CA2553436A1 - Peptides selectivement letaux pour des cellules mammiferes transformees et malignes - Google Patents

Peptides selectivement letaux pour des cellules mammiferes transformees et malignes Download PDF

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Publication number
CA2553436A1
CA2553436A1 CA002553436A CA2553436A CA2553436A1 CA 2553436 A1 CA2553436 A1 CA 2553436A1 CA 002553436 A CA002553436 A CA 002553436A CA 2553436 A CA2553436 A CA 2553436A CA 2553436 A1 CA2553436 A1 CA 2553436A1
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Canada
Prior art keywords
peptide
seq
derivative
analog
cells
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
CA002553436A
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English (en)
Inventor
Matthew R. Pincus
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Research Foundation of State University of New York
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Individual
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
Priority claimed from PCT/US2004/000684 external-priority patent/WO2004081030A2/fr
Application filed by Individual filed Critical Individual
Publication of CA2553436A1 publication Critical patent/CA2553436A1/fr
Abandoned legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • 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
    • C07K14/46Peptides 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
    • C07K14/4746Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used p53
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • G01N33/5005Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/5011Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing antineoplastic activity
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/01Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/10Fusion polypeptide containing a localisation/targetting motif containing a tag for extracellular membrane crossing, e.g. TAT or VP22

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Urology & Nephrology (AREA)
  • Medicinal Chemistry (AREA)
  • Hematology (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Biochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Biotechnology (AREA)
  • Food Science & Technology (AREA)
  • Analytical Chemistry (AREA)
  • Toxicology (AREA)
  • Microbiology (AREA)
  • General Physics & Mathematics (AREA)
  • Cell Biology (AREA)
  • Pathology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Zoology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Hospice & Palliative Care (AREA)
  • Oncology (AREA)
  • Peptides Or Proteins (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

L'invention concerne des peptides correspondant à la totalité ou à une partie de résidus d'acide aminé 12-26 de la protéine p53. Ces peptides sont létaux pour des cellules transformées et malignes, lorsqu'ils sont fusionnés à une séquence de tête de pénétration membranaire. Pour réduire la protéolyse d'un tel peptide, au moins un acide aminé D peut être substitué par des acides aminés L correspondants de la partie p53 et/ou de la tête de pénétration membranaire du peptide. En outre, une liaison pseudopepditique ou une liaison pseudopeptidique rétro/inverso peut être substituée par au moins une liaison peptidique dans la séquence p53 ou dans la séquence de tête de pénétration membranaire, ou dans les deux, de sorte à rendre le peptide susmentionné moins prédisposé à une protéolyse. En outre, à la fois la séquence de tête de pénétration membranaire et la partie p53 du peptide susmentionné peuvent comprendre des isomères rétro/inverso et des isomères rétro/inverso partiellement modifiés. De tels isomères sont moins sensibles à une protéolyse, et présentent par conséquent des demi-vies prolongées. Les peptides susmentionnés sont utiles pour traiter une maladie néoplastique chez un animal, de préférence un humain. L'invention concerne des compositions pharmaceutiques comprenant les peptides susmentionnés mélangés à un excipient pharmaceutiquement acceptable. L'invention concerne des méthodes de traitement d'une maladie néoplastique chez un patient. Ces méthodes consistent à administrer un peptide susmentionné fusionné à son extrémité carboxyterminale à une séquence de tête de pénétration membranaire. L'invention concerne également des méthodes pour évaluer le niveau d'efficacité d'un peptide susmentionné pour tuer in vitro des cellules néoplastiques ou des cellules transformées ou des cellules malignes.
CA002553436A 2004-01-13 2004-12-22 Peptides selectivement letaux pour des cellules mammiferes transformees et malignes Abandoned CA2553436A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
USPCT/US2004/000684 2004-01-13
PCT/US2004/000684 WO2004081030A2 (fr) 2003-03-12 2004-01-13 Peptides selectivement letaux pour les cellules malignes et transformees
PCT/US2004/044073 WO2006006954A2 (fr) 2004-01-13 2004-12-22 Peptides selectivement letaux pour des cellules mammiferes transformees et malignes

Publications (1)

Publication Number Publication Date
CA2553436A1 true CA2553436A1 (fr) 2006-01-19

Family

ID=35784274

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002553436A Abandoned CA2553436A1 (fr) 2004-01-13 2004-12-22 Peptides selectivement letaux pour des cellules mammiferes transformees et malignes

Country Status (5)

Country Link
EP (1) EP1706419A2 (fr)
JP (1) JP2008505846A (fr)
AU (1) AU2004321478A1 (fr)
CA (1) CA2553436A1 (fr)
WO (1) WO2006006954A2 (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1490089A4 (fr) * 2002-03-12 2006-08-30 Univ New York State Res Found Peptides selectivement letaux pour des cellules de mammiferes transformees et malignes

Also Published As

Publication number Publication date
AU2004321478A1 (en) 2006-01-19
WO2006006954A3 (fr) 2006-07-13
EP1706419A2 (fr) 2006-10-04
WO2006006954A2 (fr) 2006-01-19
JP2008505846A (ja) 2008-02-28

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Legal Events

Date Code Title Description
FZDE Discontinued
FZDE Discontinued

Effective date: 20081222