CA2402160A1 - Heparinase iii and uses thereof - Google Patents
Heparinase iii and uses thereof Download PDFInfo
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- CA2402160A1 CA2402160A1 CA002402160A CA2402160A CA2402160A1 CA 2402160 A1 CA2402160 A1 CA 2402160A1 CA 002402160 A CA002402160 A CA 002402160A CA 2402160 A CA2402160 A CA 2402160A CA 2402160 A1 CA2402160 A1 CA 2402160A1
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- heparinase iii
- tumor
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- hlgag
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/26—Preparation of nitrogen-containing carbohydrates
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/51—Lyases (4)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/006—Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof
- C08B37/0063—Glycosaminoglycans or mucopolysaccharides, e.g. keratan sulfate; Derivatives thereof, e.g. fucoidan
- C08B37/0075—Heparin; Heparan sulfate; Derivatives thereof, e.g. heparosan; Purification or extraction methods thereof
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/88—Lyases (4.)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/527—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving lyase
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/988—Lyases (4.), e.g. aldolases, heparinase, enolases, fumarase
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
- G01N2500/02—Screening involving studying the effect of compounds C on the interaction between interacting molecules A and B (e.g. A = enzyme and B = substrate for A, or A = receptor and B = ligand for the receptor)
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
- Y10S530/81—Carrier - bound or immobilized peptides or proteins and the preparation thereof, e.g. biological cell or cell fragment as carrier
- Y10S530/811—Peptides or proteins is immobilized on, or in, an inorganic carrier
Abstract
The invention relates to heparinase III and mutants thereof. Modified forms of heparinase III having reduced enzymatic activity which are useful for a variety of purposes, including sequencing of heparin-like glycosaminoglycans (HLGAGs), removing active heparan sulfate from a solution, inhibition of angiogenesis, etc. have been discovered according to the invention. The invention in other aspects relates to methods of treating cancer and inhibiting tumor cell growth and/or metastasis using heparinase III, or products produced by enzymatic cleavage by heparinase III of HLGAGs.
Claims (60)
1. A method for preventing proliferation of a tumor, comprising:
exposing a tumor cell to an effective amount of heparinase III for preventing proliferation of the tumor cells in order to prevent growth of the tumor.
exposing a tumor cell to an effective amount of heparinase III for preventing proliferation of the tumor cells in order to prevent growth of the tumor.
2. The method of claim 1, wherein the heparinase III is a modified heparinase III.
3. The method of claim 1, wherein the heparinase III is a native heparinase III.
4. The method of claim 1, wherein the heparinase III is injected into the tumor in vivo.
5. The method of claim 1, wherein the heparinase III is administered systemically to a subject having a tumor.
6. The method of claim 1, wherein the heparinase III is administered orally to a subject having a tumor.
7. The method of claim 1, wherein the tumor cell is administered the heparinase III in vitro.
8. The method of claim 1, wherein the heparinase III is administered in conjunction with an anti-cancer drug.
9. The method of claim 1, wherein the heparinase III is administered to a subject having a non-metastatic tumor in order to prevent the tumor from becoming metastatic.
10. The method of claim 1, wherein the tumor is selected from the group consisting of a prostate tumor and melanoma.
11. The method of claim 1, wherein the heparinase III is administered to a subject without any additional anti-cancer drugs.
12. A method for preventing tumor cell metastasis, comprising:
exposing a tumor cell to an effective amount of heparinase III for preventing invasion of the tumor cell across a barrier.
exposing a tumor cell to an effective amount of heparinase III for preventing invasion of the tumor cell across a barrier.
13. The method of claim 12, wherein the heparinase III is a modified heparinase III.
14. The method of claim 12, wherein the heparinase III is a native heparinase III.
15. The method of claim 12, wherein the heparinase III is administered in vivo in conjunction with an anti-cancer drug.
16. The method of claim 12, wherein the barrier is an in vivo cell barrier.
17. The method of claim 12, wherein the barrier is an in vitro barrier of an extracellular matrix coated membrane.
18. A method for preparing therapeutic agents for the treatment for a tumor, comprising:
isolating at least a portion of a tumor, treating the portion of the tumor with heparinase III to produce HLGAG
fragments, and isolating the HLGAG fragments, wherein the HLGAG fragment is the therapeutic agent.
isolating at least a portion of a tumor, treating the portion of the tumor with heparinase III to produce HLGAG
fragments, and isolating the HLGAG fragments, wherein the HLGAG fragment is the therapeutic agent.
19. The method of claim 18, further comprising determining the sequence of the HLGAG fragments.
20. A method for treating a subject having a tumor, comprising, administering to the subject a therapeutic HLGAG fragment to treat the tumor.
21. The method of 20, wherein the therapeutic HLGAG fragment administered to the subject is a synthetic HLGAG fragment generated based on the sequence of the HLGAG fragment identified when the tumor is contacted with heparinase III.
22. The method of 20, wherein the therapeutic HLGAG fragment administered to the subject is an isolated HLGAG fragment produced when the tumor is contacted with heparinase III.
23. A composition, comprising:
heparinase III or a therapeutic HLGAG fragment in an effective amount for preventing metastasis of a tumor cell and a targeting molecule for targeting the heparinase III to the tumor, in a pharmaceutically acceptable carrier.
heparinase III or a therapeutic HLGAG fragment in an effective amount for preventing metastasis of a tumor cell and a targeting molecule for targeting the heparinase III to the tumor, in a pharmaceutically acceptable carrier.
24. The composition of claim 23, wherein the heparinase III is a modified heparinase III.
25. The composition of claim 23, wherein the heparinase III is a native heparinase III.
26. The composition of claim 23, wherein the targeting molecule is a compound which binds specifically to an antigen on the surface of a tumor cell.
27. A composition, comprising:
heparinase III or a therapeutic HLGAG fragment in an effective amount for preventing metastasis of a tumor cell and an anti-cancer compound in a pharmaceutically acceptable carrier.
heparinase III or a therapeutic HLGAG fragment in an effective amount for preventing metastasis of a tumor cell and an anti-cancer compound in a pharmaceutically acceptable carrier.
28. A substantially pure heparinase III, comprising:
a polypeptide having the amino acid sequence of the mature peptide of SEQ ID
NO:
2 or having conservative substitutions thereof within residues non-essential to enzymatic function, wherein at least one histidine residue selected from the group consisting of His 36, His105, His110, His139, His152, His225, His234, His241, His424, His469, and His539 has been substituted with a residue selected from the group consisting of alanine, serine, tyrosine, threonine, and lysine.
a polypeptide having the amino acid sequence of the mature peptide of SEQ ID
NO:
2 or having conservative substitutions thereof within residues non-essential to enzymatic function, wherein at least one histidine residue selected from the group consisting of His 36, His105, His110, His139, His152, His225, His234, His241, His424, His469, and His539 has been substituted with a residue selected from the group consisting of alanine, serine, tyrosine, threonine, and lysine.
29. The substantially pure heparinase III of claim 28, wherein the polypeptide has at least one substitution within a histidine residue selected from the group consisting of His110 and His241.
30. The substantially pure heparinase III of claim 28, wherein the polypeptide has a substitution at His110.
31. The substantially pure heparinase III of claim 29, wherein the polypeptide has a substitution at His241.
32. A substantially pure heparinase III comprising:
a modified heparinase III having a modified product profile, wherein the modified product profile of the modified heparinase III is at least 10% different than a native product profile of a native heparinase III.
a modified heparinase III having a modified product profile, wherein the modified product profile of the modified heparinase III is at least 10% different than a native product profile of a native heparinase III.
33. A substantially pure heparinase III comprising:
a modified heparinase III that can cleave a heparan sulfate substrate having a modified heparinase III kcat value, wherein the modified heparinase III kcat value is at least 10% different than a native heparinase III kcat value.
a modified heparinase III that can cleave a heparan sulfate substrate having a modified heparinase III kcat value, wherein the modified heparinase III kcat value is at least 10% different than a native heparinase III kcat value.
34. A pharmaceutical preparation comprising a sterile formulation of the substantially pure heparinase III of any one of claims 28-33 and a pharmaceutically acceptable carrier.
35. An immobilized substantially pure modified heparinase III comprising:
a modified heparinase III as in any one of claims 28-33, and a solid support, wherein the modified heparinase III is immobilized on the solid support.
a modified heparinase III as in any one of claims 28-33, and a solid support, wherein the modified heparinase III is immobilized on the solid support.
36. A method of specifically cleaving a heparin-like glycosaminoglycan, comprising:
contacting a heparin-like glycosaminoglycan with the modified heparinase III
of any one of claims 28, 32, or 33.
contacting a heparin-like glycosaminoglycan with the modified heparinase III
of any one of claims 28, 32, or 33.
37. The method of claim 36, wherein the method is a method of removing active HLGAG fragments from a HLGAG fragment containing fluid.
38. The method of claim 36, wherein the heparinase III is immobilized on a solid support.
39. The method of claim 36, wherein the method is a method for inhibiting angiogenesis and wherein an effective amount for inhibiting angiogenesis of the heparinase III is administered to a subject in need of treatment thereof.
40. The method of claim 36, wherein the heparinase III is administered to a tumor.
41. The method of claim 36, wherein the heparinase III is administered in a biodegradable, biocompatible polymeric delivery device.
42. The method of claim 36, wherein the heparinase III is administered in a pharmaceutically acceptable vehicle for injection.
43. The method of claim 42, wherein the heparinase III is administered in an effective amount for diminishing the number of blood vessels growing into a tumor.
44. The method of claim 36, wherein the heparinase III is administered in a pharmaceutically acceptable vehicle for topical application to the eye.
45. The method of claim 44, wherein the heparinase III is administered in an effective amount for diminishing the symptoms of an eye disease characterized by abnormal neovascularization.
46. The method of claim 36, wherein the heparinase III is administered in a pharmaceutical vehicle suitable for topical application.
47. The method of claim 36, wherein the heparinase III is administered in an effective amount for diminishing the symptoms of psoriasis.
48. The method of claim 36, wherein the method is a method for inhibiting cellular proliferation.
49. The method of claim 36, wherein the method is a method for sequencing HLGAG fragments.
50. A method comprising treating or preventing a subject having a cancer or at risk of developing a cancer by administering to the subject a therapeutic HLGAG
fragment.
fragment.
51. The method of claim 50, wherein the therapeutic HLGAG fragment is a composition of HLGAG fragments wherein at least 50% of the HLGAG fragments are di- or tri- sulfated disaccharides.
52. The method of claim 50, wherein the therapeutic HLGAG fragment is a composition of HLGAG fragments wherein at least 75% of the HLGAG fragments are di- or tri- sulfated disaccharides.
53. The method of claim 50, wherein the therapeutic HLGAG fragment is a composition of HLGAG fragments wherein at least 90% of the HLGAG fragments are di- or tri- sulfated disaccharides.
54. The method of claim 50, wherein the therapeutic HLGAG fragment is free of mono- or un- sulfated disaccharides.
55. A method for preparing LMWH, comprising:
contacting an HLGAG sample with a modified heparinase III molecule to produce LMWH.
contacting an HLGAG sample with a modified heparinase III molecule to produce LMWH.
56. A composition, comprising, the LMWH produced by the method of claim 55.
57. A method for treating or preventing a disorder associated with coagulation, comprising:
administering to a subject an effective amount of the composition of claim 56 to treat or prevent a disorder associated with coagulation.
administering to a subject an effective amount of the composition of claim 56 to treat or prevent a disorder associated with coagulation.
58. A method for treating or preventing a tumor, comprising:
administering to a subject an effective amount of the composition of claim 56 to treat or prevent a tumor in the subject.
administering to a subject an effective amount of the composition of claim 56 to treat or prevent a tumor in the subject.
59. A method for treating or preventing psoriasis, comprising:
administering to a subject an effective amount of the composition of claim 56 to treat or prevent psoriasis in the subject.
administering to a subject an effective amount of the composition of claim 56 to treat or prevent psoriasis in the subject.
60. A method for treating or preventing neovascularization, comprising:
administering to a subject an effective amount of the composition of claim 56 to treat or prevent neovascularization in the subject.
administering to a subject an effective amount of the composition of claim 56 to treat or prevent neovascularization in the subject.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18784600P | 2000-03-08 | 2000-03-08 | |
US60/187,846 | 2000-03-08 | ||
PCT/US2001/007464 WO2001066772A2 (en) | 2000-03-08 | 2001-03-08 | Heparinase iii and uses thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2402160A1 true CA2402160A1 (en) | 2001-09-13 |
CA2402160C CA2402160C (en) | 2012-02-14 |
Family
ID=22690719
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2402160A Expired - Lifetime CA2402160C (en) | 2000-03-08 | 2001-03-08 | Heparinase iii and uses thereof |
Country Status (7)
Country | Link |
---|---|
US (8) | US6869789B2 (en) |
EP (1) | EP1266013B1 (en) |
JP (1) | JP2003525946A (en) |
AU (2) | AU2001243512C1 (en) |
CA (1) | CA2402160C (en) |
ES (1) | ES2527853T3 (en) |
WO (1) | WO2001066772A2 (en) |
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-
2001
- 2001-03-08 JP JP2001565375A patent/JP2003525946A/en active Pending
- 2001-03-08 EP EP01916493.8A patent/EP1266013B1/en not_active Expired - Lifetime
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- 2001-03-08 US US09/802,285 patent/US6869789B2/en not_active Expired - Lifetime
- 2001-03-08 AU AU4351201A patent/AU4351201A/en active Pending
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2002
- 2002-11-08 US US10/291,337 patent/US20030099628A1/en not_active Abandoned
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AU2001243512C1 (en) | 2008-04-17 |
AU2001243512B2 (en) | 2007-05-10 |
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WO2001066772A2 (en) | 2001-09-13 |
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US7390633B2 (en) | 2008-06-24 |
US6869789B2 (en) | 2005-03-22 |
JP2003525946A (en) | 2003-09-02 |
EP1266013B1 (en) | 2014-10-15 |
US20060067928A1 (en) | 2006-03-30 |
US20020122793A1 (en) | 2002-09-05 |
US20050233402A1 (en) | 2005-10-20 |
US20060182734A1 (en) | 2006-08-17 |
ES2527853T3 (en) | 2015-01-30 |
US20030099628A1 (en) | 2003-05-29 |
EP1266013A2 (en) | 2002-12-18 |
CA2402160C (en) | 2012-02-14 |
US20060183713A1 (en) | 2006-08-17 |
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