DK2741085T3 - Fremgangsmåde til detektering af pancreascancer - Google Patents

Fremgangsmåde til detektering af pancreascancer Download PDF

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DK2741085T3
DK2741085T3 DK12819473.5T DK12819473T DK2741085T3 DK 2741085 T3 DK2741085 T3 DK 2741085T3 DK 12819473 T DK12819473 T DK 12819473T DK 2741085 T3 DK2741085 T3 DK 2741085T3
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Takayoshi Ido
Fumiyoshi Okano
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Toray Industries
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    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574Immunoassay; Biospecific binding assay; Materials therefor for cancer
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    • G01N33/57438Specifically defined cancers of liver, pancreas or kidney
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    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
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    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C07K14/4701Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
    • C07K14/4738Cell cycle regulated proteins, e.g. cyclin, CDC, INK-CCR
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
    • C07K16/303Liver or Pancreas
    • 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
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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    • 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
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/705Assays involving receptors, cell surface antigens or cell surface determinants

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  • Health & Medical Sciences (AREA)
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  • Peptides Or Proteins (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Claims (14)

1. Fremgangsmåde til detektering af pancreascancer, omfattende at måle, i en prøve adskilt fra et individ: (i) tilstedeværelse eller en mængde af et polypeptid med en reaktivitet med specifik binding til et antistof mod et CAPRIN-1-protein via en antigen-antistof-reaktion eller (ii) et antistof mod CAPRIN-1-protein eller (iii) tilstedeværelse eller en mængde af en nukleinsyre, der koder for CAPRIN-1-protein, hvor CAPRIN-1-proteinet består af en aminosyresekvens repræsenteret af et hvilket som helst af SEQ ID Nos: 2 til 30 med lige nummer.
2. Fremgangsmåde ifølge krav 1, hvor polypeptidet er et CAPRIN-1-protein bestående af en aminosyresekvens repræsenteret af et hvilket som helst af SEQ ID NOs: 2 til 30 med lige nummer, eller et polypeptid bestående af en aminosyresekvens med 85-90 % sekvensidentitet eller højere med CAPRIN-1-proteinet.
3. Fremgangsmåde ifølge krav 1 eller 2, hvor individet er et menneske eller en hund.
4. Fremgangsmåde ifølge krav 3, hvor individet er en hund, og CAPRIN-1-proteinet omfatter aminosyresekvensen repræsenteret af SEQ ID NO: 6, 8, 10, 12 eller 14.
5. Fremgangsmåde ifølge krav 3, hvor individet er et menneske, og CAPRIN-1-proteinet omfatter aminosyresekvensen repræsenteret af SEQ ID NO: 2 eller 4.
6. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 5, hvor tilstedeværelsen eller mængden af nukleinsyren i prøven måles under anvendelse af et polynukleotid, der specifikt hybridiserer til en delsekvens omfattende 15-19 eller flere nukleotider eller 20-30 eller flere nukleotider i nukleotidsekvensen af nukleinsyren eller en sekvens, der er komplementær dertil.
7. Fremgangsmåde ifølge krav 6, hvor individet er en hund, og polynukleoti-det specifikt hybridiserer til en delsekvens omfattende 15-19 eller flere nu-kleotider eller 20-30 eller flere nukleotider i nukleotidsekvensen repræsenteret af SEQ ID NO: 5, 7, 9, 11 eller 13 eller en sekvens, der er komplementær dertil.
8. Fremgangsmåde ifølge krav 6, hvor individet er et menneske, og polynu-kleotidet specifikt hybridiserer til en delsekvens omfattende 15-19 eller flere nukleotider eller 20-30 eller flere nukleotider i nukleotidsekvensen repræsenteret af SEQ ID NO: 1 eller 3 eller en sekvens, der er komplementær dertil.
9. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 5, hvor tilstedeværelsen eller mængden af polypeptidet bestemmes ved at måle polypepti-det indeholdt i prøven i et immunologisk assay.
10. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 9, hvor prøven er blod, serum, blodplasma, ascitesvæske, pleuraekssudat, væv eller celler.
11. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 10, hvor antistoffet, der gennemgår en antigen-antistof-reaktion med polypeptidet, er et antistof, der binder til overfladen af en pancreascancercelle.
12. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 11, hvor det antistof, der gennemgår en antigen-antistof-reaktion med polypeptidet, omfatter et antistof med en immunologisk reaktivitet med et polypeptid bestående af en aminosyresekvens omfattende mindst 7 til 12 fortløbende aminosyrere-ster inden for regionen af aminosyrerest Nos. 50 til 98 eller aminosyrerest Nos. 233 til 344 af aminosyresekvensen repræsenteret af et hvilket som helst af SEQ IDS NO: 2 til 30 med lige nummer, bortset fra SEQ ID NOs: 6 og 18.
13. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 12, hvor antistoffet, der gennemgår en antigen-antistof-reaktion med polypeptidet, er et eller flere antistoffer udvalgt fra gruppen bestående af: et antistof, der binder til et polypeptid omfattende aminosyresekvensen repræsenteret af SEQ ID NO: 43; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 44 og 45; et monoklonalt antistof omfattende ami- nosyresekvenserne repræsenteret af SEQ ID NOs: 44 og 46; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 44 og 47; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 44 og 48; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 49 og 50; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 51 og 52; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 53 og 54; et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 55 og 56; et monoklonalt antistof omfattende aminosyresekvensen repræsenteret af SEQ ID NOs: 57 og 58; og et monoklonalt antistof omfattende aminosyresekvenserne repræsenteret af SEQ ID NOs: 59 og 60.
14. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 10, som anvender et reagens eller kit omfattende et eller flere polynukleotider, der specifikt hybridiserer til en delsekvens omfattende 15 til 19 eller flere nukleotider eller 20 til 30 eller flere nukleotider i nukleotidsekvensen repræsenteret af SEQ ID NOs: 1 til 29 med ulige nummer, og som koder for et CAPRIN-1-protein eller i en sekvens, der er komplementær til nukleotidsekvensen.
DK12819473.5T 2011-08-04 2012-08-03 Fremgangsmåde til detektering af pancreascancer DK2741085T3 (da)

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JP2011171364 2011-08-04
PCT/JP2012/069824 WO2013018885A1 (ja) 2011-08-04 2012-08-03 膵臓癌の検出方法

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US (1) US9796775B2 (da)
EP (1) EP2741085B1 (da)
JP (1) JP6094220B2 (da)
KR (1) KR101984554B1 (da)
CN (1) CN103718045B (da)
AU (1) AU2012290948B2 (da)
BR (1) BR112014002616B1 (da)
CA (1) CA2844033C (da)
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ES (1) ES2629061T3 (da)
HU (1) HUE033628T2 (da)
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