WO2009020028A1 - Determination and suppression of expression level of g protein-coupled receptor kinase 4 gene in breast cancer cell - Google Patents

Determination and suppression of expression level of g protein-coupled receptor kinase 4 gene in breast cancer cell Download PDF

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Publication number
WO2009020028A1
WO2009020028A1 PCT/JP2008/063701 JP2008063701W WO2009020028A1 WO 2009020028 A1 WO2009020028 A1 WO 2009020028A1 JP 2008063701 W JP2008063701 W JP 2008063701W WO 2009020028 A1 WO2009020028 A1 WO 2009020028A1
Authority
WO
WIPO (PCT)
Prior art keywords
breast cancer
cancer cell
gene
expression level
suppression
Prior art date
Application number
PCT/JP2008/063701
Other languages
French (fr)
Japanese (ja)
Inventor
Masahiko Kuroda
Masakatsu Takanashi
Jun Matsubayashi
Kosuke Oikawa
Masami Tanaka
Original Assignee
Konica Minolta Holdings, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Konica Minolta Holdings, Inc. filed Critical Konica Minolta Holdings, Inc.
Priority to JP2009526409A priority Critical patent/JP4981134B2/en
Publication of WO2009020028A1 publication Critical patent/WO2009020028A1/en

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/57407Specifically defined cancers
    • G01N33/57415Specifically defined cancers of breast
    • 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
    • A61K31/7105Natural ribonucleic acids, i.e. containing only riboses attached to adenine, guanine, cytosine or uracil and having 3'-5' phosphodiester links
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • 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
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/14Type of nucleic acid interfering N.A.
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/158Expression markers

Abstract

It was first discovered that GRK4 is highly expressed in a human breast cancer cell, and it is intended to provide a primer set having specific sequences capable of determining the expression level of a GRK4 gene by PCR, and GRK4 siRNA capable of suppressing human breast cancer cell proliferation. As means for resolution, the sequences of the primer set specific for the GRK4 gene for PCR are represented by SEQ ID NOS: 1 and 2, and the sequences of a double-stranded RNA for siRNA are represented by SEQ ID NOS: 3 to 8.
PCT/JP2008/063701 2007-08-03 2008-07-30 Determination and suppression of expression level of g protein-coupled receptor kinase 4 gene in breast cancer cell WO2009020028A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009526409A JP4981134B2 (en) 2007-08-03 2008-07-30 Quantification and suppression of G protein-coupled receptor kinase 4 gene expression in breast cancer cells

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007203189 2007-08-03
JP2007-203189 2007-08-03

Publications (1)

Publication Number Publication Date
WO2009020028A1 true WO2009020028A1 (en) 2009-02-12

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/063701 WO2009020028A1 (en) 2007-08-03 2008-07-30 Determination and suppression of expression level of g protein-coupled receptor kinase 4 gene in breast cancer cell

Country Status (2)

Country Link
JP (1) JP4981134B2 (en)
WO (1) WO2009020028A1 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004037996A2 (en) * 2002-10-24 2004-05-06 Duke University Evaluation of breast cancer states and outcomes using gene expression profiles
WO2008079269A2 (en) * 2006-12-19 2008-07-03 Genego, Inc. Novel methods for functional analysis of high-throughput experimental data and gene groups identified therfrom

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004037996A2 (en) * 2002-10-24 2004-05-06 Duke University Evaluation of breast cancer states and outcomes using gene expression profiles
WO2008079269A2 (en) * 2006-12-19 2008-07-03 Genego, Inc. Novel methods for functional analysis of high-throughput experimental data and gene groups identified therfrom

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
MATSUBAYASHI J. ET AL.: "DNA Micro Array ni yoru Nyugan no Idenshi Hatsugen Kaiseki", NIHON GAN GAKKAI GAKUJUTSU SOKAI KIJI, vol. 64, 2005, pages 285 + ABSTR. NO. PA2-0624 *
MATSUBAYASHI J. ET AL.: "Nyugan ni Okeru G-protein-coupled receptor kinase 4 no Hatsugen Kaiseki", JOURNAL OF TOKYO MEDICAL COLLEGE, vol. 64, no. 4, 2007, pages 467 - 468 *
PREMONT R.T. ET AL.: "Characterization of the G protein-coupled receptor kinase GRK4. Identification of four splice variants", J. BIOL. CHEM., vol. 271, 1996, pages 6403 - 6410, XP001008847 *
SANADA H. ET AL.: "Amelioration of genetic hypertension by suppression of renal G protein-coupled receptor kinase type 4 expression", HYPERTENSION, vol. 47, 2006, pages 1131 - 1139 *

Also Published As

Publication number Publication date
JPWO2009020028A1 (en) 2010-11-04
JP4981134B2 (en) 2012-07-18

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