WO2015060736A3 - The use of egfr and hgfr agonists as anticancer drugs acting on tumour cells of certain phenotype - Google Patents

The use of egfr and hgfr agonists as anticancer drugs acting on tumour cells of certain phenotype Download PDF

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Publication number
WO2015060736A3
WO2015060736A3 PCT/PL2014/000115 PL2014000115W WO2015060736A3 WO 2015060736 A3 WO2015060736 A3 WO 2015060736A3 PL 2014000115 W PL2014000115 W PL 2014000115W WO 2015060736 A3 WO2015060736 A3 WO 2015060736A3
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WO
WIPO (PCT)
Prior art keywords
egfr
hgfr
agonists
mutakthet
mutant
Prior art date
Application number
PCT/PL2014/000115
Other languages
French (fr)
Other versions
WO2015060736A2 (en
Inventor
Piotr Rieske
Ewelina STOCZYŃSKA-FIDELUS
Sylwester Piaskowski
Cezary TRĘDA
Maiej WALCZAK
Dawid Grzela
Andrzej WYRZYKOWSKI
Original Assignee
Celther Polska Sp. Z.O.O.
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 Celther Polska Sp. Z.O.O. filed Critical Celther Polska Sp. Z.O.O.
Publication of WO2015060736A2 publication Critical patent/WO2015060736A2/en
Publication of WO2015060736A3 publication Critical patent/WO2015060736A3/en

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    • 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
    • C07K14/475Growth factors; Growth regulators
    • C07K14/485Epidermal growth factor [EGF], i.e. urogastrone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18Growth factors; Growth regulators
    • A61K38/1808Epidermal growth factor [EGF] urogastrone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18Growth factors; Growth regulators
    • A61K38/1833Hepatocyte growth factor; Scatter factor; Tumor cytotoxic factor II
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18Growth factors; Growth regulators
    • A61K38/1841Transforming growth factor [TGF]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07K14/475Growth factors; Growth regulators
    • C07K14/4753Hepatocyte growth factor; Scatter factor; Tumor cytotoxic factor II

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Gastroenterology & Hepatology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Zoology (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Genetics & Genomics (AREA)
  • Toxicology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (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 Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Current opinion is that anti-carcinogenic effects related to receptors such as EGFR or HGFR (MET) and their mutants may be achieved by means of blocking them. Though, there are situations in which anti-carcinogenic therapy may be based on activation of these receptors. Condition, under which the EGFR agonists exert their anti-carcinogenic effects is that cells treated with them should present high expression levels of activating heterodimerization-inducing EGFR mutant (EGFRMUTaktHET) and EGFRwt. Similarly, high expression level of HGFR and the activating heterodimerization-inducing EGFR mutant is possible. Anti-carcinogenic effects of EGFR agonists are also possible in cells showing over-expression of EGFR only, without increased level of the EGFR mutant (EGFRMUTaktHET), as well as anti-carcinogenic effects of HGFR agonists can be observed in cells showing over-expression of HGFR only, without increased level of the EGFR mutant (EGFRMUTaktHET).
PCT/PL2014/000115 2013-10-24 2014-10-23 The use of egfr and hgfr agonists as anticancer drugs acting on tumour cells of certain phenotype WO2015060736A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PLPL405768 2013-10-24
PL40576813A PL405768A1 (en) 2013-10-24 2013-10-24 Application of EGFR and HGFR agonists as anticancer drugs, acting on cancer cells with specified phenotype

Publications (2)

Publication Number Publication Date
WO2015060736A2 WO2015060736A2 (en) 2015-04-30
WO2015060736A3 true WO2015060736A3 (en) 2015-07-30

Family

ID=51999483

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/PL2014/000115 WO2015060736A2 (en) 2013-10-24 2014-10-23 The use of egfr and hgfr agonists as anticancer drugs acting on tumour cells of certain phenotype

Country Status (2)

Country Link
PL (1) PL405768A1 (en)
WO (1) WO2015060736A2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111254117B (en) * 2018-11-30 2022-05-31 中国科学院大连化学物理研究所 Mutant EGFR high-expression recombinant MHCC97-L liver cancer cell and construction

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001009186A2 (en) * 1999-07-30 2001-02-08 Medarex, Inc. Therapeutic compounds comprised of anti-fc receptor binding agents
WO2006038880A1 (en) * 2004-10-08 2006-04-13 Damavand'wound Ab New composition and method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001009186A2 (en) * 1999-07-30 2001-02-08 Medarex, Inc. Therapeutic compounds comprised of anti-fc receptor binding agents
WO2006038880A1 (en) * 2004-10-08 2006-04-13 Damavand'wound Ab New composition and method

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
D. W. BARNES: "Epidermal growth factor inhibits growth of A431 human epidermoid carcinoma in serum-free cell culture", THE JOURNAL OF CELL BIOLOGY, vol. 93, no. 1, 1 April 1982 (1982-04-01), pages 1 - 4, XP055181212, ISSN: 0021-9525, DOI: 10.1083/jcb.93.1.1 *
JOHNS TERRANCE G ET AL: "The efficacy of epidermal growth factor receptor-specific antibodies against glioma xenografts is influenced by receptor levels, activation status, and heterodimerization", CLINICAL CANCER RESEARCH, THE AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 13, no. 6, 15 March 2007 (2007-03-15), pages 1911 - 1925, XP002614294, ISSN: 1078-0432, DOI: 10.1158/1078-0432.CCR-06-1453 *

Also Published As

Publication number Publication date
PL405768A1 (en) 2015-04-27
WO2015060736A2 (en) 2015-04-30

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