WO2013176477A1 - 세포 내 관통능을 가지는 rna 간섭을 유도하는 핵산 분자 및 그 용도 - Google Patents

세포 내 관통능을 가지는 rna 간섭을 유도하는 핵산 분자 및 그 용도 Download PDF

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WO2013176477A1
WO2013176477A1 PCT/KR2013/004463 KR2013004463W WO2013176477A1 WO 2013176477 A1 WO2013176477 A1 WO 2013176477A1 KR 2013004463 W KR2013004463 W KR 2013004463W WO 2013176477 A1 WO2013176477 A1 WO 2013176477A1
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Prior art keywords
nucleic acid
acid molecule
strand
lasirna
antisense
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Ceased
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PCT/KR2013/004463
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English (en)
French (fr)
Korean (ko)
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홍선우
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BMT Inc
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BMT Inc
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Priority to DK13794539.0T priority Critical patent/DK2853597T3/en
Priority to JP2015513901A priority patent/JP6139671B2/ja
Priority to EP13794539.0A priority patent/EP2853597B1/en
Priority to ES13794539T priority patent/ES2716818T3/es
Priority to EP18215244.7A priority patent/EP3514236A1/en
Priority to HK15112131.8A priority patent/HK1211319B/xx
Application filed by BMT Inc filed Critical BMT Inc
Priority to US14/403,121 priority patent/US10125362B2/en
Priority to CN201380038984.6A priority patent/CN104755620B/zh
Publication of WO2013176477A1 publication Critical patent/WO2013176477A1/ko
Anticipated expiration legal-status Critical
Priority to US16/135,766 priority patent/US10883105B2/en
Priority to US17/110,640 priority patent/US20210207137A1/en
Ceased legal-status Critical Current

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    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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Definitions

  • the present invention provides an RNAi comprising a first strand comprising a region complementary to a target nucleic acid and a second strand forming a complementary bond with the first strand.
  • a double-stranded nucleic acid molecule at least one nucleotide phosphate backbone contained in the nucleic acid molecule is substituted with phosphorothioate or phosphorodithioate and is a lipophilic compound.
  • a nucleic acid molecule for RNAi induction having a cell-penetrating ability, characterized in that) is coupled.
  • RNA small interfering RNA
  • dsRNA short double stranded RNA
  • 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 synergistic cleavage could be induced in the case of nucleic acid molecules in which ribozyme or DNAzyme were introduced into the single-stranded region of the first strand.
  • the nucleic acid molecule according to the invention shows a high gene suppression efficiency of more than 90% in the target site in vivo only by dissolving and injecting in a solution such as PBS without a separate carrier, the nucleic acid molecule according to the invention is formulated separately It could be confirmed that it is possible to develop a drug in the form of an injection without a process.
  • Example 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.
  • the present invention in another aspect, inhibits the gene expression containing the RNAi-derived nucleic acid molecule. It relates to a composition for.
  • the nucleic acid molecule may be included in the form of a nucleic acid complex to which the cell carrier is bound.
  • 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 target gene may be an endogenous gene or a transgene.
  • 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.
  • cp-lasiRNA (Survivin) -PS2 in which the PS2 modification was introduced at the same position in the cp-lasiRNA (Survivin) and the following cp-lasiRNA (Survivin) in the A549 cell line as in Example 1 or 2
  • real-time PCR was performed in the same manner as in Example 4 to measure the expression level of Survivin gene. The experiment was repeated twice, and the graph shows the mean and SD of the replicates.

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PCT/KR2013/004463 2012-05-22 2013-05-21 세포 내 관통능을 가지는 rna 간섭을 유도하는 핵산 분자 및 그 용도 Ceased WO2013176477A1 (ko)

Priority Applications (10)

Application Number Priority Date Filing Date Title
US14/403,121 US10125362B2 (en) 2012-05-22 2013-05-21 RNA-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor
JP2015513901A JP6139671B2 (ja) 2012-05-22 2013-05-21 細胞内貫通能を持ってｒｎａ干渉を誘導する核酸分子およびその用途
EP13794539.0A EP2853597B1 (en) 2012-05-22 2013-05-21 Rna-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor
ES13794539T ES2716818T3 (es) 2012-05-22 2013-05-21 Molécula de ácido nucleico inductora de interferencias de arn capaz de penetrar en las células y uso de la misma
EP18215244.7A EP3514236A1 (en) 2012-05-22 2013-05-21 Rna-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor
DK13794539.0T DK2853597T3 (en) 2012-05-22 2013-05-21 RNA INTERFERENCE-INducing NUCLEIC ACID MOLECULES WITH CELL PENETENING EQUIPMENT AND USE THEREOF
CN201380038984.6A CN104755620B (zh) 2012-05-22 2013-05-21 具有细胞内穿透能力的诱导rna干扰的核酸分子及其用途
HK15112131.8A HK1211319B (en) 2012-05-22 2013-05-21 Rna-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor
US16/135,766 US10883105B2 (en) 2012-05-22 2018-09-19 RNA-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor
US17/110,640 US20210207137A1 (en) 2012-05-22 2020-12-03 Rna-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR20120053950 2012-05-22
KR10-2012-0053950 2012-05-22

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US14/403,121 A-371-Of-International US10125362B2 (en) 2012-05-22 2013-05-21 RNA-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor
US16/135,766 Continuation US10883105B2 (en) 2012-05-22 2018-09-19 RNA-interference-inducing nucleic acid molecule able to penetrate into cells, and use therefor

Publications (1)

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WO2013176477A1 true WO2013176477A1 (ko) 2013-11-28

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PCT/KR2013/004463 Ceased WO2013176477A1 (ko) 2012-05-22 2013-05-21 세포 내 관통능을 가지는 rna 간섭을 유도하는 핵산 분자 및 그 용도

Country Status (8)

Country Link
US (3) US10125362B2 (https=)
EP (2) EP3514236A1 (https=)
JP (3) JP6139671B2 (https=)
KR (2) KR101567576B1 (https=)
CN (2) CN108148838A (https=)
DK (1) DK2853597T3 (https=)
ES (1) ES2716818T3 (https=)
WO (1) WO2013176477A1 (https=)

Cited By (6)

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Publication number Priority date Publication date Assignee Title
KR20180071362A (ko) * 2015-11-16 2018-06-27 올릭스 주식회사 MyD88 또는 TLR3을 타겟팅하는 RNA 복합체를 이용한 연령-관련 황반 변성의 치료
KR20180128423A (ko) * 2016-04-11 2018-12-03 올릭스 주식회사 연결 조직 성장 인자를 표적화하는 rna 복합체를 사용한 특발성 폐 섬유증의 치료 방법
KR20200098521A (ko) * 2017-11-13 2020-08-20 사일런스 테라퓨틱스 게엠베하 포스포로다이티오에이트 링키지를 포함하는 표적 유전자의 발현을 저해하기 위한 핵산
CN114174512A (zh) * 2019-05-20 2022-03-11 奥利克斯医药有限公司 抑制PD-1表达的不对称siRNA
RU2812806C2 (ru) * 2017-11-13 2024-02-02 Сайленс Терапьютикс Гмбх Нуклеиновые кислоты для ингибирования экспрессии гена-мишени, содержащие фосфодитиоатные связи
US12577354B2 (en) 2013-09-17 2026-03-17 Bolt Threads, Inc. Methods and compositions for synthesizing improved silk fibers

Families Citing this family (33)

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Publication number Priority date Publication date Assignee Title
DK2631291T3 (da) 2010-10-22 2019-06-11 Olix Pharmaceuticals Inc Nukleinsyremolekyler, der inducerer rna-interferens, og anvendelser deraf
CN108148838A (zh) 2012-05-22 2018-06-12 奥利克斯医药有限公司 具有细胞内穿透能力的诱导rna干扰的核酸分子及用途
KR102279110B1 (ko) * 2014-04-30 2021-07-20 올릭스 주식회사 LasiRNA를 유효성분으로 포함하는 피부 미백용 조성물
EP3277811B1 (en) 2015-04-03 2020-12-23 University of Massachusetts Fully stabilized asymmetric sirna
SMT202000454T1 (it) 2015-04-03 2020-11-10 Univ Massachusetts Cmposti oligonucleotidici per bersagliare l'mrn della huntingtina
CN111875265B (zh) 2015-05-15 2023-09-12 Ａｇｃ株式会社 化学增强玻璃
TW201718023A (zh) * 2015-08-06 2017-06-01 世代好公司 細胞滲透性蛋白質－抗體結合物及使用方法
US10633653B2 (en) 2015-08-14 2020-04-28 University Of Massachusetts Bioactive conjugates for oligonucleotide delivery
WO2017132669A1 (en) 2016-01-31 2017-08-03 University Of Massachusetts Branched oligonucleotides
CA3022877A1 (en) 2016-02-02 2017-08-10 Olix Pharmaceuticals, Inc. Treatment of angiogenesis-associated diseases using rna complexes that target angpt2 and pdgfb
KR102825946B1 (ko) 2016-02-02 2025-06-27 올릭스 주식회사 IL4Rα, TRPA1, 또는 F2RL1을 표적화하는 RNA 복합체를 사용한 아토피 피부염 및 천식의 치료
KR101916652B1 (ko) 2016-06-29 2018-11-08 올릭스 주식회사 작은 간섭 rna의 rna 간섭효과 증진용 화합물 및 이의 용도
CA3033368A1 (en) 2016-08-12 2018-02-15 University Of Massachusetts Conjugated oligonucleotides
US11591600B2 (en) 2017-02-10 2023-02-28 OliX Pharmaceuticals. Inc. Long double-stranded RNA for RNA interference
KR102321426B1 (ko) * 2017-02-21 2021-11-05 올릭스 주식회사 남성형 탈모 표적 유전자의 발현을 억제하는 비대칭 siRNA
JP7406793B2 (ja) 2017-06-23 2023-12-28 ユニバーシティー オブ マサチューセッツ ２テイル自己デリバリー型ｓｉＲＮＡおよび関連方法
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EP2853597A4 (en) 2016-01-27
JP2015518721A (ja) 2015-07-06
JP6139671B2 (ja) 2017-05-31
CN108148838A (zh) 2018-06-12
KR101581655B1 (ko) 2015-12-31
CN104755620B (zh) 2018-03-02
KR20130130653A (ko) 2013-12-02
DK2853597T3 (en) 2019-04-08
KR101581655B9 (ko) 2015-12-31
KR101567576B1 (ko) 2015-11-10
US20190002881A1 (en) 2019-01-03
US10125362B2 (en) 2018-11-13
US20210207137A1 (en) 2021-07-08
JP6629712B2 (ja) 2020-01-15
EP2853597B1 (en) 2018-12-26
CN104755620A (zh) 2015-07-01
US20150111948A1 (en) 2015-04-23
EP2853597A1 (en) 2015-04-01
KR20150118061A (ko) 2015-10-21

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