WO2012053741A2 - Rna 간섭을 유도하는 핵산 분자 및 그 용도 - Google Patents
Rna 간섭을 유도하는 핵산 분자 및 그 용도 Download PDFInfo
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Definitions
- the present invention relates to a nucleic acid molecule for inducing RNAi having a novel structure and a use thereof, and more particularly, a first strand having a length of 24 to 121 nt including a partial region complementary to a target nucleic acid, A nucleic acid molecule having a new structure which has a structure composed of a second strand of 13 to 21 nts having a region complementary to a region complementary to one strand of the target nucleic acid, thereby increasing the efficiency of inhibiting expression of the target gene; and It relates to a method for inhibiting the expression of the target gene using the same.
- RNA interference is a very specific and efficient mechanism for inhibiting gene expression, which is composed of a sense strand having a sequence homologous to an mRNA of a gene of interest and an antisense strand having a sequence complementary thereto.
- the double-stranded RNA (dsRNA) is introduced into cells to induce degradation of the target gene mRNA, thereby suppressing expression of the target gene.
- siRNAs used in the past are limited to 19-23 nucleotides (nt) in length of antisense strands. This is because the structure of the siRNA that researchers are using mimics the structure of long dsRNAs cut by Dicer in cells (Elbashir et al. Nature 2001, 411: 494-498). Early X-ray crystallography The results suggest a model in which the 5 'and 3' ends of the siRNA antisense strands introduced into Argonaute-2 (Ago2), a key component of the RISC complex, bind to the binding pockets of the Mid and PAZ domains, respectively (Song et. Nat. Struct. Biol.
- Ago2 Argonaute-2
- siRNA-DNA constructs have been reported that bind single-stranded DNA molecules that can act as primers for PCR for the detection of siRNAs in samples (US 2009/0012022 A1), which is only quantified. The addition of a tool to do this did not have a positive effect on the inhibition efficiency of the target gene.
- the present inventors have made efforts to provide a nucleic acid molecule that induces RNAi having a new structure with increased target gene suppression efficiency.
- the first strand having a length of 24 to 121 nt including some regions complementary to the target nucleic acid is shown.
- the long single strand region at the 3 'end of the first strand is provided.
- the nucleic acid oligonucleotides contained in the single stranded region of the 3 'end of the first strand may minimize the off-target, but may have an effect of targeting another target gene or inducing siRNA of the 5' end to the target gene. It was anticipated that the present invention was completed.
- An object of the present invention is to provide a nucleic acid molecule inducing RNAi of a novel structure with improved gene expression inhibitory effect.
- the present invention is complementary to the first strand of 24 ⁇ 121nt length comprising a partial region complementary to the target nucleic acid (target nucleic acid), and the partial region complementary to the target nucleic acid of the first strand
- a nucleic acid molecule that induces RNAi composed of a second strand of 13-21 nt in length having a region that forms an appropriate bond.
- the present invention also provides a nucleic acid complex in which a cell carrier is bound to the nucleic acid molecule inducing RNAi.
- the present invention also provides a method for intracellular delivery of a nucleic acid molecule inducing RNAi, wherein the nucleic acid complex is introduced into a cell.
- the present invention also provides a composition for inhibiting gene expression containing the nucleic acid molecule inducing the RNAi.
- the present invention also provides a kit for inhibiting gene expression containing the nucleic acid molecule inducing the RNAi.
- the present invention also provides a method for inhibiting gene expression comprising introducing the RNAi-derived nucleic acid molecule into a cell.
- the present invention also provides a method for inhibiting the expression of a target gene in a cell comprising the step of expressing the RNAi-derived nucleic acid molecule in a cell.
- the present invention also provides an anticancer composition containing the nucleic acid molecule inducing the RNAi.
- the present invention also provides a method for preventing or treating cancer, wherein the nucleic acid molecule for inducing RNAi is used.
- FIG. 1 is a schematic diagram of a nucleic acid molecule inducing RNAi according to the present invention.
- FIG. 2 shows a long-antisense siRNA (lsiRNA) in which the 3 'end of the antisense strand is elongated in a sequence complementary to the target mRNA.
- Figure 3 shows a long-antisense asiRNA (lasiRNA) of the 3 'end of the antisense strand of the asiRNA structure in a sequence complementary to the target mRNA.
- Figure 4 shows a long stretch of ribozyme or DNAzyme sequence targeting the target mRNA at the three ends of the antisense strand of the siRNA structure.
- 5 shows siRNA molecular structures that inhibit the expression of KRAS, a gene involved in cancer cell growth.
- Figure 6 is a graph showing the relative ratio of the KRAS mRNA level according to the introduction of the nucleic acid molecules of FIG.
- FIG. 7 is a graph showing the results of measuring KRAS mRNA expression levels according to the introduction of the nucleic acid molecules of FIG. 5 on the 1st, 2nd and 3rd days, respectively.
- FIG. 9 is a graph showing the relative ratio of KRAS mRNA levels according to the introduction of the nucleic acid molecules of FIG.
- Figure 10 is a graph showing the results of measuring the survival rate of the AGS cell line in accordance with the introduction of the nucleic acid molecules of Figure 8, respectively.
- FIG. 11 shows lsiRNA (21S + 10r) and lasiRNA (16S + 10r) with mRNA complementary expansion sequences and molecular structures (21S + 10rc, 16S + 10rc) with expansion sequences not complementary to mRNA for KRAS. Indicates.
- FIG. 12 is a graph showing relative ratios of KRAS mRNA levels according to the introduction of the nucleic acid molecules of FIG. 11.
- FIG. 14 is a graph showing the results of measuring the KRAS mRNA expression level according to the introduction of the nucleic acid molecules of FIG.
- FIG. 15 is a graph showing the results of measuring the survival rate of Hep3B cell line following the introduction of the nucleic acid molecules of FIG.
- FIG. 16 is a photograph showing the results of a 5 ′ RACE (Rapid amplification of cDNA ends) analysis.
- RNAi RNA interference
- dsRNA double-stranded RNA
- RNA small interfering RNA
- dsRNA short double stranded RNA
- an “antisense strand” is a polynucleotide that is substantially or 100% complementary to a target nucleic acid of interest, for example mRNA (messenger RNA), a non-mRNA RNA sequence (eg, microRNA, piwiRNA, tRNA, rRNA and hnRNA) or coding or non-coding DNA sequences may be complementary in whole or in part.
- mRNA messenger RNA
- non-mRNA RNA sequence eg, microRNA, piwiRNA, tRNA, rRNA and hnRNA
- antisense strands and guide strands can be used interchangeably.
- a "sense strand” is a polynucleotide having the same nucleic acid sequence as a nucleic acid of interest, and is characterized by mRNA (messenger RNA), non-mRNA RNA sequences (eg, microRNA, piwiRNA, tRNA, rRNA and hnRNA) or coding. Or a polynucleotide identical in whole or in part to a non-coding DNA sequence.
- mRNA messenger RNA
- non-mRNA RNA sequences eg, microRNA, piwiRNA, tRNA, rRNA and hnRNA
- the regulatory protein includes a transcription factor, a heat shock protein or a protein involved in DNA / RNA replication, transcription and / or translation.
- the gene of interest to be suppressed expression is inherent in the viral genome and may be integrated into an animal gene or exist as an extrachromosomal component.
- the gene of interest may be a gene on the HIV genome.
- siRNA molecules are useful for inactivating translation of HIV genes in mammalian cells.
- the present invention provides a complementary bond with a first strand having a length of 24 to 121 nt including a partial region complementary to a target nucleic acid, and a partial region complementary to the target nucleic acid of the first strand. It relates to a nucleic acid molecule that induces RNAi composed of a second strand of 13 ⁇ 21nt length having a region to (Fig. 1).
- the target nucleic acid is not limited thereto, but may be mRNA (messenger RNA), microRNA, piRNA (piwi-interacting RNA), coding DNA sequence, and non-coding DNA sequence.
- the length of the partial region complementary to the target nucleic acid (target nucleic acid) of the first strand may be characterized in that 19 ⁇ 21nt.
- the first strand comprises a single stranded region that does not bind to the second strand, preferably the first strand is a nucleic acid selected from the group consisting of antisense DNA, antisense RNA, ribozyme and DNAzyme in the single stranded region. It may be characterized in that it further comprises an oligonucleotide.
- a single stranded region which does not form a complementary bond with the second strand of the first strand may be connected to a region that forms a complementary bond with the second strand, either directly or by a linker, wherein the linker is It may be characterized as a chemical linker.
- the chemical linker is not limited thereto, but a nucleic acid (a nucleic acid moiety), PNA (a PNA moiety), peptide (a peptide moiety), a disulfide bond (a disulfide bond) or polyethylene glycol (a polyethylene glycol) moiety).
- the first strand may be characterized in that the single stranded region further contains a sequence complementary to the target nucleic acid or a sequence not complementary, in the case of complementary
- the double stranded region of the nucleic acid molecule according to the invention ie, the region complementary to the target nucleic acid of the siRNA, may be located continuously or may be located far away.
- the sequence targeted by siRNA and the sequence targeted by ribozyme or DNAzyme of the single-stranded region may be consecutively located or distantly located.
- the single-stranded region of the first strand has a sequence complementary to the target gene of the siRNA
- the sequence included in the single-stranded region is antisense DNA or antisense RNA
- the sequence of the sequence and the target gene of the siRNA is At least about 70-80%, preferably at least about 80-90%, even more preferably at least about 95-99%, complementary to each other, and if the single-stranded region is a ribozyme or DNAzyme
- the sequence of the gene of interest of siRNA may be characterized by complementary to at least about 50-60%.
- the single stranded region may be 5 to 100nt. If less than 5nt, the effect of increasing the gene expression inhibition efficiency is insignificant, and if more than 100nt, the synthesis efficiency of RNA molecules is reduced.
- the single-stranded region may be preferably 9 to 100nt, or may be characterized by having a length of 50nt or less, more preferably 10 to 15nt.
- At least one or more of the bases constituting the single-stranded region may be characterized as including a bulky base analog. If a large base analog, such as a deoxyadenosine derivative with a phenyl group, is included in the extension sequence, mRNA strands that complement the extension sequence will cleavage at the location of the large base analog. Any large base analogue that induces such cleavage can be included in the present invention without limitation.
- the 5 'end portion acts as an RNAi mechanism and the 3' end portion acts as an antisense mechanism or the 5 'terminal siRNA portion is targeted. It was predicted that it will act to induce mRNA. In this case, when the sequence complementary to the mRNA of the antisense 3 'end is DNA, RNase H-dependent mRNA cleavage may be induced.
- the bases constituting the single-stranded region of the antisense 3 'terminal contains a bulky base analog, or the single-stranded region is combined with mRNA to form a bulge structure It was predicted that cleavage could be induced. In addition, it was predicted that in the case of nucleic acid molecules in which ribozyme or DNAzyme was introduced into the single-stranded region of the first strand, synergistic cleavage could be induced.
- siRNA molecule consisting of a 19-21 nt long antisense strand and a 13-16 nt long sense strand, wherein the siRNA construct having the blunt end at the 5 'end of the antisense strand is an off-target effect by the sense strand of the siRNA.
- off-target effect means that siRNA is originally used to induce degradation of mRNA having a sequence complementary to an antisense strand and to obtain an effect of inhibiting gene expression of the mRNA.
- the unexpected degradation of other mRNAs generated by the sense strand or the inhibitory effect of expression of the corresponding gene and the antisense strand of the siRNA are paired with the wrong target. It is to include all the inhibitory effect of the degradation of the other mRNA by the antisense strand that occurs degradation of the expression of the gene.
- Nucleic acid molecules of the present invention may be synthesized in general, but are not limited thereto. That is, in the present invention, the nucleic acid molecule may be synthesized chemically or enzymatically.
- the siRNA molecules of the invention can be derived from naturally occurring genes by standard recombinant techniques, but in this case can be characterized as being substantially complementary at the nucleotide sequence level with at least a portion of the mRNA of the gene of interest to change expression.
- the nucleic acid molecule according to the present invention may be characterized by including chemical modification.
- the chemical modification is such that the hydroxyl group at the 2 'position of the ribose of at least one nucleotide contained in the nucleic acid molecule is substituted with any one of a hydrogen atom, a fluorine atom, an -O-alkyl group, an -O-acyl group, and an amino group.
- the phosphate backbone of at least one nucleotide may be substituted with any one of phosphorothioate form, phosphorodithioate form, alkylphosphonate form, phosphoroamidate form and boranophosphate form.
- the chemical modification may be characterized in that at least one nucleotide included in the nucleic acid molecule is substituted with any one of a locked nucleic acid (LNA), an unlocked nucleic acid (UNA), Morpholino, peptide nucleic acid (PNA).
- LNA locked nucleic acid
- UNA unlocked nucleic acid
- PNA Morpholino
- the chemical modification may be characterized in that the nucleic acid molecule is combined with at least one selected from the group consisting of lipids, cell penetrating peptides, and cell target ligands.
- nucleic acid molecule according to the present invention may be introduced into the cell by binding to the cell carrier, and thus the present invention relates to a nucleic acid complex in which the cell carrier is bound to the nucleic acid molecule inducing the RNAi.
- the cell carrier may be selected from the group consisting of cationic polymers, lipids, cell penetrating peptides and cell target ligands, and cationic polymers, such as cationic lipids.
- Sex carriers are used to deliver nucleic acids, ie siRNAs, into cells in either in vitro or in vivo, and are reagents for positively charged delivery.
- Cationic cell carriers interact strongly with the nucleic acid molecules of the present invention to form complexes so that nucleic acid molecules that induce RNAi can be efficiently introduced into the cell.
- Cationic polymers such as polyethyleneimine (PEI) or liposomes such as Lipofectamine 2000 (Invitrogen) can be used, but are not limited to these reagents for positively charged delivery and can be used to provide the complex according to the invention. Will be apparent to those of ordinary skill in the art.
- lipids such as cholesterol may be linked directly to nucleic acid molecules or indirectly by binding to other cell carriers and then to nucleic acid molecules.
- the embodiment of the present invention suggests that the RNAi-derived nucleic acid molecule according to the present invention has an effect of effectively inhibiting the expression of a target gene, and the present invention provides a gene containing the nucleic acid-derived nucleic acid molecule from another viewpoint. It relates to a composition for inhibiting expression.
- the nucleic acid molecule may be included in the form of a nucleus complex conjugated with a cell carrier.
- siRNAs targeting CTNNB1-2 can significantly increase the efficiency of inhibiting the expression of the target gene when applying the nucleic acid structure according to the present invention.
- the nucleic acid molecular structure according to the present invention can obtain the same result even when a nucleic acid molecule targeting other target genes is provided.
- kits for inhibiting gene expression may take the form of bottles, tubs, sachets, envelopes, tubes, ampoules, etc., which may be partially or wholly plastic, glass, paper, foil, It may be formed from a wax or the like.
- the container may be equipped with a fully or partially separable stopper, which may initially be part of the container or attached to the container by mechanical, adhesive, or other means.
- the container may also be equipped with a stopper, which may be accessible to the contents by a needle.
- the kit may include an external package, which may include instructions for use of the components.
- the present invention relates to a method of inhibiting expression of a target gene in a cell using the nucleic acid molecule inducing RNAi. That is, the present invention may provide a method for inhibiting expression of a target gene in a cell, comprising introducing the RNAi-derived nucleic acid molecule into a cell.
- the first strand of the nucleic acid molecule inducing RNAi may be characterized in that it is complementary to the mRNA sequence of the target gene.
- the target gene may be an endogenous gene or a transgene.
- the nucleic acid molecule according to the present invention is not necessarily limited to the synthetic siRNA, there is an advantage that can be applied to siRNA or shRNA that is expressed using an expression vector or the like in the cell. That is, the nucleic acid molecule according to the present invention can suppress the expression of the target gene by expressing it in a cell.
- the present invention relates to a method for inhibiting gene expression comprising expressing the RNAi-derived nucleic acid molecule in a cell.
- the RNAi-derived nucleic acid molecule according to the present invention may be a gene that causes or grows cancer by overexpression, that is, a tumor-related gene as a target gene, and thus may be usefully used as an anticancer composition.
- tumor-associated genes are not limited thereto, but KRas, Wnt-1, Hec1, Survivin, Livin, Bcl-2, XIAP, Mdm2, EGF, EGFR, VEGF, VEGFR, Mcl-1, IGF1R, Akt1, Grp78, It may be characterized in that any one of STAT3, STAT5a, ⁇ -catenin, WISP1 and c-myc.
- siRNA molecule of the structure according to the present invention by introducing the siRNA molecule of the structure according to the present invention into the cell inhibits the expression of KRAS, a gene involved in the growth of cancer cells, and by producing a siRNA molecule with beta-catenin as the target gene, Confirmed death.
- the anticancer composition according to the present invention includes a nucleic acid molecule for inducing the RNAi or a complex in which the nucleic acid molecule and the cell transporter are combined alone or as one or more pharmaceutically acceptable carriers, excipients or diluents.
- the complex may be included in the pharmaceutical composition in an appropriate pharmaceutically effective amount depending on the disease and its severity, the patient's age, weight, health condition, sex, route of administration and duration of treatment.
- pharmaceutically acceptable refers to a composition that is physiologically acceptable and that, when administered to a human, typically does not cause an allergic reaction such as gastrointestinal disorders, dizziness, or the like.
- carriers, excipients and diluents 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 oil.
- the pharmaceutical composition may further include fillers, anti-coagulants, lubricants, wetting agents, fragrances, emulsifiers and preservatives.
- Pharmaceutical compositions of the invention can also be formulated using methods known in the art to provide rapid, sustained or delayed release of the active ingredient after administration to a mammal.
- the formulations may be in the form of sterile injectable solutions and the like.
- RNAi-inducing nucleic acid molecule or the complex in which the nucleic acid molecule and the cell transporter are bound according to the present invention may further include a conventionally known anticancer chemotherapeutic agent, and thus a combination effect can be expected.
- cisplatin carboplatin, oxaliplatin, doxorubicin, dounorubicin, epirubicin, epirubicin, idarubicin, mitosantron (mitoxantrone), valubicin, curcumin, gefitinib, erlotinib, irinotecan, topotecan, topotecan, vinblastine, vincristine ( vincristine, docetaxel, paclitaxel and the like can be used.
- Example 1 Construction of long-antisense-guided siRNA: Preparation Example 1
- the length of the second strand is kept short at 21 nt, the region forming the double strand with the second strand is 19 nt, and the 3 'end of the first strand is a single strand of 17 nt in sequence complementary to the target mRNA. It was made to have an area.
- SiRNA having a long antisense strand was named as long-antisense siRNA (lsiRNA).
- the siRNA is induced into the target mRNA by the nucleic acid oligonucleotide included in the extension sequence or acts as a typical antisense mechanism (FIG. 2).
- SiRNA having a long antisense strand was named as long-antisense asiRNA (lasiRNA).
- the siRNA is induced into the target mRNA by the nucleic acid oligonucleotide included in the extension sequence or acts as a typical antisense mechanism (FIG. 3).
- CTNNB1-2siRNA and Dz339 DNAzyme were used to construct a structure having a long antisense strand such that the length of the sense strand was kept short at 21 nt and the DNAzyme at the 3 'end of the 19 nt long antisense strand.
- the constructed construct was named DNAzyme-guided siRNA (siRZNA) (FIG. 4).
- Example 4 lsiRNA production and KRAS gene expression inhibition inhibiting the expression of KRAS gene expression
- SiRNA was designed to inhibit the expression of KRAS, a gene involved in the growth of cancer cells.
- a long antisense siRNA (lsiRNA) was added to each of the 5 ', 10, and 15 nt of the antisense strand of the existing siRNA structure (19 + 2).
- the structure expanded with DNA of a sequence complementary to the target mRNA 21S + 5d, 10d, 15d
- the structure expanded with DNA of a sequence not complementary to the target mRNA as a control 21S + 5c, 10c, 15c)
- Fig. 5 target gene expression inhibition efficiency
- a structure (21 + 15d-mut) mutated the seed sequence of lsiRNA was constructed to test whether the gene inhibition of lsiRNA was dependent on seed sequence like siRNA.
- Each siRNA and lsiRNA were transfected into AGS cells (ATCC CRL 1739, Gastric adenocarcinoma, human) using lipofectamine2000 (invitrogen) at a concentration of 10 nM.
- Primers used in real-time PCR for mRNA measurement are as follows.
- the lsiRNA having a single-stranded region complementary to the target mRNA showed improved target gene suppression ability compared to the existing siRNA structure, this trend is proportional to the length of the single-stranded region could know.
- lsiRNA control with a single stranded region not complementary to the target mRNA could not observe this enhanced gene expression inhibition. Such enhanced gene expression inhibition could not be observed.
- lsiRNA having a seed sequence mutation it was confirmed that the target gene suppression almost disappeared. This shows that lsiRNA inhibits the target gene by seed sequence-dependent RNAi mechanism like the existing siRNA, and nonspecific gene suppression due to the modified structure does not occur.
- lsiRNA better maintains target gene suppression after introduction into cells compared to siRNA.
- the inhibition of gene expression reached the highest after 1 day of cell introduction, and it was confirmed that the inhibition decreased as the 2nd and 3rd days were reached (FIG. 7).
- lsiRNA was found to maintain the target gene expression inhibition until 3 days after introduction into the cell.
- lsiRNA control with a single stranded region not complementary to the target mRNA could not observe this enhanced gene expression inhibition. This result shows that the lsiRNA having a single stranded region complementary to the mRNA of the target gene not only shows higher efficiency of gene expression inhibition compared to the existing siRNA structure, but also maintains its efficacy longer.
- Example 5 lasiRNA production and KRAS gene expression inhibition to inhibit KRAS gene expression confirmed
- Example 4 it was investigated whether the nucleic acid molecular structure according to the present invention can improve its target gene expression inhibition when applied to asymmetric shorter duplex siRNA (asiRNA).
- siRNA asymmetric shorter duplex siRNA
- Example 4 a structure (16S + 5d, 10d, 15d) extended to DNA having a sequence complementary to the target mRNA at the 3 'end of the antisense strand of the conventional asiRNA structure and a control extended to DNA of a non-complementary sequence ( 16S + 5c, 10c, 15c) long antisense asiRNA (lasiRNA) was prepared and transfected into AGS cells to compare cancer cell growth inhibition (FIG. 8). After transfecting these RNAs into AGS cells, real-time PCR was performed in the same manner as in Example 4 to verify KRAS expression inhibitory efficiency as a target gene (FIG. 9). Each asiRNA and lasiRNA were transfected into AGS cells (ATCC CRL 1739, Gastric adenocarcinoma, human) using lipofectamine2000 (invitrogen) at a concentration of 10 nM.
- AGS cells ATCC CRL 1739, Gastric adenocarcinoma, human
- lasiRNA having a single-stranded extension sequence complementary to the target mRNA was confirmed to increase the target mRNA inhibitory capacity in proportion to the length of the extension sequence.
- this effect was not observed when the extension sequence was not complementary to the target mRNA.
- Example 6 Confirmation of growth inhibition of AGS cancer cell by lasiRNA and lasiRNA that inhibit KRAS gene expression
- KRAS mRNA expression inhibitory ability and cancer cell growth inhibitory ability had a high correlation. That is, it was confirmed that lsiRNA (21S + 15d) having 15 expansion sequences compared to siRNA showed more potent cancer cell growth inhibitory activity, and also increased cancer cell growth inhibitory activity of lasiRNA (16S + 15d) compared to asiRNA (FIG. 10). ). On the other hand, the lsiRNA introduced a mutation in the seed sequence (LASmut) was confirmed that the induction of cancer cell growth inhibition did not show nonspecific cytotoxicity due to the long expansion sequence structure. These results show that by introducing a single stranded region complementary to the target mRNA at the antisense strand 3′-end of siRNA and asiRNA, it is possible to increase gene suppression and thus intracellular phenotype expression.
- Example 7 Confirmation of KRAS gene expression inhibition by lsiRNA and lasiRNA whose expansion sequences are RNA
- lsiRNA (21S + 10r) and lasiRNA (16S + 10r) having 10 mRNA complementary expansion sequences were prepared, and structures having expansion sequences not complementary to mRNA as controls (21S + 10rc, 16S + 10rc). ) was also produced.
- KRAS mRNA expression inhibition efficiency was examined in the same manner as in Example 4.
- Example 8 lasiRNA production inhibiting CTNNB1 gene expression and CTNNB1 gene expression inhibition
- a lasiRNA structure corresponding to asiRNA targeting beta-catenin was prepared to confirm whether the nucleic acid molecular structure according to the present invention can induce an increase in the activity of asiRNA targeting other genes (FIG. 13). Then, Hep3B cells (ATCC HB 8064) were transfected with lipofectamine 2000 at a concentration of 10 nM, and then the expression inhibition of the gene of interest was examined by real-time PCR.
- Increasing target gene inhibition by this lasiRNA structure was again verified by measuring Hep3B cancer cell growth inhibition. That is, 5 days after the introduction of 10 nM siRNA, asiRNA, lasiRNA into Hep3B cells, the degree of cell growth was examined by measuring the number of cells. Cell viability was investigated by directly measuring the number of cells through microscopic observation. Briefly, 10 nM of siRNA, asiRNA and lasiRNA were transfected into AGS cells seeded in 96 well plates, and the number of surviving cells after 5 days was directly counted and measured.
- siRNA cancer cell killing ability was slightly reduced compared to siRNA, but lasiRNA having a complementary expansion target gene showed a similar level of cell killing power as siRNA. It was confirmed that lasiRNA with non-complementary expansion sequences did not increase cell killing ability as compared with asiRNA. This indicates that siRNA molecules having an extension sequence containing a sequence complementary to the target gene at the 3 'end of the antisense strand have increased target gene expression inhibitory ability.
- RNA oligo-ligated mRNA was amplified using gene specific primers. PCR products were then cloned into T & A vector (RBC) and sequenced with M13 forward primer.
- the nucleic acid molecular structure according to the present invention targets siRNAs by targeting a target gene complementary to some regions of the first strand according to the nucleic acid oligonucleotide included in the single strand region of the 3 'end of the first strand.
- siRNAs by targeting a target gene complementary to some regions of the first strand according to the nucleic acid oligonucleotide included in the single strand region of the 3 'end of the first strand.
- the use of the nucleic acid molecule according to the present invention can extend the duration of gene suppression efficiency.
- the RNAi-derived nucleic acid molecule according to the present invention is useful because it can be used in the treatment of cancer or virus infection using siRNA by replacing the conventional siRNA molecules.
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Abstract
Description
Claims (30)
- 목적 핵산(target nucleic acid)과 상보적인 일부 영역을 포함하는 24~121nt 길이의 제1가닥과, 상기 제1가닥의 목적 핵산과 상보적인 일부 영역과 상보적 결합을 형성하는 영역을 갖는 13~21nt 길이의 제2가닥으로 구성되는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥은 5' 말단에 1 내지 3nt의 돌출부를 가지는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제2가닥은 3' 말단에 1 내지 3nt의 돌출부를 가지는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥의 5' 방향의 말단이 블런트 말단(blunt end)인 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제4항에 있어서, 상기 제1가닥과 결합하는 제2가닥의 길이는 13~16nt인 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥의 목적 핵산(target nucleic acid)과 상보적인 일부 영역의 길이는 19~21nt 인 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 목적 핵산은 mRNA (messenger RNA), microRNA, piRNA (piwi-interacting RNA), 코딩 DNA 서열 및 비코딩 DNA 서열 중 어느 하나인 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥 중 제2가닥과 상보적 결합을 형성하지 않는 단일 가닥 영역은, 링커에 의하여 상기 제2가닥과 상보적 결합을 형성하는 영역에 연결되는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제8항에 있어서, 상기 링커는 화학적 링커(chemical linker)임을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제9항에 있어서, 상기 화학적 링커는 핵산 (a nucleic acid moiety), PNA (a PNA moiety), 펩타이드 (a peptide moiety), 다이설퍼이드 결합 (a disulfide bond) 또는 폴리에틸렌 글리콜 (a polyethylene glycol moiety)인 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥은 단일 가닥 영역에 상기 목적 핵산과 상보적인 서열을 추가로 함유하는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥은 단일 가닥 영역에 안티센스 DNA, 안티센스 RNA, 라이보자임 및 DNAzyme으로 구성된 군에서 선택되는 핵산올리고뉴클레오티드를 추가로 포함하는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 화학적 변형을 포함하는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제13항에 있어서, 상기 화학적 변형은 상기 핵산 분자에 포함되는 적어도 1종의 뉴클레오티드의 리보스의 2' 위치의 히드록실기가 수소원자, 불소원자, -O-알킬기, -O-아실기 및 아미노기 중 어느 하나로 치환된 것임을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제13항에 있어서, 상기 화학적 변형은 상기 핵산 분자에 포함되는 적어도 1종의 뉴클레오티드의 포스페이트 백본이 phosphorothioate form, phosphorodithioate form, alkylphosphonate form, phosphoroamidate form 및 boranophosphate form 중 어느 하나로 치환된 것임을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제13항에 있어서, 상기 화학적 변형은 상기 핵산 분자에 포함되는 적어도 1종의 뉴클레오티드가 LNA (locked nucleic acid), UNA(unlocked nucleic acid), Morpholino 및 PNA (peptide nucleic acid) 중 어느 하나로 치환된 것임을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제13항에 있어서, 상기 화학적 변형은 상기 핵산 분자가 지질, 세포투과성 펩타이드(cell penetrating peptide) 및 세포 표적 리간드로 구성된 군에서 선택되는 하나 이상과 결합된 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항에 있어서, 상기 제1가닥에서 단일 가닥 영역을 구성하는 염기 중 적어도 하나 이상이 거대한(bulky) 염기 유사체(base analog)를 포함하는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자.
- 제1항 내지 제18항 중 어느 한 항의 RNAi를 유도하는 핵산 분자에 세포전달체가 결합되어 있는 핵산 복합체.
- 제19항에 있어서, 상기 세포전달체는 양이온성 폴리머, 지질, 세포투과성 펩타이드(cell penetrating peptide) 및 세포 표적 리간드로 구성된 군에서 선택되는 것을 특징으로 하는 핵산 복합체.
- 제19항의 핵산 복합체를 세포 내로 도입시키는 것을 특징으로 하는 RNAi를 유도하는 핵산 분자의 세포 내 전달방법.
- 제1항 내지 제18항 중 어느 한 항의 RNAi를 유도하는 핵산 분자를 함유하는 유전자 발현 억제용 조성물.
- 제22항에 있어서, 상기 핵산 분자에 세포전달체를 추가로 결합시킨 것을 특징으로 하는 유전자 발현 억제용 조성물.
- 제1항 내지 제18항 중 어느 한 항의 RNAi를 유도하는 핵산 분자를 세포 내 도입시키는 단계를 포함하는 세포 내 목적 유전자의 발현 억제 방법.
- 제24항에 있어서, 상기 핵산 분자에 세포전달체를 추가로 결합시킨 것을 특징으로 하는 세포 내 목적 유전자의 발현 억제 방법.
- 제1항 내지 제18항 중 어느 한 항의 RNAi를 유도하는 핵산 분자를 세포 내에서 발현시키는 단계를 포함하는 세포 내 목적 유전자의 발현 억제 방법.
- 제1항 내지 제18항 중 어느 한 항의 구조를 가지는 RNAi를 유도하는 핵산 분자를 함유하는 항암 조성물.
- 제27항에 있어서, 상기 핵산 분자에 세포전달체를 추가로 결합시킨 것을 특징으로 하는 항암 조성물.
- 제27항에 있어서, 상기 핵산 분자는 종양 관련 유전자를 목적유전자로 하는 것을 특징으로 하는 항암 조성물.
- 제29항에 있어서, 상기 종양 관련 유전자는 KRAS, Wnt-1, Hec1, Survivin, Livin, Bcl-2, XIAP, Mdm2, EGF, EGFR, VEGF, VEGFR, Mcl-1, IGF1R, Akt1, Grp78, STAT3, STAT5a, β-catenin, WISP1 및 c-myc 중 어느 하나인 것을 특징으로 하는 항암 조성물.
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CN103328633B (zh) | 2018-07-10 |
CA2818662A1 (en) | 2012-04-26 |
US10214744B2 (en) | 2019-02-26 |
ES2732929T3 (es) | 2019-11-26 |
EP2631291B1 (en) | 2019-05-15 |
EP3599280A1 (en) | 2020-01-29 |
CA2818662C (en) | 2021-07-06 |
CN103328633A (zh) | 2013-09-25 |
EP2631291A4 (en) | 2015-01-14 |
DK2631291T3 (da) | 2019-06-11 |
US9637742B2 (en) | 2017-05-02 |
US20130273657A1 (en) | 2013-10-17 |
KR20120042645A (ko) | 2012-05-03 |
WO2012053741A9 (ko) | 2012-08-02 |
EP3599280B1 (en) | 2022-11-02 |
EP2631291A2 (en) | 2013-08-28 |
JP2013544505A (ja) | 2013-12-19 |
ES2930555T3 (es) | 2022-12-16 |
KR101328568B1 (ko) | 2013-11-13 |
JP5795072B2 (ja) | 2015-10-14 |
US20190177732A1 (en) | 2019-06-13 |
WO2012053741A3 (ko) | 2012-06-14 |
US10829760B2 (en) | 2020-11-10 |
US20170335326A1 (en) | 2017-11-23 |
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