RU2326691C2 - Использование уреазы для ингибирования роста раковых клеток - Google Patents

Использование уреазы для ингибирования роста раковых клеток Download PDF

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RU2326691C2
RU2326691C2 RU2005104113/15A RU2005104113A RU2326691C2 RU 2326691 C2 RU2326691 C2 RU 2326691C2 RU 2005104113/15 A RU2005104113/15 A RU 2005104113/15A RU 2005104113 A RU2005104113 A RU 2005104113A RU 2326691 C2 RU2326691 C2 RU 2326691C2
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urease
tumor
composition according
enzyme
antitumor
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Герман ЧАО (CA)
Герман ЧАО
Вах ВОНГ (CA)
Вах Вонг
Дональд СЕГАЛ (CA)
Дональд Сегал
Джерри МАКЭЛРОЙ (CA)
Джерри МАКЭЛРОЙ
Джон ДОЧЕРТИ (CA)
Джон Дочерти
Джоди ДИКСТЕЙН (CA)
Джоди Дикстейн
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Хеликс Биофарма Корп.
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Abstract

Данное изобретение относится к медицине и фармакологии и может быть использовано для лечения и диагностики опухолей. Настоящая композиция включает фермент уреазу и нацеливающий фрагмент, непосредственно конъюгированный с уреазой, и опционально слабоосновное противоопухолевое соединение. Изобретение обеспечивает улучшенную доставку фермента к опухолевым клеткам при введении композиции субъекту 2 н. и 4 з.п. ф-лы, 3 табл., 5 ил.

Description

Текст описания приведен в факсимильном виде.
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Claims (6)

1. Фармацевтическая композиция, предназначенная для использования при ингибировании роста опухолевых клеток у млекопитающего-субъекта, включающая фермент уреазу, нацеливающий фрагмент, непосредственно конъюгированный с указанным ферментом уреазой, выбранный из группы, состоящей из антитела к противоопухолевому антигену, антитела к анти-hCG и лиганда, способного к специфическому связыванию с поверхностными рецепторами опухолевых клеток, причем указанный нацеливающий фрагмент способен эффективно усиливать доставку фермента к опухолевым клеткам при введении композиции субъекту и опционально, слабоосновное противоопухолевое соединение, эффективность которого снижается в градиенте более высокого внутриклеточного/более низкого внеклеточного значений рН в солидной опухоли.
2. Композиция по п.1, включающая гибридный белок, состоящий из нацеливающего фрагмента и фермента уреазы.
3. Композиция по п.1, в которой указанная уреаза представляет собой растительную или бактериальную уреазу.
4. Композиция по п.1, в которой противоопухолевое соединение выбирают из группы, состоящей из доксорубицина, даунорубицина, митоксантрона, эпирубицина, митомицина, блеомицина, алкалоидов барвинка (Vinca), таких как винбластин и винкристин, алкилирующих агентов, таких как циклофосфамид и мехлорэтамина гидрохлорид, и противоопухолевых производных пурина и пиримидина.
5. Использование композиции по п.1 в производстве лекарственного средства для лечения или диагностики опухоли у млекопитающего-субъекта.
6. Использование по п.5, в котором противоопухолевое соединение выбирают из группы, состоящей из доксорубицина, даунорубицина, митоксантрона, эпирубицина, митомицина, блеомицина, алкалоидов барвинка (Vinca), таких как винбластин и винкристин, алкилирующих агентов, таких как циклофосфамид и мехлорэтамина гидрохлорид, и противоопухолевых производных пурина и пиримидина.
RU2005104113/15A 2002-07-18 2003-07-16 Использование уреазы для ингибирования роста раковых клеток RU2326691C2 (ru)

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Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7264800B2 (en) * 2002-07-18 2007-09-04 Helix Biopharma Corporation Method and composition for inhibiting cancer cell growth
WO2004023981A2 (en) * 2002-09-11 2004-03-25 Duke University Methods and compositions for blood pool identification, drug distribution quantification and drug release verification
US7769423B2 (en) * 2002-09-11 2010-08-03 Duke University MRI imageable liposomes for the evaluation of treatment efficacy, thermal distribution, and demonstration of dose painting
US20070104732A1 (en) * 2003-10-24 2007-05-10 Bernard Massie Ligand-pseudoreceptor system for generation of adenoviral vectors with altered tropism
IL182956A0 (en) * 2007-05-03 2008-01-20 Yeda Res & Dev Glycan modified soluble receptors and binding proteins and their use
US8892184B2 (en) 2010-10-18 2014-11-18 Siemens Medical Solutions Usa, Inc. Systems and methods for reducing interference in a dual modality imaging system
EP2984170A4 (en) * 2013-04-08 2016-11-30 Helix Biopharma Corp USE OF ANTIBODY UREASE CONJUGATES FOR DIAGNOSTIC AND THERAPEUTIC PURPOSES
KR102318994B1 (ko) * 2015-01-23 2021-10-29 헬릭스 바이오파마 코포레이션 치료학적 목적을 위한 항체-우레아제 접합체
CN110022891A (zh) 2016-09-24 2019-07-16 赫利克斯生物药品公司 恢复肿瘤酸化t细胞的功能
CN110382551A (zh) * 2017-01-05 2019-10-25 赫利克斯生物药品公司 抗vegfr-2脲酶缀合物
WO2021235436A1 (ja) * 2020-05-20 2021-11-25 株式会社メドレックス アポモルヒネ含有経皮吸収型製剤
MX2022015897A (es) * 2020-06-15 2023-01-24 Kortuc Inc Sensibilizador para el tratamiento del cancer.
CN113433087A (zh) * 2021-06-22 2021-09-24 中南大学 一种尿素浓度快速检测方法及检测传感器和应用

Family Cites Families (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4329332A (en) 1978-07-19 1982-05-11 Patrick Couvreur Biodegradable submicroscopic particles containing a biologically active substance and compositions containing them
US4489055A (en) 1978-07-19 1984-12-18 N.V. Sopar S.A. Process for preparing biodegradable submicroscopic particles containing a biologically active substance and their use
US4458066A (en) 1980-02-29 1984-07-03 University Patents, Inc. Process for preparing polynucleotides
FR2504010B1 (fr) 1981-04-15 1985-10-25 Sanofi Sa Medicaments anticancereux contenant la chaine a de la ricine associee a un anticorps antimelanome et procede pour leur preparation
FR2504408B1 (fr) 1981-04-24 1986-02-14 Couvreur Patrick Procede de preparation de particules submicroscopiques, particules ainsi obtenues et compositions pharmaceutiques les contenant
US4671958A (en) 1982-03-09 1987-06-09 Cytogen Corporation Antibody conjugates for the delivery of compounds to target sites
EP0092227B1 (en) 1982-04-19 1988-07-27 Nissan Motor Co., Ltd. Method for controlling reduction ratio of continuously variable transmission with acceleration compensation
US4824783A (en) 1983-12-20 1989-04-25 Enichem S.P.A. Oxidized sulfur derivatives of diaminophosphinyl compounds as urease inhibitors
US4545985A (en) 1984-01-26 1985-10-08 The United States Of America As Represented By The Secretary, Dept. Of Health And Human Services Pseudomonas exotoxin conjugate immunotoxins
US4894443A (en) 1984-02-08 1990-01-16 Cetus Corporation Toxin conjugates
US4625014A (en) 1984-07-10 1986-11-25 Dana-Farber Cancer Institute, Inc. Cell-delivery agent
US4542225A (en) 1984-08-29 1985-09-17 Dana-Farber Cancer Institute, Inc. Acid-cleavable compound
US4659839A (en) 1984-10-10 1987-04-21 Mallinckrodt, Inc. Coupling agents for radiolabeled antibody fragments
ATE66469T1 (de) 1985-01-14 1991-09-15 Neorx Corp Metall-radionuklid markiertes protein fuer diagnose und therapie.
US4837380A (en) * 1985-09-30 1989-06-06 Regents Of University Of California Liposome-calcitonin preparation
US4699784A (en) 1986-02-25 1987-10-13 Center For Molecular Medicine & Immunology Tumoricidal methotrexate-antibody conjugate
US4680333A (en) 1986-04-14 1987-07-14 National Starch And Chemical Corporation Removable hot melt pressure sensitive adhesive
US4867962A (en) 1988-02-26 1989-09-19 Neorx Corporation Functionally specific antibodies
CA1340323C (en) 1988-09-20 1999-01-19 Arnold E. Hampel Rna catalyst for cleaving specific rna sequences
FR2637612B1 (fr) 1988-10-06 1993-09-10 Pasteur Institut Sequences de nucleotides codant pour une proteine a activite ureasique
EP0460607A3 (en) * 1990-06-05 1992-04-01 Bristol-Myers Squibb Company Novel monoclonal antibody to novel antigen associated with human tumors
US5298399A (en) 1990-08-10 1994-03-29 Sapporo Breweries Limited Gene and process for producing a thermostable urease
US5140100A (en) 1990-12-28 1992-08-18 Cedars-Sinai Medical Center Protein that inhibits production of human choriogonadotropin
FR2683159B1 (fr) 1991-10-31 1994-02-25 Coletica Procede de fabrication de nanocapsules a paroi a base de proteines reticulees; nanocapsules ainsi obtenues et compositions cosmetiques, pharmaceutiques et alimentaires en comportant application.
US5573934A (en) * 1992-04-20 1996-11-12 Board Of Regents, The University Of Texas System Gels for encapsulation of biological materials
AU3940293A (en) * 1992-04-03 1993-11-08 Alexander T. YOUNG Gene therapy using targeted viral vectors
US5976535A (en) 1992-06-09 1999-11-02 Neorx Corporation Pretargeting protocols for the enhanced localization of cytotoxins to target sites and cytotoxic combinations useful therefore
US6358490B2 (en) 1992-06-09 2002-03-19 Neorx Corporation Three-step pretargeting methods and compounds
US6290962B1 (en) * 1992-11-03 2001-09-18 Oravax, Inc. Urease-based vaccine and treatment for helicobacter infection
GB9300875D0 (en) 1993-01-18 1993-03-10 Ucb Sa Nanocapsule containing pharmaceutical compositions
CA2151742C (en) 1993-02-22 1999-05-25 Alfred A. Amkraut Compositions for oral delivery of active agents
JPH08509873A (ja) * 1993-05-19 1996-10-22 アンスティテュ・パストゥール ヘリコバクター感染に対する免疫組成物、該組成物に用いられるポリペプチドおよび該ポリペプチドをコードする核酸配列
WO1995031480A1 (en) * 1994-05-18 1995-11-23 S.P.I. Synthetic Peptides Incorporated Heterodimer polypeptide immunogen carrier composition and method
GB9417873D0 (en) 1994-09-06 1994-10-26 Sandoz Ltd Organic compounds
US6172045B1 (en) 1994-12-07 2001-01-09 Neorx Corporation Cluster clearing agents
US5886143A (en) 1994-12-07 1999-03-23 Neorx Corporation Hepatic-directed compounds and reagents for preparation thereof
FR2732605B1 (fr) * 1995-04-07 1997-05-16 Pasteur Merieux Serums Vacc Composition destinee a l'induction d'une reponse immunitaire mucosale
JPH11511979A (ja) * 1995-09-06 1999-10-19 ババリアン・ノルディック・リサーチ・インスティテュート・アクティーゼルスカブ ヒト乳癌細胞を含むヒト乳腺細胞を標的として、連結された異種性遺伝子を発現させるためのwapまたはmmtv制御配列の使用
US6149904A (en) 1996-01-31 2000-11-21 The Regents Of The University Of California Method for inhibiting tumor cell growth by administering to tumor cells expressing a nucleic acid encoding a connexin and a pro-drug
CA2250222A1 (en) 1996-03-20 1997-09-25 Mien-Chie Hung Sensitization of her-2/neu overexpressing cancer cells to chemotherapy
JPH1017492A (ja) * 1996-07-02 1998-01-20 Fuji Yakuhin Kogyo Kk 腫瘍細胞増殖抑制剤
US5958892A (en) 1996-07-30 1999-09-28 Board Of Regents, The University Of Texas System 2-methoxyestradiol-induced apoptosis in cancer cells
US5750496A (en) * 1996-08-12 1998-05-12 Utah State University Method of controlling cryptosporidium infectons using protease inhibitors
EP0824019B1 (en) * 1996-08-13 2002-11-20 Quest International B.V. Inhibition or reduction of oral malodour
EP0932390A1 (en) 1996-10-11 1999-08-04 Sequus Pharmaceuticals, Inc. Therapeutic liposome composition and method
US6261537B1 (en) 1996-10-28 2001-07-17 Nycomed Imaging As Diagnostic/therapeutic agents having microbubbles coupled to one or more vectors
CN1181422A (zh) * 1996-10-31 1998-05-13 上海市肿瘤研究所 与生长因子受体结合的多肽所构建的基因转移载体
US6180114B1 (en) 1996-11-21 2001-01-30 University Of Washington Therapeutic delivery using compounds self-assembled into high axial ratio microstructures
US6045774A (en) 1997-01-10 2000-04-04 Epicyte Pharmaceutical Inc. J chain polypeptide targeting molecule linked to an imaging agent
GB9703633D0 (en) 1997-02-21 1997-04-09 Imp Cancer Res Tech Cancer therapy
US6190923B1 (en) 1997-09-05 2001-02-20 David K. Johnson Diethylenetriamine-N,N′,N″-triacetic acid derivatives
FR2772025B1 (fr) 1997-12-10 2000-03-03 Guerbet Sa Chelates metalliques de macrocycles polyaminocarboxyliques et leur application a l'imagerie par resonance magnetique
US6426086B1 (en) * 1998-02-03 2002-07-30 The Regents Of The University Of California pH-sensitive, serum-stable liposomes
EP1122262B1 (en) * 1998-10-16 2009-12-30 Otsuka Pharmaceutical Co., Ltd. Neovascular-specific peptides
FR2790405B1 (fr) 1999-03-02 2001-04-20 Oreal Nanocapsules a base de polymeres dendritiques
US6300141B1 (en) 1999-03-02 2001-10-09 Helix Biopharma Corporation Card-based biosensor device
US6159443A (en) 1999-04-29 2000-12-12 Vanderbilt University X-ray guided drug delivery
CH694589A5 (de) 1999-06-25 2005-04-15 Genentech Inc Humanisierte Anti-ErbB2-Antikörper und Behandlung mit Anti-ErbB2-Antikörpern.
US6307372B1 (en) 1999-11-02 2001-10-23 Glaxo Wellcome, Inc. Methods for high throughput chemical screening using magnetic resonance imaging
WO2001037721A2 (en) 1999-11-22 2001-05-31 The Research Foundation Of State University Of New York Magnetic nanoparticles for selective therapy
US20020041898A1 (en) 2000-01-05 2002-04-11 Unger Evan C. Novel targeted delivery systems for bioactive agents
WO2002015925A1 (fr) * 2000-08-22 2002-02-28 Kyowa Hakko Kogyo Co., Ltd. Technique de regulation de l'apoptose et polypeptide de regulation d'apoptose
US7148038B2 (en) * 2001-10-16 2006-12-12 Raven Biotechnologies, Inc. Antibodies that bind to cancer-associated antigen CD46 and methods of use thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Shi G et. al "Efficient intracellular drug and gene delivery using folate receptor-targeted pH-sensitive liposomes composed of cationic/anionic lipid combinations.", J Control Release, 2002 Apr. 23; 80(1-3):309-19. Bagshawe KD et. al "A cytotoxic agent can be generated selectively at cancer sites.", Br. J Cancer, 1988 Dec; 58(6):700-3. *

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