, as can be seen in FIG. 12, in the case in which T-tiAnti-miR21 was introduced, it inhibited miR-21, unlike the case in which the antagomiR Anti-miR21 was introduced, suggesting that the luciferase activity of T-tiAnti-miR21 was significantly increased. Namely, it could be seen that the nucleic acid structure complex according to the present invention inhibited the activity of miRNA at a higher efficiency than the conventional AntagomiR.

Example 8: Measurement of Binding Affinity for Cationic Cell Delivery Vehicle and Intracellular Delivery Capacity

[0135] 8-1: Comparison of Rate of Isolation Caused by HS

[0136] During a process of introducing nucleic acid into cells, the interaction between the nucleic acid and a cationic cell delivery vehicle can be inhibited due to a negatively charged proteoglycan present on the cell surface. Thus, the rate of isolation of the inventive multiplex siRNA complex by the cationic proteoglycan HS (heparan sulfate) that is expressed on the cell surface was analyzed in the following manner. For this purpose, each of the 19-bp siSurvivin of FIG. 8 and the T-tiSurvivin of FIG. 7 was bound to PEI (N/P=5), after which each complex and HS (Sigma/Aldrich) were incubated for 30 minutes while the amount of HS was gradually increased. Then, each of the incubated complexes was electrophoresed on 1% agarose gel, and the amount of siRNA released from each complex was measured. Herein, the measurement was carried out by staining with EtBr and visualization with UV transillumination.

[0137] As a result, as can be seen in FIG. 13a, siSurvivin was isolated from PEI by the same amount (1 equivalent (wt/wt)) of HS, whereas the complex according to the present invention was isolated only when it was incubated with a 4-fold-increased amount of HS. Such experimental results indicate that the multifunctional RNA structure complex according to the present invention has resistance to the influence of cationic cell surface substances before it is introduced into cells.

[0138] 8-2: Measurement of Intracellular Delivery Capacity Using FITC

[0139] In order to compare the intracellular delivery capacity between the multifunctional RNA structure (T-tiSurvivin) according to the present invention and the conventional siRNA structure (siSurvivin (FIG. 8)), each of the structures was labeled with FITC in the same manner as Example 3, and then observed with a fluorescence microscope.

[0140] As a result, as can be seen in FIG. 13b, siSurvivin was not substantially introduced into cells, but in the case of T-tiSurvivin according to the present invention, scattered green spots could be observed in intracellular regions.

[0141] In addition, the fluorescence intensity of the cells introduced with the FITC-labeled RNAs was measured using flow cytometry. The measurement was carried out by binding each of the FITC-labeled T-tiSurvivin and siSurvivin to PEI, transfecting each complex into HeLa cells, collecting the cells 3 hours after transfection, washing the collected cells twice with PBS, and then measuring the fluorescence intensity of the cells using an FACSCalibur system (Becton Dickinson).

[0142] As a result, as can be seen in FIG. 13c, the fluorescence intensity of the multifunctional nucleic acid structure according to the present invention was increased compared to the conventional siRNA structure. The fluorescence intensity was quantified and, as a result, as can be seen in FIG. 13d, the average fluorescence intensity was about 10 times different between the structures.

[0143] Such results indicate that the multifunctional nucleic acid structure according to the present invention has very excellent intracellular delivery properties compared to the conventional siRNA structure bound to PEI.

Example 9: Examination of Inhibitory Effect on Cancer Cell Growth

[0144] In order to examine whether the complex according to the present invention can be used in an anticancer composition, the expression level of Survivin mRNA was measured in the same manner as Example 7-1. As a result, it was found that T-tiSurvivin according to the present invention significantly inhibited the expression of Survivin in comparison with siSurvivin that is the conventional siRNA structure (FIG. 14a). Then, each of T-tiSurvivin of FIG. 7 and the siSurvivin of FIG. 8 was introduced into liver cancer HepG2 cells (ATCC No. HB-8065), and the degree of inhibition of growth of the cancer cells was measured.

[0145] As a result, as can be seen in FIGS. 14b and 14c, introduction of the inventive multifunctional RNA structure T-tiSurvivin bound to PEI showed the effects of inhibiting cancer cell growth and inducing apoptosis in the cancer cells, unlike introduction of siSurvivin and the untreated control group.

[0146] Specifically, it was found that the complex according to the present invention has the effect of inhibiting the growth of cancer cells, and thus can be provided as an anticancer composition for treating cancer and inhibiting cancer cell growth.

Example 10: Examination of Induction of Immune Response

[0147] In order to examine whether the multiplex siRNA structure and the nucleic acid structure according to the present invention induce an innate immune response mediated by dsRNA, whether the structures of the present invention express three antiviral immune response genes was examined in comparison with the conventional siRNA structure.

[0148] First, each of the T-tiSurvivin of FIG. 7, the siSurvivin of FIG. 8 and the siRNA mixture and tsiRNA of Example 2 was bound to Lipofectamine 2000 and introduced into T98G cells reported to have a very high immune sensitivity to dsRNA treatment, after which the levels of induction of IFIT1, IFN- and OAS2 were measured by an RT-PCR method in the same manner as Example 2. The primer pairs used in the RT-PCR were as follows, and poly (I:C)-introduced cells were used as a positive control group causing an antiviral response:

TABLE-US-00013 PrimerpairforRT-PCRofIFIT1 IFIT1-Forward (SEQIDNO:66) 5-GCCACAAAAAATCACAAGCCA-3 IFIT1-reverse (SEQIDNO:67) 5-CCATTGTCTGGATTTAAGCGG-3 PrimerpairforRT-PCRofIFN- IFN- forward: (SEQIDNO:40) 5-AGAACTCTGCACCTGAAAAGATATT-3 IFN- reverse: (SEQIDNO:41) 5-TGTACTCCTTGGCCTTCAGGTAA-3 PrimerpairforRT-PCRcfOAS2 OAS2-forward: (SEQIDNO:68) 5-TCAGAAGAGAAGCCAACGTGA-3 OAS2-reverse: (SEQIDNO:69) 5-CGGAGACAGCGAGGGTAAAT-3

[0149] As a result, as can be seen in FIG. 15, unlike the multifunctional nucleic acid structure complex according to the present invention, the multiplex siRNA complex according to the present invention induced the expression of IFIT1 and OAS2, known as viral immune response genes, in T98G cells reported to have a very high immune sensitivity to dsRNA treatment. Namely, it induced a nonspecific immune response. However, the multiplex siRNA complex according to the present invention showed less than 1% of the IFN- mRNA level induced by the positive control group (poly I:C), similar to Example 2 in which it was introduced into HeLa cells.

[0150] Such experimental results suggest that the multifunctional nucleic acid structure complex using a compound having three or more functional groups as a linker is more effective in avoiding the induction of a nonspecific immune response.

Example 11: Construction of Multiplex siRNA Complex and Multifunctional Nucleic Acid Structure Complex, Each Having Chemical Modification, and Examination of Whether the Complexes Act as Substrates for Dicer

[0151] It is known that, when long dsRNA is introduced into cells, it is digested by Dicer to produce 21-23-bp siRNAs. Thus, in order to examine whether the multiplex siRNA and multifunctional nucleic acid structures according to the present invention follow mechanisms different from the conventional dsRNAs, the following experiment was carried out.

[0152] 11-1: Examination of Whether tsiRNA and T-tiSurvivin Act as Substrates for Dicer

[0153] 30 pmol of each of a 27-bp dsRNA, the siLamin and tsiRNA of Example 2, the siSurvivin of FIG. 8 and the T-tiSurvivin of FIG. 7 was allowed to react using a Turbo Dicer siRNA generation Kit (Genlantis) for 12 hours according to the manufacturer's protocol, after which 2 l of a fraction of each reaction product was taken and developed on 10% non-denaturing polyacrylamide gel. The gel was stained with EtBr and visualized by UV transillumination.

TABLE-US-00014 27bpdsRNA Survivin27Sense: (SEQIDNO:70) 5-UCUUAGGAAAGGAGAUCAACAUUUUCA-3 Survivin27Antisense: (SEQIDNO:71) 5-UGAAAAUGUUGAUCUCCUUUCCUAAGA-3

[0154] As a result, as can be seen in FIG. 16, unlike the 27-bp dsRNA that was completely digested, the multiplex siRNA or multifunctional nucleic acid structure according to the present invention was not a good substrate for Dicer. However, tsiRNA was partially digested by Dicer. Thus, a multiplex siRNA structure and a multifunctional nucleic acid structure, each having a chemical modification, were constructed and subjected to the following experiments.

[0155] 11-2: Preparation of Multiplex siRNA Complex and Multifunctional Nucleic Acid. Structure, Each Having Chemical Modification, and Examination of Whether the Structures Act as Substrates for Dicer

[0156] A multiplex siRNA structure (tsiRNA(OMe)) and a multifunctional nucleic acid structure (T-tiSurvivin(OMe)), each having a chemical modification in which the hydroxyl group at the 2-position of the ribose of a nucleotide underlined by gray in one end of each of the tsiRNA of Example 2 and the T-tiSurvivin of FIG. 7 as shown in FIGS. 17 and 18 had been replaced by an O-methyl group, were prepared, and then subjected to the same experiment as described in Example 11-1.

[0157] As a result, as can be seen in FIG. 19, both tsiRNA(OMe) and T-tiSurvivin(OMe) did not act as substrates for Dicer.

[0158] 11-3: Examination of Gene Silencing Effects of Multiplex siRNA Complex and Multifunctional Nucleic Acid Structure Complex, Each Having Chemical Modification

[0159] In order to examine whether the multiplex siRNA complex and the multifunctional nucleic acid structure complex, which both had a chemical modification and did not act as substrates for Dicer as described in Example 11-2, have a gene silencing effect, RT-PCR was performed in the same manner as Example 2 and Example 7-1.

[0160] As a result, as can be seen in FIG. 20, both the multiplex siRNA complex and the multifunctional nucleic acid structure complex, each having a chemical modification, have excellent gene silencing effects.

INDUSTRIAL APPLICABILITY

[0161] As described above, the siRNA complex and the multifunctional nucleic acid structure complex according to the present invention have a novel structure which can be chemically synthesized in an easy manner for a conventional shRNA system for inhibiting the expression of a plurality of genes, while they can inhibit the expression of a plurality of genes at the same time at increased efficiency compared to the conventional siRNA. Also, they have high intracellular delivery capacity and can specifically inhibit the expression of target genes without causing a nonspecific antiviral response, and thus are highly useful as siRNA mechanism-mediated therapeutic agents for treating cancer or viral infection. In addition, the multifunctional nucleic acid structure complex can comprise, in addition to siRNAs, functional oligonucleotides, such as miRNA, antagomiR, an antisense oligonucleotide, an aptamer and ribozyme, and thus can perform various functions at the same time.

[0162] Although the present invention has been described in detail with reference to the specific features, it will be apparent to those skilled in the art that this description is only for a preferred embodiment and does not limit the scope of the present invention. Thus, the substantial scope of the present invention will be defined by the appended claims and equivalents thereof.