CN105264084A - 静默egfr表达的脱氧核糖核酸酶 - Google Patents

静默egfr表达的脱氧核糖核酸酶 Download PDF

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Publication number
CN105264084A
CN105264084A CN201480004837.1A CN201480004837A CN105264084A CN 105264084 A CN105264084 A CN 105264084A CN 201480004837 A CN201480004837 A CN 201480004837A CN 105264084 A CN105264084 A CN 105264084A
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Prior art keywords
oligonucleotide
egfr
sequence
modification sequence
modified
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CN201480004837.1A
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Chinese (zh)
Inventor
杨泮池
赖薇云
白果能
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Academia Sinica
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Academia Sinica
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-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
    • C12N15/1138Non-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 against receptors or cell surface proteins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088Compounds having three or more nucleosides or nucleotides
    • A61K31/713Double-stranded nucleic acids or oligonucleotides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475Growth factors; Growth regulators
    • C07K14/485Epidermal growth factor [EGF], i.e. urogastrone
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/12Type of nucleic acid catalytic nucleic acids, e.g. ribozymes
    • C12N2310/127DNAzymes
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/31Chemical structure of the backbone
    • C12N2310/315Phosphorothioates
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    • C12N2310/33Chemical structure of the base
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/35Nature of the modification
    • C12N2310/351Conjugate
    • C12N2310/3515Lipophilic moiety, e.g. cholesterol
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    • C12N2320/30Special therapeutic applications
    • C12N2320/31Combination therapy
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    • C12N2320/00Applications; Uses
    • C12N2320/30Special therapeutic applications
    • C12N2320/34Allele or polymorphism specific uses

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  • Veterinary Medicine (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
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  • Biotechnology (AREA)
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  • Microbiology (AREA)
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  • Plant Pathology (AREA)
  • Toxicology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)
  • Immunology (AREA)
  • Mycology (AREA)
  • Saccharide Compounds (AREA)
CN201480004837.1A 2013-01-14 2014-01-14 静默egfr表达的脱氧核糖核酸酶 Pending CN105264084A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361752117P 2013-01-14 2013-01-14
US61/752,117 2013-01-14
PCT/US2014/011496 WO2014110577A1 (en) 2013-01-14 2014-01-14 Dnazyme for silencing the expression of egfr

Publications (1)

Publication Number Publication Date
CN105264084A true CN105264084A (zh) 2016-01-20

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ID=51167450

Family Applications (1)

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CN201480004837.1A Pending CN105264084A (zh) 2013-01-14 2014-01-14 静默egfr表达的脱氧核糖核酸酶

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Country Link
US (1) US9856480B2 (enExample)
EP (1) EP2943578B1 (enExample)
JP (1) JP6574136B2 (enExample)
KR (1) KR20150136588A (enExample)
CN (1) CN105264084A (enExample)
CA (1) CA2898200A1 (enExample)
WO (1) WO2014110577A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116286831A (zh) * 2023-01-29 2023-06-23 珠海市人民医院 靶向egfr t790m突变体的核酸适配体及其在制备治疗肺癌药物中的应用

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220061311A1 (en) * 2018-11-05 2022-03-03 The Regents Of The University Of Colorado, A Body Corporate Compositions and methods for reducing cryopreservation toxicity
IL302594A (en) * 2020-11-09 2023-07-01 1E Therapeutics Ltd Catalytic sequence based methods of treating or preventing bacterial infections

Citations (2)

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Publication number Priority date Publication date Assignee Title
WO2004038019A2 (en) * 2002-10-23 2004-05-06 Isis Innovation Limited Dnazyme cleaving mutant polynucleotides
WO2012043633A1 (ja) * 2010-09-30 2012-04-05 独立行政法人国立精神・神経医療研究センター 優性変異遺伝子発現抑制剤

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US20040031072A1 (en) * 1999-05-06 2004-02-12 La Rosa Thomas J. Soy nucleic acid molecules and other molecules associated with transcription plants and uses thereof for plant improvement
US7365185B2 (en) * 2000-07-19 2008-04-29 Monsanto Technology Llc Genomic plant sequences and uses thereof
AU3497701A (en) * 2000-02-08 2001-08-20 Ribozyme Pharmaceuticals, Inc. Nucleozymes with endonuclease activity
EP1767632A3 (en) * 2001-05-29 2009-12-30 Sirna Therpeutics, Inc. A method for local administration of synthetic double-stranded oligonucleotides targeting a VEGF receptor
US6890719B2 (en) * 2002-05-10 2005-05-10 The Board Of Trustess Of The University Of Illinois Fluorescence based biosensor
WO2005108570A1 (ja) * 2004-05-11 2005-11-17 National University Corporation Yokohama National University 核酸酵素複合体
EP1766068A4 (en) * 2004-06-04 2010-03-03 Genentech Inc EGFR Mutations
BRPI0607235A2 (pt) * 2005-02-24 2009-08-25 Amgen Inc mutações do receptor do fator de crescimento epidérmico
CA2683559C (en) 2007-04-13 2019-09-24 Dana Farber Cancer Institute, Inc. Methods for treating cancer resistant to erbb therapeutics

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004038019A2 (en) * 2002-10-23 2004-05-06 Isis Innovation Limited Dnazyme cleaving mutant polynucleotides
WO2012043633A1 (ja) * 2010-09-30 2012-04-05 独立行政法人国立精神・神経医療研究センター 優性変異遺伝子発現抑制剤

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
CRISPIN R. DASS等: "DNAzyme technology and cancer therapy- cleave and let die", 《MOLECULAR CANCER THERAPEUTICS》 *
GANG CHEN等: "Effect of siRNAs targeting the EGFR T790M mutation in a non-small cell lung cancer cell line resistant to EGFR tyrosine kinase inhibitors and combination with various agents", 《BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS》 *
SCOTT K. SILVERMAN: "Catalytic DNA (deoxyribozymes) for synthetic applications-current abilities and future prospects", 《CHEMCOMM》 *
居乃琥: "《酶工程手册》", 31 August 2011, 中国轻工业出版社 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116286831A (zh) * 2023-01-29 2023-06-23 珠海市人民医院 靶向egfr t790m突变体的核酸适配体及其在制备治疗肺癌药物中的应用
CN116286831B (zh) * 2023-01-29 2024-02-20 珠海市人民医院 靶向egfr t790m突变体的核酸适配体及其在制备治疗肺癌药物中的应用

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Publication number Publication date
EP2943578A4 (en) 2017-01-25
WO2014110577A8 (en) 2015-10-08
WO2014110577A1 (en) 2014-07-17
CA2898200A1 (en) 2014-07-17
EP2943578B1 (en) 2019-04-10
JP6574136B2 (ja) 2019-09-18
KR20150136588A (ko) 2015-12-07
US9856480B2 (en) 2018-01-02
JP2016504046A (ja) 2016-02-12
US20160145625A1 (en) 2016-05-26
EP2943578A1 (en) 2015-11-18

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