WO2012029986A1 - アンチセンス核酸 - Google Patents

アンチセンス核酸 Download PDF

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Publication number
WO2012029986A1
WO2012029986A1 PCT/JP2011/070318 JP2011070318W WO2012029986A1 WO 2012029986 A1 WO2012029986 A1 WO 2012029986A1 JP 2011070318 W JP2011070318 W JP 2011070318W WO 2012029986 A1 WO2012029986 A1 WO 2012029986A1
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Prior art keywords
nucleic acid
exon
synthetic nucleic
antisense oligomer
seq
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English (en)
French (fr)
Japanese (ja)
Inventor
渡辺直樹
佐藤洋平
武田伸一
永田哲也
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Nippon Shinyaku Co Ltd
National Center of Neurology and Psychiatry
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Nippon Shinyaku Co Ltd
National Center of Neurology and Psychiatry
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Priority to EP11821996.3A priority Critical patent/EP2612917B1/en
Priority to SI201130767A priority patent/SI2612917T1/sl
Priority to PL11821996T priority patent/PL2612917T3/pl
Priority to US13/819,520 priority patent/US9079934B2/en
Priority to HRP20160336TT priority patent/HRP20160336T1/hr
Priority to JP2012531987A priority patent/JP5363655B2/ja
Priority to RU2013114396A priority patent/RU2567664C3/ru
Priority to CA2809637A priority patent/CA2809637C/en
Priority to DK11821996.3T priority patent/DK2612917T3/en
Priority to EP24168426.5A priority patent/EP4400168A3/en
Priority to PL15199455T priority patent/PL3018211T3/pl
Priority to EP15199455.5A priority patent/EP3018211B1/en
Priority to KR1020137006385A priority patent/KR101310569B1/ko
Priority to RS20160204A priority patent/RS54649B1/sr
Priority to AU2011296882A priority patent/AU2011296882B2/en
Priority to EP19188572.2A priority patent/EP3581655A1/en
Priority to EP19169673.1A priority patent/EP3543341A1/en
Priority to EP24168460.4A priority patent/EP4403632A3/en
Priority to ES11821996.3T priority patent/ES2567411T3/es
Application filed by Nippon Shinyaku Co Ltd, National Center of Neurology and Psychiatry filed Critical Nippon Shinyaku Co Ltd
Priority to CN201180042420.0A priority patent/CN103154245B/zh
Publication of WO2012029986A1 publication Critical patent/WO2012029986A1/ja
Anticipated expiration legal-status Critical
Priority to US14/615,504 priority patent/US9708361B2/en
Priority to SM201600111T priority patent/SMT201600111B/it
Priority to US15/619,996 priority patent/US10329319B2/en
Priority to US16/359,213 priority patent/US10385092B2/en
Priority to US16/364,451 priority patent/US10407461B2/en
Priority to US16/369,427 priority patent/US10487106B2/en
Priority to US16/408,529 priority patent/US10870676B2/en
Priority to US16/449,537 priority patent/US10647741B2/en
Priority to CY20191101075T priority patent/CY1122167T1/el
Priority to US16/712,686 priority patent/US10662217B2/en
Priority to US16/717,274 priority patent/US10683322B2/en
Priority to US17/126,366 priority patent/US20210179659A1/en
Priority to US17/175,276 priority patent/US11028122B1/en
Priority to US17/333,677 priority patent/US20210284680A1/en
Priority to US17/375,877 priority patent/US20210340171A1/en
Priority to US18/053,679 priority patent/US20230151050A1/en
Priority to US18/774,442 priority patent/US20250042933A1/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/04—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/7125—Nucleic acids or oligonucleotides having modified internucleoside linkage, i.e. other than 3'-5' phosphodiesters
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    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
    • C07K14/4707—Muscular dystrophy
    • C07K14/4708—Duchenne dystrophy
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • 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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    • C12N2310/00—Structure or type of the nucleic acid
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    • C12N2310/11—Antisense
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    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/30—Chemical structure
    • C12N2310/31—Chemical structure of the backbone
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    • C12N2310/00—Structure or type of the nucleic acid
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    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/30—Chemical structure
    • C12N2310/32—Chemical structure of the sugar
    • C12N2310/321—2'-O-R Modification
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    • C12N2310/30—Chemical structure
    • C12N2310/35—Nature of the modification
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    • C12N2310/3525—MOE, methoxyethoxy
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    • C12N2320/00—Applications; Uses
    • C12N2320/30—Special therapeutic applications
    • C12N2320/33—Alteration of splicing

Definitions

  • the present invention relates to an antisense oligomer that enables skipping of the 53rd exon of the human dystrophin gene and a pharmaceutical composition containing the oligomer.
  • DMD Duchenne muscular dystrophy
  • the dystrophin gene is present on the X chromosome and is a huge gene composed of 2.2 million base pairs of DNA.
  • Dystrophin protein is involved in maintaining the membrane stability of muscle cells, and is necessary to make muscle cells difficult to break. Since the dystrophin gene of DMD patients has a mutation, dystrophin protein having a function in muscle cells is hardly expressed. Therefore, in the DMD patient body, the structure of the muscle cell cannot be maintained, and a large amount of calcium ions flows into the muscle cell. As a result, a reaction similar to inflammation occurs and fibrosis advances, making it difficult for muscle cells to regenerate.
  • Becker muscular dystrophy is also caused by mutations in the dystrophin gene, but its symptoms generally show weakness due to muscle atrophy, but are generally lighter than DMD, and the progression of weakness is slow, often in adulthood.
  • the difference in clinical symptoms between DMD and BMD is thought to be due to whether the amino acid reading frame when dystrophin mRNA is translated into dystrophin protein due to mutation is destroyed or maintained (non-patented). Reference 1).
  • DMD has a mutation that shifts the amino acid reading frame, so that almost no functional dystrophin protein is expressed.
  • BMD a part of the exon is deleted due to the mutation, but the amino acid reading frame is maintained. Therefore, a dystrophin protein having a function although it is incomplete is produced.
  • the exon skipping method is expected as a treatment method for DMD.
  • This method restores the amino acid reading frame of dystrophin mRNA by altering splicing and induces the expression of dystrophin protein partially restored in function (Non-patent Document 2).
  • the part of the amino acid sequence targeted for exon skipping will be lost.
  • the dystrophin protein expressed by this treatment is shorter than the normal one, but the function of stabilizing muscle cells is partially retained because the amino acid reading frame is maintained.
  • exon skipping is expected to cause DMD to exhibit symptoms similar to milder BMD.
  • the exon skipping method is undergoing clinical trials for human DMD patients through animal experiments with mice and dogs.
  • Exon skipping can be induced by binding of antisense nucleic acids that target either or both 5 'or 3' splice sites, or the interior of an exon. Exons are only included in mRNA if both splice sites are recognized by the spliceosome complex. Thus, exon skipping can be induced by targeting the splice site with an antisense nucleic acid. In addition, it is thought that the binding of SR protein to exon splicing enhancer (ESE) is necessary for exon to be recognized by splicing mechanism, and exon skipping can also be induced by targeting ESE. it can.
  • ESE exon splicing enhancer
  • Non-patent Document 3 Since the mutation of the dystrophin gene varies depending on the DMD patient, an antisense nucleic acid corresponding to the location and type of the gene mutation is required. So far, antisense nucleic acids that induce exon skipping for all 79 exons have been produced by Steve Wilton et al. Of the University of Western Australia (Non-patent Document 3), and 39 kinds of antisense nucleic acids have been produced by Annemieke Aartsma-Rus et al. Of the Netherlands. An antisense nucleic acid that induces exon skipping relative to an exon has been made (Non-patent Document 4).
  • exon 53 About 8% of all DMD patients are considered to be treatable by skipping the 53rd exon (hereinafter referred to as “exon 53”).
  • exon 53 the 53rd exon
  • Patent Documents 1 to 4 Non-Patent Document 5
  • International Publication WO 2006/000057 International Publication WO 2004/048570 US Patent Publication US 2010/0168212 International Publication WO 2010/048586 Monaco A. P. et al. Genomics 1988; 2: p. 90-95 Matsuo M.M. Brain Dev 1996; 18: p. 167-172 Wilton S.
  • an antisense oligomer that strongly induces the skipping of exon 53 of the dystrophin gene and a therapeutic agent for muscular dystrophy containing the oligomer are desired.
  • the present inventors have found that nucleotides around the 32nd to 56th nucleotides from the 5 ′ end of exon 53 in the mRNA precursor of the dystrophin gene (hereinafter referred to as “pre-mRNA”). It was found that the skipping of exon 53 can be induced with high efficiency by targeting the sequence consisting of an antisense oligomer.
  • pre-mRNA nucleotides around the 32nd to 56th nucleotides from the 5 ′ end of exon 53 in the mRNA precursor of the dystrophin gene
  • An antisense oligomer that enables skipping of the 53rd exon of the human dystrophin gene, the 31st to 53rd, 31st to 54th from the 5 'end of the 53rd exon of the human dystrophin gene 31st to 55th, 31st to 56th, 31st to 57th, 31st to 58th, 32nd to 53rd, 32nd to 54th, 32nd to 55th, 32nd to 56th, 32 to 57, 32 to 58, 33 to 53, 33 to 54, 33 to 55, 33 to 56, 33 to 57, 33 to 58, 34 to 53rd, 34th to 54th, 34th to 55th, 34th to 56th, 34th to 57th, 34th to 58th, 35th to 53rd, 35th to 54th, 35th to 55th 35th to 56th, 35th to 57th, 35th to 58th, Complementary to any one of the sequences consisting of nucleotides 36 to 53, 36,
  • An antisense oligomer consisting of a base sequence.
  • the sugar moiety of at least one nucleotide constituting the oligonucleotide has a 2′-position —OH group, OR, R, R′OR, SH, SR, NH 2 , NHR, NR 2 , N 3 ,
  • the above R represents alkyl or aryl, and the above R ′ represents alkylene.
  • the phosphate-binding portion of at least one nucleotide constituting the oligonucleotide is selected from the group consisting of a phosphorothioate bond, a phosphorodithioate bond, an alkylphosphonate bond, a phosphoramidate bond, and a boranophosphate bond.
  • the antisense oligomer according to [1] which is a morpholino oligomer.
  • [7] The antisense oligomer according to [6], which is a phosphorodiamidate morpholino oligomer.
  • [8] The antisense oligomer according to any one of [1] to [7], wherein the 5 ′ end is any one of the following chemical formulas (1) to (3).
  • [9] The above [1] to [8], comprising a base sequence complementary to a sequence consisting of nucleotides 32 to 56 or 36 to 56 from the 5 ′ end of the 53 ′ exon of the human dystrophin gene. The antisense oligomer of any one of these.
  • a pharmaceutical composition for treating muscular dystrophy comprising the antisense oligomer according to any one of [1] to [12], a pharmaceutically acceptable salt or hydrate thereof as an active ingredient.
  • the antisense oligomer of the present invention can induce skipping of exon 53 of the human dystrophin gene with high efficiency. Moreover, the symptoms of Duchenne muscular dystrophy can be effectively reduced by administering the pharmaceutical composition of the present invention.
  • RD cell rhabdomyosarcoma cell line
  • Antisense oligomer The present invention is an antisense oligomer that enables skipping of the 53rd exon of the human dystrophin gene, which is 31st to 53rd, 31st to 54th from the 5 'end of the 53rd exon of the human dystrophin gene.
  • “gene” includes not only genomic genes but also cDNAs, mRNA precursors and mRNAs. Preferably, the gene is an mRNA precursor, ie pre-mRNA.
  • the human dystrophin gene is present at locus Xp21.2.
  • the human dystrophin gene has a size of 3.0 Mbp, and is the largest known human gene.
  • the coding region of the human dystrophin gene is only 14 kb, and the coding region is dispersed in the dystrophin gene as 79 exons (Roberts, RG., Et al., Genomics, 16: 536-538 ( 1993)).
  • Pre-mRNA a transcript of the human dystrophin gene, is spliced to produce a 14 kb mature mRNA.
  • the base sequence of the human wild-type dystrophin gene is known (GenBank Accession No. NM_004006).
  • the nucleotide sequence of exon 53 of the human wild type dystrophin gene is shown in SEQ ID NO: 1.
  • the oligomer of the present invention was prepared for the purpose of modifying a protein encoded by the DMD dystrophin gene into a BMD dystrophin protein by skipping exon 53 of the human dystrophin gene. Therefore, exon 53 of the dystrophin gene to be subjected to exon skipping of the oligomer of the present invention includes not only the wild type but also the mutant type.
  • the exon 53 of the mutant human dystrophin gene is specifically a polynucleotide described in (a) or (b) below.
  • A a polynucleotide that hybridizes under stringent conditions with a polynucleotide comprising a base sequence complementary to the base sequence of SEQ ID NO: 1;
  • B a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 1
  • polynucleotide means DNA or RNA.
  • the “polynucleotide hybridizing under stringent conditions” means, for example, a colony high using, as a probe, all or part of a polynucleotide comprising a base sequence complementary to the base sequence of SEQ ID NO: 1.
  • the “complementary base sequence” is not limited to a base sequence that forms a Watson-Crick pair with the target base sequence, but a base that forms a wobble base pair. Includes sequences.
  • the Watson-Crick pair means a base pair in which a hydrogen bond is formed between adenine-thymine, adenine-uracil and guanine-cytosine
  • the fluctuation base pair means guanine-uracil, inosine-uracil, inosine.
  • the “complementary base sequence” may not have 100% complementarity with the target base sequence.
  • stringent conditions may be any of low stringent conditions, medium stringent conditions, and high stringent conditions.
  • Low stringent conditions are, for example, conditions of 5 ⁇ SSC, 5 ⁇ Denhardt's solution, 0.5% SDS, 50% formamide, and 32 ° C.
  • Medium stringent conditions include, for example, 5 ⁇ SSC, 5 ⁇ Denhardt's solution, 0.5% SDS, 50% formamide, 42 ° C. or 5 ⁇ SSC, 1% SDS, 50 mM Tris-HCl (pH 7. 5) The conditions are 50% formamide and 42 ° C.
  • “High stringent conditions” are, for example, 5 ⁇ SSC, 5 ⁇ Denhardt's solution, 0.5% SDS, 50% formamide, 50 ° C. or 0.2 ⁇ SSC, 0.1% SDS, 65 ° C. is there. Under these conditions, it can be expected that a polynucleotide having high identity can be efficiently obtained as the temperature is increased.
  • factors affecting the stringency of hybridization include multiple factors such as temperature, probe concentration, probe length, ionic strength, time, and salt concentration, and those skilled in the art can select these factors as appropriate. By doing so, it is possible to achieve the same stringency.
  • Alkphos Direct Labeling and Detection System (GE Healthcare) can be used, for example.
  • incubation with the labeled probe is performed overnight, and then the membrane is washed with a primary washing buffer containing 0.1% (w / v) SDS at 55 ° C. After washing, the hybridized polynucleotide can be detected.
  • a probe based on all or part of the base sequence complementary to the base sequence of SEQ ID NO: 1 using a commercially available reagent (for example, PCR labeling mix (Roche Diagnostics) etc.)
  • a commercially available reagent for example, PCR labeling mix (Roche Diagnostics) etc.
  • DIG digoxigenin
  • hybridization can be detected using a DIG nucleic acid detection kit (Roche Diagnostics).
  • polynucleotide other than the hybridizable polynucleotide 90% or more, 91% or more of the polynucleotide of SEQ ID NO: 1, when calculated using the default parameters by BLAST, which is homology search software, 92% or more, 93% or more, 94% or more, 95% or more, 96% or more, 97% or more, 98% or more, 99% or more, 99.1% or more, 99.2% or more, 99.3% or more, A polynucleotide having 99.4% or more, 99.5% or more, 99.6% or more, 99.7% or more, 99.8% or more, or 99.9% or more can be mentioned.
  • the identity of the base sequence is the algorithm BLAST (Basic Local Alignment Search Tool) (Proc. Natl. Acad. Sci. USA 872624-2268, 1990; Proc Natl Acad Sci USA 93: 5873) by Carlin and Arthur. Can be determined.
  • Programs called BLASTN and BLASTX based on the BLAST algorithm have been developed (Altschul SF, et al: J Mol Biol 215: 403, 1990).
  • the default parameters of each program are used.
  • the oligomer of the present invention is preferably 32 to 56, 33 to 56, 34 to 56, 35 to 56, or 36 to 36 from the 5 'end of the 53rd exon of the human dystrophin gene. It consists of a base sequence complementary to any one of the sequences consisting of the 56th nucleotide (for example, SEQ ID NO: 11, SEQ ID NO: 17, SEQ ID NO: 23, SEQ ID NO: 29, or SEQ ID NO: 35).
  • the oligomer of the present invention is a base sequence complementary to any one of the sequences consisting of nucleotides 32 to 56 or 36 to 56 from the 5 ′ end of the 53rd exon of the human dystrophin gene.
  • “Enabling the skipping of the 53rd exon of the human dystrophin gene” means that the oligomer of the present invention binds to a site corresponding to exon 53 of a transcript of the human dystrophin gene (eg, pre-mRNA).
  • a transcript of the human dystrophin gene eg, pre-mRNA.
  • the transcript is spliced, for example, in the case of a DMD patient in which exon 52 is deleted, the base corresponding to the 5 ′ end of exon 54 is located on the 3 ′ side of the base sequence corresponding to the 3 ′ end of exon 51. It means that a mature mRNA is formed in which the sequences are linked and no codon frameshift occurs.
  • the oligomer of the present invention may not have a base sequence that is 100% complementary to the target sequence as long as exon 53 of the human dystrophin gene can be skipped.
  • the oligomer of the present invention may contain 1 to 3, 1 to 2, or 1 non-complementary base with respect to the target sequence.
  • the “binding” means that when the oligomer of the present invention and the transcript of the human dystrophin gene are mixed, they hybridize to form a double strand under physiological conditions.
  • the “physiological condition” means a condition adjusted to a pH, salt composition, and temperature similar to those in a living body.
  • the conditions include 25 to 40 ° C., preferably 37 ° C., pH 5 to 8, preferably pH 7.4, and a sodium chloride concentration of 150 mM.
  • Whether or not the exon 53 of the human dystrophin gene skipped occurred was determined by introducing the oligomer of the present invention into a dystrophin-expressing cell (for example, human rhabdomyosarcoma cell), and from the total RNA of the dystrophin-expressing cell, It can be confirmed by performing RT-PCR amplification on the peripheral region of exon 53 of mRNA and performing nested PCR or sequence analysis on the PCR amplification product. The skipping efficiency was determined by recovering mRNA of the human dystrophin gene from the test cells.
  • a dystrophin-expressing cell for example, human rhabdomyosarcoma cell
  • the oligomer of the present invention include oligonucleotides, morpholino oligomers, and peptide nucleic acid (Peptide Nucleic Acid: PNA) oligomers having a length of 18 to 28 bases. A length of 21 to 25 bases is preferred, and a morpholino oligomer is preferred.
  • oligonucleotide of the present invention is an oligomer of the present invention having nucleotide as a structural unit, and such nucleotide may be any of ribonucleotide, deoxyribonucleotide, or modified nucleotide.
  • Modified nucleotides are those in which all or part of the nucleobase, sugar moiety, and phosphate binding moiety constituting ribonucleotide or deoxyribonucleotide are modified.
  • the nucleobase include adenine, guanine, hypoxanthine, cytosine, thymine, uracil, and modified bases thereof.
  • modified base examples include pseudouracil, 3-methyluracil, dihydrouracil, 5-alkylcytosine (eg, 5-methylcytosine), 5-alkyluracil (eg, 5-ethyluracil), 5-halouracil (5 -Bromouracil), 6-azapyrimidine, 6-alkylpyrimidine (6-methyluracil), 2-thiouracil, 4-thiouracil, 4-acetylcytosine, 5- (carboxyhydroxymethyl) uracil, 5'-carboxymethylaminomethyl 2-thiouracil, 5-carboxymethylaminomethyluracil, 1-methyladenine, 1-methylhypoxanthine, 2,2-dimethylguanine, 3-methylcytosine, 2-methyladenine, 2-methylguanine, N6-methyladenine 7-Methylguani 5-methoxyaminomethyl-2-thiouracil, 5-methylaminomethyluracil, 5-methylcarbonylmethyluracil, 5-methyloxyurac
  • modification of the sugar moiety examples include modification of the 2 'position of ribose and modification of other parts of the sugar.
  • modification of the 2'-position of ribose examples include, for example, the -OH group at the 2'-position of ribose is OR, R, R'OR, SH, SR, NH 2 , NMR, NR 2 , N 3 , CN, F, Cl, Br, and I can be substituted.
  • R represents alkyl or aryl.
  • Examples of the modification of the other part of the sugar include, for example, those in which O at the 4′-position of ribose or deoxyribose is replaced with S, and those in which the 2′-position and 4′-position of the sugar are cross-linked, such as LNA (Locked Nucleic Acid ) Or ENA (2′-O, 4′-C-Ethylene-bridged Nucleic Acids), but is not limited thereto.
  • LNA Locked Nucleic Acid
  • ENA (2′-O, 4′-C-Ethylene-bridged Nucleic Acids
  • Examples of the modification of the phosphate binding moiety include a phosphodiester bond, a phosphorothioate bond, a phosphorodithioate bond, an alkyl phosphonate bond, a phosphoramidate bond, a boranophosphate bond (Enya et al: Bioorganic & Medicinal Chemistry, 2008). , 18, 9154-9160) (see, for example, Patent Reissue Publication Nos. 2006/129594 and 2006/038608).
  • As the alkyl linear or branched alkyl having 1 to 6 carbon atoms is preferable.
  • cycloalkyl is preferably a cycloalkyl having 5 to 12 carbon atoms.
  • Alkoxy includes linear or branched alkoxy having 1 to 6 carbon atoms, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n- Examples include pentyloxy, isopentyloxy, n-hexyloxy, isohexyloxy and the like.
  • alkoxy having 1 to 3 carbon atoms is preferable.
  • aryl aryl having 6 to 10 carbon atoms is preferable. Specific examples include phenyl, ⁇ -naphthyl, and ⁇ -naphthyl. Particularly preferred is phenyl.
  • the aryl may be substituted, and examples of the substituent include alkyl, halogen, alkoxy, cyano, and nitro, and 1 to 3 of these may be substituted.
  • the alkylene is preferably a linear or branched alkylene having 1 to 6 carbon atoms.
  • acyl examples include linear or branched alkanoyl or aroyl.
  • alkanoyl examples include formyl, acetyl, 2-methylacetyl, 2,2-dimethylacetyl, propionyl, butyryl, isobutyryl, pentanoyl, 2,2-dimethylpropionyl, hexanoyl and the like.
  • aroyl examples include benzoyl, toluoyl, and naphthoyl.
  • the oligonucleotide of the present invention preferably has a group represented by the following general formula, wherein the —OH group at the 2′-position of ribose is substituted with methoxy, and the phosphate bond portion is a phosphorothioate bond. Oligomer. (In the formula, Base represents a nucleobase.)
  • the oligonucleotide of the present invention can be easily synthesized using various automatic synthesizers (for example, AKTA oligopilot plus 10/100 (GE Healthcare)), or a third-party organization (for example, Promega or It can also be manufactured by consigning to Takara).
  • the morpholino oligomer of the present invention is an oligomer of the present invention having a group represented by the following general formula as a structural unit.
  • Base is as defined above; W represents a group represented by any of the following formulas.
  • X is —CH 2 R 1 , -O-CH 2 R 1 , -S-CH 2 R 1 , -NR 2 R 3 Or represents F;
  • R 2 And R 3 Are the same or different and each represents H, alkyl, cycloalkyl, or aryl;
  • Z represents O or S.
  • the morpholino oligomer is preferably an oligomer (a phosphorodiamidate morpholino oligomer (hereinafter referred to as “PMO”)) having a group represented by the following formula as a structural unit. (In the formula, Base, R 2 , R 3 Is as defined above. )
  • PMO phosphorodiamidate morpholino oligomer
  • the morpholino oligomer can be produced according to, for example, International Publication No. 1991/009033 or International Publication No. 2009/064471.
  • PMO can be produced according to the method described in International Publication No. 2009/064471, or can be produced according to the method described below.
  • PMO manufacturing method As one embodiment of PMO, for example, a compound represented by the following general formula (I) (hereinafter referred to as PMO (I)) can be mentioned. [Where each Base, R 2 , R 3 Is as defined above; N is an arbitrary integer in the range of 1 to 99, preferably an arbitrary integer in the range of 18 to 28. ] PMO (I) can be produced according to a known method, but can be produced, for example, by carrying out the following steps. The compounds and reagents used in the following steps are not particularly limited as long as they are generally used in the production of PMO.
  • n, R 2 , R 3 Is as defined above; Each B P Independently represents an optionally protected nucleobase; T represents a trityl group, a monomethoxytrityl group, or a dimethoxytrityl group; L represents hydrogen, acyl, or a group represented by the following general formula (IV) (hereinafter referred to as group (IV)). ]
  • B P Examples of the “nucleobase” include the same “nucleobase” as Base. However, B P The amino group or hydroxyl group of the nucleobase according to the above may be protected. The amino-protecting group is not particularly limited as long as it is used as a protecting group for nucleic acids.
  • the hydroxyl-protecting group include 2-cyanoethyl, 4-nitrophenethyl, phenylsulfonylethyl, methylsulfonylethyl, trimethylsilylethyl, substituted with 1 to 5 electron-withdrawing groups at any substitutable position.
  • the “solid phase carrier” is not particularly limited as long as it is a carrier that can be used for a solid phase reaction of nucleic acid.
  • a reagent that can be used for synthesis of a morpholino nucleic acid derivative for example, dichloromethane, acetonitrile, tetrazole, N-methylimidazole, pyridine, acetic anhydride, lutidine, trifluoroacetic acid
  • chemically stable to reagents that can be used to synthesize morpholino nucleic acid derivatives for example, dichloromethane, acetonitrile, tetrazole, N-methylimidazole, pyridine, acetic anhydride, lutidine, trifluoroacetic acid
  • chemical modification (Iv) can be loaded with the desired morpholino nucleic acid derivative, (v) has sufficient strength to withstand the high pressures during processing, and (vi) has a certain particle size range and distribution.
  • swellable polystyrene for example, aminomethylpolystyrene resin, 1% dibenzylbenzene crosslinked (200 to 400 mesh) (2.4 to 3.0 mmol / g) (manufactured by Tokyo Chemical Industry Co., Ltd.), Aminomethylated Polystyrene Resin ⁇ HCl [Dibenzylbenzene 1%, 100-200 mesh] (Peptide Laboratories)), non-swellable polystyrene (for example, Primer Support (GE, Healthcare)), PEG chain-bonded polystyrene (for example, NH 2 -PEG resin (manufactured by Watanabe Chemical), TentaGel resin, controlled pore glass (CPG) (for example, manufactured by CPG), oxalylated-constant glass (for example, Allul et al., Nucleic Acids Research, Vol.
  • CPG controlled pore glass
  • oxalylated-constant glass for
  • Examples of the “acid” that can be used in this step include trifluoroacetic acid, dichloroacetic acid, and trichloroacetic acid.
  • the amount of the acid used is, for example, suitably in the range of 0.1 molar equivalent to 1000 molar equivalents, and preferably in the range of 1 molar equivalent to 100 molar equivalents, relative to 1 mole of compound (II).
  • an organic amine can be used together with the acid. Although it does not specifically limit as an organic amine, For example, a triethylamine can be mentioned.
  • the amount of the organic amine used is, for example, suitably in the range of 0.01 molar equivalent to 10 molar equivalents, and preferably in the range of 0.1 molar equivalents to 2 molar equivalents with respect to 1 mole of the acid. .
  • a salt or mixture of an acid and an organic amine in this step for example, a salt or mixture of trifluoroacetic acid and triethylamine can be mentioned, and more specifically, with respect to 2 equivalents of trifluoroacetic acid. What mixed 1 equivalent of triethylamine can be mentioned.
  • the acid that can be used in this step can be used by diluting with an appropriate solvent so that the concentration is in the range of 0.1% to 30%.
  • the solvent is not particularly limited as long as it does not participate in the reaction, and examples thereof include dichloromethane, acetonitrile, alcohols (ethanol, isopropanol, trifluoroethanol, etc.), water, and mixtures thereof.
  • the reaction temperature in the above reaction is, for example, preferably within the range of 10 ° C. to 50 ° C., more preferably within the range of 20 ° C. to 40 ° C., and further preferably within the range of 25 ° C. to 35 ° C.
  • the reaction time varies depending on the type of acid used and the reaction temperature, but it is usually within the range of 0.1 minute to 24 hours. Preferably, it is within the range of 1 minute to 5 hours.
  • a base can be added as necessary to neutralize the acid present in the system.
  • the “base” is not particularly limited, and examples thereof include diisopropylamine.
  • the base can be used by diluting with a suitable solvent so that the concentration is within the range of 0.1% (v / v) to 30% (v / v).
  • the solvent used in this step is not particularly limited as long as it does not participate in the reaction, and examples thereof include dichloromethane, acetonitrile, alcohols (ethanol, isopropanol, trifluoroethanol, etc.), water, or a mixture thereof.
  • the reaction temperature is, for example, preferably in the range of 10 ° C.
  • reaction time varies depending on the type of base used and the reaction temperature, but is usually in the range of 0.1 minute to 24 hours, and preferably in the range of 1 minute to 5 hours.
  • the compound represented by the following general formula (IIa) (hereinafter referred to as compound (IIa)) is prepared by the following method. Can be manufactured according to. [Where B P , T, linker, and solid phase carrier are as defined above.
  • Step 1 The process of manufacturing the compound (henceforth a compound (VI)) represented by the following general formula (VI) by making an acylating agent act on the compound represented by the following general formula (V).
  • This step can be carried out by a known linker introduction reaction using compound (V) as a starting material.
  • the compound represented by the following general formula (VIa) can be produced by carrying out a method known as an esterification reaction using compound (V) and succinic anhydride.
  • B P , T are as defined above.
  • Step 2 A step of producing a compound (IIa) by reacting with a solid phase carrier by allowing a condensing agent or the like to act on the compound (VI).
  • This step can be produced by a method known as a condensation reaction using compound (VI) and a solid phase carrier.
  • n 2 to 99 and L is the group (IV)
  • the compound represented by the following general formula (IIa2) is obtained by using the compound (IIa) as a starting material, It can be manufactured by repeatedly performing Step A and Step B according to the method for producing PMO as described in the above.
  • the compound represented by the following general formula (IIb) is obtained by, for example, the method described in International Publication No. 1991/009033. Can be manufactured.
  • the compound represented by the following general formula (IIb2) is obtained by using the compound (IIb) as a starting material. It can be manufactured by repeatedly performing Step A and Step B according to the PMO manufacturing method a desired number of times.
  • Process B A step of producing a compound represented by the following general formula (VII) (hereinafter referred to as compound (VII)) by allowing a morpholino monomer compound to act on compound (III) in the presence of a base.
  • VII general formula
  • This step can be carried out by reacting compound (III) with a morpholino monomer compound in the presence of a base.
  • Examples of the morpholino monomer compound include a compound represented by the following general formula (VIII).
  • Examples of the “base” that can be used in this step include diisopropylamine, triethylamine, and N-ethylmorpholine.
  • the amount of the base used is, for example, suitably in the range of 1 molar equivalent to 1000 molar equivalents, preferably in the range of 10 molar equivalents to 100 molar equivalents, relative to 1 mole of compound (III).
  • the morpholino monomer compound and base that can be used in this step can be diluted with an appropriate solvent so as to have a concentration of 0.1% to 30%.
  • the solvent is not particularly limited as long as it does not participate in the reaction, and examples thereof include N, N-dimethylimidazolidone, N-methylpiperidone, DMF, dichloromethane, acetonitrile, terahydrofuran, and mixtures thereof.
  • the reaction temperature is preferably in the range of 0 ° C. to 100 ° C., for example, and more preferably in the range of 10 ° C. to 50 ° C.
  • the reaction time varies depending on the type of base used and the reaction temperature, but is usually within the range of 1 minute to 48 hours, and preferably within the range of 30 minutes to 24 hours. Further, after the completion of this step, an acylating agent can be added as necessary.
  • acylating agent examples include acetic anhydride, acetic chloride, and phenoxyacetic anhydride.
  • the acylating agent can be used by diluting with an appropriate solvent so that the concentration is within a range of 0.1% to 30%, for example.
  • the solvent is not particularly limited as long as it does not participate in the reaction, and examples thereof include dichloromethane, acetonitrile, alcohols (ethanol, isopropanol, trifluoroethanol, etc.), water, and mixtures thereof.
  • a base such as pyridine, lutidine, collidine, triethylamine, diisopropylethylamine, N-ethylmorpholine can be used together with an acylating agent.
  • the amount of the acylating agent used is preferably in the range of 0.1 molar equivalent to 10,000 molar equivalents, and more preferably in the range of 1 molar equivalent to 1000 molar equivalents.
  • the amount of the base used is, for example, suitably in the range of 0.1 molar equivalent to 100 molar equivalents, preferably in the range of 1 molar equivalent to 10 molar equivalents per mole of acylating agent.
  • the reaction temperature of this reaction is preferably within the range of 10 ° C to 50 ° C, more preferably within the range of 10 ° C to 50 ° C, more preferably within the range of 20 ° C to 40 ° C, and even more preferably. Is in the range of 25 ° C to 35 ° C.
  • Process C A step of producing a compound represented by the general formula (IX) by removing a protecting group using a deprotecting agent in the compound (VII) produced in the step B.
  • This step can be carried out by allowing a deprotecting agent to act on compound (VII).
  • Examples of the “deprotecting agent” include concentrated aqueous ammonia and methylamine.
  • the “deprotecting agent” that can be used in this step is, for example, diluted with water, methanol, ethanol, isopropyl alcohol, acetonitrile, tetrahydrofuran, DMF, N, N-dimethylimidazolidone, N-methylpiperidone, or a mixed solvent thereof. It can also be used. Of these, ethanol is preferred.
  • the amount of the deprotecting agent to be used is, for example, suitably in the range of 1 molar equivalent to 100,000 molar equivalents, preferably in the range of 10 molar equivalents to 1000 molar equivalents, relative to 1 mole of compound (VII). It is.
  • the reaction temperature is, for example, suitably in the range of 15 ° C.
  • Process D Process of manufacturing PMO (I) by making an acid act on the compound (IX) manufactured in the process C. [In the formula, Base, n, R 2 , R 3 , T are as defined above. ] This step can be carried out by adding an acid to compound (IX).
  • Examples of the “acid” that can be used in this step include trichloroacetic acid, dichloroacetic acid, acetic acid, phosphoric acid, and hydrochloric acid.
  • the amount of the acid used is, for example, suitably so that the pH of the solution is in the range of 0.1 to 4.0, more preferably in the range of 1.0 to 3.0.
  • the solvent is not particularly limited as long as it does not participate in the reaction, and examples thereof include acetonitrile, water, and mixed solvents thereof.
  • the reaction temperature is preferably in the range of 10 ° C to 50 ° C, more preferably in the range of 20 ° C to 40 ° C, and still more preferably in the range of 25 ° C to 35 ° C.
  • the deprotection reaction time varies depending on the type of compound (IX), reaction temperature, etc., but is suitably in the range of 0.1 minute to 5 hours, preferably in the range of 1 minute to 1 hour, more preferably. Is in the range of 1 to 30 minutes.
  • PMO (I) is a conventional separation and purification means from the reaction mixture obtained in this step, such as extraction, concentration, neutralization, filtration, centrifugation, recrystallization, C 8 To C 18 Obtained by using reverse phase column chromatography, cation exchange column chromatography, anion exchange column chromatography, gel filtration column chromatography, high performance liquid chromatography, dialysis, ultrafiltration or the like alone or in combination.
  • the desired PMO (I) can be isolated and purified (see, for example, International Publication No. WO1991 / 09033).
  • a mixed solution of 20 mM triethylamine / acetic acid buffer and acetonitrile can be used as an elution solvent.
  • a mixed solution of 1 M saline and 10 mM sodium hydroxide aqueous solution can be used.
  • the peptide nucleic acid is an oligomer of the present invention having a group represented by the following general formula as a structural unit.
  • Peptide nucleic acid can be produced, for example, according to the following literature. 1) P.I. E. Nielsen, M.M. Egholm, R.A. H. Berg, O .; Buchardt, Science, 254, 1497 (1991) 2) M.M. Egholm, O .; Buchardt, P.M. E. Nielsen, R.A. H. Berg, Jacs. , 114, 1895 (1992) 3) K.K. L. Dueholm, M.M. Egholm, C.I. Behrens, L.M. Christensen, H.C. F. Hansen, T .; Vulpius, K.M. H.
  • the 5 ′ end may be any group represented by the following chemical formulas (1) to (3).
  • (3) -OH is preferred.
  • the groups represented by the above (1), (2) and (3) are referred to as “group (1)”, “group (2)” and “group (3)”, respectively.
  • Pharmaceutical composition The oligomer of the present invention enables exon 53 to be skipped with high efficiency as compared with the antisense oligomer according to the prior art.
  • the symptoms of muscular dystrophy can be alleviated with high efficiency by administering a pharmaceutical composition containing the oligomer of the present invention to a DMD patient.
  • a pharmaceutical composition for treating muscular dystrophy hereinafter referred to as “the composition of the present invention” comprising the oligomer of the present invention, a pharmaceutically acceptable salt or hydrate thereof as an active ingredient.
  • Examples of the pharmaceutically acceptable salt of the oligomer of the present invention contained in the composition of the present invention include alkali metal salts such as sodium salt, potassium salt and lithium salt, alkaline earth such as calcium salt and magnesium salt.
  • the oligomer of the present invention contained in the composition of the present invention may be in the form of its hydrate.
  • the dosage form of the composition of the present invention is not particularly limited as long as it is a pharmaceutically acceptable dosage form, and can be selected depending on the treatment method. From the viewpoint of ease of delivery to muscle tissue, intravenous administration is possible. Internal administration, intraarterial administration, intramuscular administration, subcutaneous administration, oral administration, intratissue administration, transdermal administration and the like are preferred.
  • the dosage form that the composition of the present invention can take is not particularly limited, and examples thereof include various injections, oral preparations, instillations, inhalants, ointments, lotions and the like.
  • the composition of the present invention preferably contains a carrier that facilitates delivery of the oligomer to muscle tissue.
  • a carrier is not particularly limited as long as it is pharmaceutically acceptable, and examples thereof include cationic carriers such as cationic liposomes and cationic polymers, and carriers utilizing a viral envelope.
  • cationic liposomes include liposomes formed with 2-O- (2-diethylaminoethyl) carbamoyl-1,3-O-dioleoylglycerol and phospholipid as essential components (hereinafter, “liposome A”).
  • Oligofectamine (registered trademark) (manufactured by Invitrogen), Lipofectin (registered trademark) (manufactured by Invitrogen), Lipofectamine (registered trademark) (manufactured by Invitrogen), Lipofectamine 2000 (registered trademark) (manufactured by Invitrogen) DMRIE-C (registered trademark) (manufactured by Invitrogen), GeneSilencer (registered trademark) (manufactured by Gene Therapy Systems), TransMessenger (registered trademark) (manufactured by QIAGEN) TransIT TKO (registered trademark) (manufactured by Mirus, Inc.), can be mentioned Nucleofector II (Lonza).
  • liposome A is preferable.
  • the cationic polymer include JetSI (registered trademark) (manufactured by Qbiogene) and Jet-PEI (registered trademark) (polyethyleneimine, manufactured by Qbiogene).
  • the carrier using the virus envelope include GenomeOne (registered trademark) (HVJ-E liposome, manufactured by Ishihara Sangyo Co., Ltd.).
  • a pharmaceutical device described in Japanese Patent No. 2924179, and a cationic carrier described in Japanese Patent Publication No. 2006/129594 and Japanese Patent Publication No. 2008/096690 can be used.
  • the concentration of the oligomer of the present invention contained in the composition of the present invention varies depending on the type of carrier and the like, but is suitably in the range of 0.1 nM to 100 ⁇ M, preferably in the range of 1 nM to 10 ⁇ M, and in the range of 10 nM to 1 ⁇ M. Within the range is more preferable.
  • the weight ratio of the oligomer of the present invention to the carrier contained in the composition of the present invention (carrier / oligomer of the present invention) varies depending on the properties of the oligomer and the type of the carrier, but is 0.1 to 100. The range is suitable, preferably in the range of 1-50, more preferably in the range of 10-20.
  • a pharmaceutically acceptable additive can be optionally added to the composition of the present invention.
  • additives include emulsification aids (for example, fatty acids having 6 to 22 carbon atoms and pharmaceutically acceptable salts thereof, albumin, dextran), stabilizers (for example, cholesterol, phosphatidic acid), and isotonicity.
  • Agents for example, sodium chloride, glucose, maltose, lactose, sucrose, trehalose
  • pH adjusters for example, hydrochloric acid, sulfuric acid, phosphoric acid, acetic acid, sodium hydroxide, potassium hydroxide, triethanolamine.
  • hydrochloric acid sulfuric acid, phosphoric acid, acetic acid, sodium hydroxide, potassium hydroxide, triethanolamine.
  • the content of the additive in the composition of the present invention is suitably 90% by weight or less, preferably 70% by weight or less, and more preferably 50% by weight or less.
  • the composition of the present invention can be prepared by adding the oligomer of the present invention to a carrier dispersion and stirring appropriately.
  • the additive can be added in an appropriate step before or after the addition of the oligomer of the present invention.
  • the aqueous solvent that can be used when the oligomer of the present invention is added is not particularly limited as long as it is pharmaceutically acceptable, and examples thereof include electrolyte solutions such as water for injection, distilled water for injection, and physiological saline, and glucose. Examples thereof include sugar liquids such as liquid and maltose liquid.
  • the composition of the present invention can be, for example, a solution or a lyophilized preparation thereof.
  • the lyophilized preparation can be prepared by lyophilizing the composition of the present invention having a liquid form according to a conventional method. For example, after appropriately sterilizing the composition of the present invention in the form of a liquid agent, a predetermined amount is dispensed into a vial and pre-freezing for about 2 hours at about ⁇ 40 to ⁇ 20 ° C. And primary drying under reduced pressure at about 0-10 ° C., followed by secondary drying under reduced pressure at about 15-25 ° C. and lyophilization.
  • the inside of the vial is replaced with nitrogen gas and stoppered to obtain a lyophilized preparation of the composition of the present invention.
  • the freeze-dried preparation of the composition of the present invention can be used by re-dissolving generally by adding any appropriate solution (re-dissolving solution). Examples of such redissolved solution include water for injection, physiological saline, and other general infusion solutions.
  • re-dissolving solution examples include water for injection, physiological saline, and other general infusion solutions.
  • the amount of the redissolved solution varies depending on the use and the like and is not particularly limited. However, an amount of 0.5 to 2 times the amount of the solution before lyophilization or 500 mL or less is appropriate.
  • the dose for administration of the composition of the present invention is determined in consideration of the type of oligomer of the present invention, dosage form, patient condition such as age and weight, administration route, nature and degree of disease.
  • the amount of the oligomer of the present invention for adults is generally within the range of 0.1 mg to 10 g / human, preferably within the range of 1 mg to 1 g / human. This value may vary depending on the type of target disease, dosage form, and target molecule. Therefore, in some cases, a lower dose may be sufficient, and conversely, a higher dose may be required.
  • it can be administered once to several times a day or at intervals of 1 day to several days.
  • composition of the present invention there can be mentioned a pharmaceutical composition
  • a pharmaceutical composition comprising a vector capable of expressing the oligonucleotide of the present invention and the above-mentioned carrier.
  • Such an expression vector may be capable of expressing a plurality of the oligonucleotides of the present invention.
  • a pharmaceutically acceptable additive can be added to the composition.
  • concentration of the expression vector contained in the composition varies depending on the type of carrier and the like, but is suitably in the range of 0.1 nM to 100 ⁇ M, preferably in the range of 1 nM to 10 ⁇ M, and in the range of 10 nM to 1 ⁇ M. More preferred.
  • the weight ratio (carrier / expression vector) between the expression vector and the carrier contained in the composition varies depending on the nature of the expression vector, the type of the carrier, etc., but is suitably within the range of 0.1 to 100. It is preferably in the range of ⁇ 50, more preferably in the range of 10-20. Further, the content of the carrier contained in the composition is the same as that of the composition of the present invention containing the oligomer of the present invention, and the preparation method thereof is the same as that of the composition of the present invention. It is.
  • the present invention will be described in more detail with reference to examples and test examples, but the present invention is not limited to the scope shown in the examples.
  • Step 2 4- ⁇ [(2S, 6R) -6- (4-Benzamido-2-oxopyrimidin-1-yl) -4-tritylmorpholin-2-yl] methoxy ⁇ -supported on aminomethylpolystyrene resin
  • 4-oxobutanoic acid 4- ⁇ [(2S, 6R) -6- (4-benzamido-2-oxopyrimidin-1 (2H) -yl) -4-tritylmorpholin-2-yl] methoxy ⁇ -4-oxobutanoic acid 23.5 g It melt
  • the resin was collected by filtration, washed with pyridine, methanol and dichloromethane in this order, and dried under reduced pressure to obtain 33.7 g of the desired product.
  • the loading amount of the target product was determined by measuring the UV absorbance at 409 nm of the molar amount of trityl per gram of resin using a known method. The resin loading was 397.4 ⁇ mol / g.
  • Step 2 N- ⁇ 9-[(2R, 6S) -6- (hydroxymethyl) -4-morpholin-2-yl] -6-oxo-6,9-dihydro-1H-purin-2-yl ⁇ - 2-phenoxyacetamide p-toluenesulfonate
  • 30 g of the compound obtained in Step 1 was suspended in 480 mL of methanol, and 130 mL of 2N hydrochloric acid was added under ice cooling. Subsequently, 56.8 g of ammonium tetraborate tetrahydrate and 16.2 g of sodium periodate were added in this order, and the mixture was stirred at room temperature for 3 hours.
  • the reaction solution was ice-cooled, insoluble matter was removed by filtration, and this was washed with 100 mL of methanol. The filtrate and the washing solution were combined and ice-cooled. After adding 11.52 g of 2-picoline borane and stirring for 20 minutes, 54.6 g of p-toluenesulfonic acid monohydrate was slowly added and stirred overnight at 4 ° C. . The precipitate was collected by filtration, washed with 500 mL of cold methanol, and dried to obtain 17.7 g of the target compound (yield: 43.3%).
  • Step 4 4-oxo-4- ⁇ [(2S, 6R) -6- (6-oxo-2- [2-phenoxyacetamide] -1H-purin-9-yl supported on aminomethylpolystyrene resin ) -4-Tritylmorpholin-2-yl] methoxy ⁇ butanoic acid
  • the title compound was produced in the same manner as in Reference Example 1.
  • N- ⁇ 9-[(2R, 6S) -6- (hydroxymethyl) -4-tritylmorpholin-2-yl] -6-oxo-6,9 -Dihydro-1H-purin-2-yl ⁇ -2-phenoxyacetamide was used.
  • 1-[(2R, 6S) -6- (hydroxymethyl) -4-tritylmorpholin-2-yl] -5-methylpyrimidine-2,4 (1H , 3H) -dione was used.
  • 2- [2- (2-hydroxyethoxy) ethoxy] ethyl 4-tritylpiperazine-1-carboxylic acid (a compound described in International Publication No. 2009/064471) )It was used.
  • PMO No. 12 was purchased from Gene Tools.
  • PMO No. 8 4- ⁇ [(2S, 6R) -6- (4-benzamido-2-oxopyrimidin-1 (2H) -yl) -4-tritylmorpholin-2-yl] methoxy ⁇ -supported on aminomethylpolystyrene resin 2 g (800 ⁇ mol) of 4-oxobutanoic acid (Reference Example 1) was transferred to a reaction vessel, 30 mL of dichloromethane was added, and the mixture was allowed to stand for 30 minutes.
  • the neutralizing solution a solution obtained by dissolving N, N-diisopropylethylamine in a dichloromethane solution containing 25% (v / v) 2-propanol so as to be 5% (v / v) was used.
  • the coupling solution A the morpholino monomer compound was dissolved in 1,3-dimethyl-2-imidazolidinone containing 10% (v / v) N, N-diisopropylethylamine so as to be 0.15 M. A thing was used.
  • N, N-diisopropylethylamine dissolved in 1,3-dimethyl-2-imidazolidinone so as to be 10% (v / v) was used.
  • a capping solution 20% (v / v) acetic anhydride and 30% (v / v) 2,6-lutidine dissolved in dichloromethane were used.
  • the aminomethylpolystyrene resin carrying PMO synthesized above was collected from the reaction vessel and dried under reduced pressure at room temperature for 2 hours or more.
  • PMO supported on the dried aminomethylpolystyrene resin was placed in a reaction vessel, and 200 mL of 28% aqueous ammonia-ethanol (1/4) was added, followed by stirring at 55 ° C. for 15 hours.
  • the aminomethyl polystyrene resin was filtered off and washed with 50 mL of water-ethanol (1/4).
  • the obtained filtrate was concentrated under reduced pressure.
  • the obtained residue was dissolved in 100 mL of a mixed solvent (4/1) of 20 mM acetic acid-triethylamine buffer (TEAA buffer) and acetonitrile, and filtered through a membrane filter.
  • the resulting filtrate was purified by reverse phase HPLC.
  • the conditions used are as follows.
  • each fraction was analyzed, and the target product was recovered with 100 mL of acetonitrile-water (1/1), 200 mL of ethanol was added, and the mixture was concentrated under reduced pressure. Furthermore, it dried under reduced pressure and obtained white solid. 300 mL of a 10 mM phosphoric acid aqueous solution was added to the obtained solid and suspended. 10 mL of 2M phosphoric acid aqueous solution was added and stirred for 15 minutes. Furthermore, 15 mL of 2M sodium hydroxide aqueous solution was added and neutralized. Furthermore, 15 mL of 2M sodium hydroxide aqueous solution was added to make it alkaline, and the mixture was filtered with a membrane filter (0.45 ⁇ m).
  • the target product was obtained as an aqueous solution by washing with 100 mL of 10 mM sodium hydroxide aqueous solution.
  • the obtained aqueous solution containing the target product was purified with an anion exchange resin column.
  • the conditions used are as follows. Each fraction was analyzed (HPLC) to obtain the target product as an aqueous solution.
  • the resulting aqueous solution was neutralized by adding 225 mL of 0.1 M phosphate buffer (pH 6.0). It filtered with the membrane filter (0.45 micrometer). Subsequently, it desalted by performing ultrafiltration under the following conditions.
  • the filtrate was concentrated to obtain about 250 mL of an aqueous solution.
  • the obtained aqueous solution was filtered with a membrane filter (0.45 ⁇ m).
  • Example 5 The title compound was produced in the same manner as in Example 1. However, 4-((((2S, 6R) -6- (5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1 (2H) -yl) supported on aminomethylpolystyrene resin as a starting material ) -4-Tritylmorpholin-2-yl) methoxy) -4-oxobutanoic acid (Reference Example 3) was used.
  • ESI-TOF-MS calculated value: 8270.94 Measured value: 8270.20 [Example 7] PMO. No. 6
  • the title compound was produced in the same manner as in Example 1.
  • the concentration of the extracted total RNA was measured using NanoDrop ND-1000 (manufactured by LMS).
  • One-Step RT-PCR was performed on 400 ng of the extracted total RNA using a Titan One Tube RT-PCR Kit (Roche).
  • a reaction solution was prepared according to the protocol attached to the kit.
  • PTC-100 manufactured by MJ Research
  • the RT-PCR program used is as follows.
  • the base sequences of the forward primer and the reverse primer used in the nested PCR are as follows. 1 ⁇ l of the above-mentioned nested PCR reaction product was analyzed using Bioanalyzer (manufactured by Agilent). The amount of polynucleotide “A” in the band skipped by exon 53 and the amount of polynucleotide “B” in the band not skipped by exon 53 were measured.
  • Skipping efficiency (%) A / (A + B) x 100
  • PMO No. All of the oligomers of the present invention having 1 to 8 are PMO No. It was found that exon 53 was skipped with significantly higher efficiency compared to 11 antisense oligomers.
  • PMO No. The oligomers of the present invention of 3 and 8 are PMO No. Exon skipping efficiency is 4 times higher than 11 antisense oligomers.
  • DMEM F-12 Nutrient Mixture F-12
  • DMEM F-12 fetal calf serum
  • P / S Penicillin / Streptomycin
  • Dulbecco's Modified Eagle Medium Nutrient Mixture F-12 (DMEM F-12) (Invitrogen) did. After 24 hours, the medium was replaced with differentiation medium (DMEM / F-12 containing 2% horse serum (Invitrogen), 1% P / S, and ITS Liquid Media Supplement (Sigma)). The medium was changed every 2 or 3 days and incubated for 12 to 14 days to differentiate into myotube cells.
  • the oligomers of the present invention of 3 and 8 are PMO No. Exon skipping efficiency is more than twice as high as that of 12 antisense oligomers (FIG. 2).
  • PMO No. 3 and 8 to 10 oligomers of the present invention are both available in PMO No. 5 in 5017 cells. It was found that exon 53 was skipped with high efficiency compared to 12 antisense oligomers (FIG. 3).
  • PMO No. The oligomers of the present invention of 3 and 8 are PMO No. Exon skipping efficiency is more than 7 times higher than that of 12 antisense oligomers (FIG. 3).
  • DMEM / F-12 Dulbecco's Modified Eagle Medium: Nutrient Mixture F-12 (DMEM / F-12) (Invitrogen) did. After 24 hours, the medium was replaced with a differentiation medium (DMEM / F-12 containing 2% horse serum (Invitrogen), 1% P / S and ITS Liquid Media Supplement (Sigma)). The medium was changed every two or three days and incubated for 12, 14 or 20 days to differentiate into myotube cells.
  • P / S Penicillin / Streptomycin
  • the oligomers of the present invention of Nos. 3 and 8 are PMO no. It was found that exon 53 was skipped with high efficiency compared to 15 antisense oligomers (FIG. 4).
  • Electrophoresis was performed with NuPAGE Novex Tris-Acetate Gel 3-8% (manufactured by Invitrogen) at 150V for 75 minutes, and transferred to a PVDF membrane (manufactured by Millipore) with a semi-drive lotter. After blocking the PVDF membrane with 5% ECL Blocking Agent (GE Healthcare), the membrane was incubated in an anti-dystrophin antibody (NCL-Dys1, Novokastra) solution. Further, after incubation in a solution of peroxidase-conjugated goat-antimouse IgG (model number, Bio-Rad), color was developed by ECL Plus Western blotting system (manufactured by GE Healthcare). Immunostaining PMO No.
  • oligomers of the present invention were added to the cells, and the cells after 72 hours were fixed in 3% paraformaldehyde for 10 minutes. Incubated with 10% Triton-X for 10 minutes. Blocking with PBS containing 10% goat serum, the membrane was incubated in an anti-dystrophin antibody (NCL-Dys1, Novocastra) solution, and further incubated in an anti-mouse IgG antibody (Invitrogen) solution. Mounted with Pro Long Gold Antifade Reagent (manufactured by Invitrogen) and observed with a fluorescence microscope. Experimental result The results are shown in FIG. 6 and FIG. From this experiment, PMO No. It was confirmed by Western blotting (FIG.
  • RD cells human rhabdomyosarcoma cell line 3 ⁇ 10 5
  • the seeds were seeded in a 6-well plate, Eagle's minimal essential medium (EMEM) medium containing 10% fetal calf serum (FCS) (manufactured by Invitrogen), 2 mL of 37 ° C., 5% in Sigma CO 2 Cultured overnight under conditions.
  • EMEM Eagle's minimal essential medium
  • FCS fetal calf serum
  • FCS fetal calf serum
  • FCS fetal calf serum
  • Various antisense oligomers for exon 53 skipping manufactured by Nippon Bioservice Co., Ltd.
  • Lipofectamine 2000 manufactured by Invitrogen
  • One-Step RT-PCR was performed on 400 ng of the extracted total RNA using a Titan One Tube RT-PCR Kit (Roche). A reaction solution was prepared according to the protocol attached to the kit.
  • the thermal cycler PTC-100 (manufactured by MJ Research) was used.
  • the RT-PCR program used is as follows. 50 ° C, 30 minutes: Reverse transcription reaction 94 ° C, 2 minutes: heat denaturation [94 ° C, 10 seconds; 58 ° C, 30 seconds; 68 ° C, 45 seconds] x 30 cycles: PCR amplification 68 ° C, 7 minutes: Thermal inactivation of polymerase
  • the base sequences of forward primer and reverse primer used for RT-PCR are as follows. Next, nested PCR was performed on the amplification product of the RT-PCR using Taq DNA Polymerase (Roche). The PCR program used is as follows.
  • the base sequences of the forward primer and the reverse primer used in the nested PCR are as follows. 1 ⁇ l of the above-mentioned nested PCR reaction product was analyzed using Bioanalyzer (manufactured by Agilent). The amount of polynucleotide “A” in the band skipped by exon 53 and the amount of polynucleotide “B” in the band not skipped by exon 53 were measured.
  • RD cell human rhabdomyosarcoma cell line
  • 0.3 to 30 ⁇ M of an antisense oligomer was introduced by Nucleofector II (Lonza) using Amaxa Cell Line Nucleofactor Kit L.
  • the program used was T-030. After the introduction, the cells were placed in 2 mL of Eagle's minimal essential medium (EMEM) medium (manufactured by Sigma, the same below) containing 10% fetal calf serum (FCS) (manufactured by Invitrogen) at 37 ° C., 5% CO 2. 2 Cultured overnight under conditions. The cells were washed twice with PBS (manufactured by Nissui, the same applies hereinafter), and then 500 ⁇ l of ISOGEN (manufactured by Nippon Gene) was added to the cells and left at room temperature for several minutes to lyse the cells. It was collected. Total RNA was extracted according to the protocol attached to ISOGEN.
  • EMEM Eagle's minimal essential medium
  • FCS 10% fetal calf serum
  • ISOGEN manufactured by Nippon Gene
  • the concentration of the extracted total RA was measured using NanoDrop ND-1000 (manufactured by LMS).
  • One-Step RT-PCR was performed on 400 ng of the extracted total RNA using QIAGEN OneStep RT-PCR Kit (manufactured by Qiagen).
  • a reaction solution was prepared according to the protocol attached to the kit.
  • PTC-100 manufactured by MJ Research
  • the RT-PCR program used is as follows.
  • the base sequences of forward primer and reverse primer used for RT-PCR are as follows. 1 ⁇ l of the PCR reaction product was analyzed using Bioanalyzer (manufactured by Agilent). The amount of polynucleotide “A” in the band skipped by exon 53 and the amount of polynucleotide “B” in the band not skipped by exon 53 were measured.
  • Skipping efficiency (%) A / (A + B) x 100
  • FIGS. PMO No. No. 8 of the present invention is PMO No. It was found that exon 53 was skipped with significantly higher efficiency compared to 15 and 16 antisense oligomers (FIG. 18). Also, PMO No. The oligomers of the present invention of 3 and 8 are PMO No. It was found that exon 53 was skipped with significantly higher efficiency than the 13 and 14 oligomers of the present invention (FIG. 19). This result shows that skipping efficiency is higher when the 5 ′ end is an —OH group even in the same sequence.
  • the oligomer of the present invention (PMO No. 1 to 10) is remarkably higher in any cellular environment than the oligomer (PMO No. 11, 12, 15 and 16) according to the prior art. It has been shown to skip exon 53 with high efficiency.
  • the 5017 cells used in Test Example 2 are cells collected from DMD patients, and the fibroblasts used in Test Examples 3 and 5 are exon 53 skipping target cells derived from DMD patients.
  • the oligomer of the present invention exhibits an exon 53 skipping efficiency of 90% or more in cells derived from DMD patients to be exon 53 skipped. Therefore, the oligomer of the present invention is actually used in DMD patients. It can be said that exon 53 can be skipped with high efficiency even when administered in the same manner. Therefore, the oligomer of the present invention is very useful in the treatment of DMD.
  • Sequence number 2 Synthetic nucleic acid Sequence number 3: Synthetic nucleic acid Sequence number 4: Synthetic nucleic acid Sequence number 5: Synthetic nucleic acid Sequence number 6: Synthetic nucleic acid Sequence number 7: Synthetic nucleic acid Sequence number 8: Synthetic nucleic acid Sequence number 9: Synthetic nucleic acid Sequence number 10: Synthetic nucleic acid Sequence number 11: Synthetic nucleic acid Sequence number 12: Synthetic nucleic acid Sequence number 13: Synthetic nucleic acid Sequence number 14: Synthetic nucleic acid Sequence number 15: Synthetic nucleic acid Sequence number 16: Synthetic nucleic acid Sequence number 17: Synthetic nucleic acid Sequence number 18: Synthetic nucleic acid SEQ ID NO: 19: Synthetic nucleic acid SEQ ID NO: 20: Synthetic nucleic acid SEQ ID NO: 21: Synthetic nucleic acid SEQ ID NO: 22: Synthetic nucleic acid SEQ ID NO: 23: Synthetic nucleic acid SEQ ID
  • Synthetic nucleic acid SEQ ID NO: 33 Synthetic nucleic acid SEQ ID NO: 34: Synthetic nucleic acid SEQ ID NO: 35: Synthetic nucleic acid SEQ ID NO: 36: Synthetic nucleic acid SEQ ID NO: 37: Synthetic nucleic acid SEQ ID NO: 38: Synthetic nucleic acid SEQ ID NO: 39: Synthetic nucleic acid SEQ ID NO: 40 : Synthetic nucleic acid Sequence number 41: Synthetic nucleic acid Sequence number 42: Synthetic nucleic acid Sequence number 43: Synthetic nucleic acid Sequence number 45: Synthetic nucleic acid Sequence number 46: Synthetic nucleic acid Sequence number 47: Synthetic nucleic acid Sequence number 48: Synthetic nucleic acid Sequence number 49: Synthesis Nucleic acid SEQ ID NO: 50: Synthetic nucleic acid SEQ ID NO: 51: Synthetic nucleic acid SEQ ID NO: 52: Synthetic nucleic acid SEQ ID NO: 53: Synthetic nucleic acid SEQ ID NO
  • Synthetic nucleic acid SEQ ID NO: 59 Synthetic nucleic acid SEQ ID NO: 60: Synthetic nucleic acid SEQ ID NO: 61: Synthetic nucleic acid SEQ ID NO: 62 : Synthetic nucleic acid Sequence number 63: Synthetic nucleic acid Sequence number 64: Synthetic nucleic acid Sequence number 65: Synthetic nucleic acid Sequence number 66: Synthetic nucleic acid Sequence number 67: Synthetic nucleic acid Sequence number 68: Synthetic nucleic acid Sequence number 69: Synthetic nucleic acid Sequence number 70: Synthesis Nucleic acid SEQ ID NO: 71: Synthetic nucleic acid SEQ ID NO: 72: Synthetic nucleic acid SEQ ID NO: 73: Synthetic nucleic acid SEQ ID NO: 74: Synthetic nucleic acid SEQ ID NO: 75: Synthetic nucleic acid SEQ ID NO: 76: Synthetic nucleic acid SEQ ID NO: 77: Synthetic nucleic acid SEQ ID NO

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US20210198306A1 (en) 2021-07-01
CN103154245B (zh) 2016-06-01
JP2023036865A (ja) 2023-03-14
US10487106B2 (en) 2019-11-26
JP2024170458A (ja) 2024-12-10
US20210340171A1 (en) 2021-11-04
EP4403632A2 (en) 2024-07-24
JP6465932B2 (ja) 2019-02-06
JP6867636B1 (ja) 2021-04-28
SMT201900559T1 (it) 2019-11-13
US10407461B2 (en) 2019-09-10
US10870676B2 (en) 2020-12-22
US20200102343A1 (en) 2020-04-02
JP2014054250A (ja) 2014-03-27
RU2013114396A (ru) 2014-10-10
JP5363655B2 (ja) 2013-12-11
JP6647430B2 (ja) 2020-02-14
US20130211062A1 (en) 2013-08-15
ES2750748T3 (es) 2020-03-27
ES2567411T3 (es) 2016-04-22
EP4400168A3 (en) 2024-10-23

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