Angiogenic compounds and uses thereof

• US 20060014727A1
• Filed: 06/20/2005
• Published: 01/19/2006
• Est. Priority Date: 12/24/2002
• Status: Abandoned Application

• Current Assignee: University of British Columbia
• Original Assignee: University of British Columbia
• Inventors: Andersen, Raymond, Roberge, Michel, Karsan, Aly, Pollet, Ingrid
• Application Number:
  US11/158,291
• Publication Number:
  US 20060014727A1
• Time in Patent Office: Days
• US Class Current: 514/169
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 31/575 substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
• CPC Class Codes: A61K 38/1825 Fibroblast growth factor [FGF]
• CPC Class Codes: A61K 38/1866 Vascular endothelial growth factor [VEGF]
• CPC Class Codes: C07J 31/00 Normal steroids containing one or more sulfur atoms not belonging to a hetero ring
• CPC Class Codes: C07J 31/006 not covered by C07J31/003
• CPC Class Codes: G01N 33/5008 for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
• CPC Class Codes: G01N 33/5017 for testing neoplastic activity
• CPC Class Codes: G01N 33/5026 on cell morphology
• CPC Class Codes: G01N 33/5064 Endothelial cells

Abstract

The invention provides sterol sulphate compounds and compositions that are capable of promoting angiogenesis. The invention also provides methods and uses for these compounds.

Claims

1. A compound of Formula I or a salt thereof,

wherein

R is a linear or branched, saturated or unsaturated one to 15 carbon alkyl group;

X, Y, and Z are independently selected from the group consisting of H, OH, and OSO₃⁻

; and

at least one of X, Y, or Z is OSO₃⁻

;

provided that the compound does not have the precise structure of any of the structures listed in Tables I or II.

2. The compound of claim 1, wherein the combination of X, Y, and Z is selected from the group consisting of where X and Y are sulphate, Z is H or OH;

X and Z are sulphate, Y is H or OH;

Y and Z are sulphate, X is H or OH;

X is sulphate, Y and Z are H or OH;

Y is sulphate, X and Z are H or OH; and

Z is sulphate, X and Y are H or OH.

3. The compound of claim 1, wherein X, Y, and Z are all sulphate (OSO₃.

4. The compound of claim 1, wherein R comprises the side chain of sokotrasterol sulphate.

5. The compound of claim 1, wherein R is not the precise side chain of cholesterol.

6. The compound of claim 1, wherein the compound is substantially pure.

10. The pharmaceutical composition of claim 7, comprising a compound according to claim 1.

7. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and one or more compounds of Formula I or pharmaceutically acceptable salts thereof,

wherein

R is a linear or branched, saturated or unsaturated one to 15 carbon alkyl group;

X, Y, and Z are independently selected from the group consisting of H, OH, and OSO₃⁻

; and

at least one of X, Y, or Z is OSO₃⁻

.

8. The pharmaceutical composition of claim 7, wherein the one or more compounds of Formula I is not solely a compound listed in Table I.

9. The pharmaceutical composition of claim 7, comprising sokotrasterol sulphate.

11. The pharmaceutical composition of claim 7, comprising a compound listed in Table II.

12. The pharmaceutical composition of claim 7, further comprising vascular endothelial growth factor or fibroblast growth factor 2.

13. The pharmaceutical composition of claim 7, wherein the pharmaceutical composition is capable of promoting angiogenesis.

14. The pharmaceutical composition of claim 13, wherein the promotion of angiogenesis is in the chorioallantoic membrane of chick embryo.

15. The pharmaceutical composition of claim 7, wherein the pharmaceutical composition is capable of promoting endothelial cell proliferation or sprouting.

16. The pharmaceutical composition of claim 7, wherein the pharmaceutical composition is capable of treating or preventing a disorder associated with sub-optimal angiogenesis.

17. The pharmaceutical composition of claim 16, wherein the disorder is selected from the group consisting of ischemia, circulatory disorders, vascular disorders, myocardial disease, pericardial disease, congenital heart disease, peripheral vascular pathologies, diabetes, coronary artery disease, atherosclerosis, infertility, insufficient endometrial vascularization, occluded blood vessels, conditions involving the pathology of endothelial cells, peptic ulcerations, endothelial ulcerations, restenosis, and wounds.

18. The pharmaceutical composition of claim 17, wherein the ischemia is selected from the group consisting of ischemic stroke, cerebral ischemia, myocardial ischemia, intestinal ischemia, retinal or ocular ischemia, and spinal ischemia.

19. A method of treatment or prophylaxis of a disorder associated with sub-optimal angiogenesis, comprising administering to a subject in need thereof an effective amount of a pharmaceutical composition of claim 7.

20. A method of promoting angiogenesis or promoting proliferation or sprouting of endothelial cells, comprising administering an amount of one or more compounds of Formula I or pharmaceutically acceptable salts thereof,

wherein

R is a linear or branched, saturated or unsaturated one to 15 carbon alkyl group;

X, Y, and Z are independently selected from the group consisting of H, OH, and OSO₃⁻

; and

at least one of X, Y, or Z is OSO₃⁻

, and

wherein said amount is sufficient to promote angiogenesis or to promote proliferation or sprouting of endothelial cells.

21. The method of claim 20, wherein said compound is sokotrasterol sulphate.

22. The method of claim 20, wherein said compound is a compound listed in Tables I or II.

23. The method of claim 20, wherein the promotion of angiogenesis is in the chorioallantoic membrane of chick embryo.

24. The method of claim 20, wherein the subject is a human.

25. The method of claim 20, wherein the method is carried out in vivo or in vitro.

26. A method of treating or preventing a disorder associated with sub-optimal angiogenesis, comprising administering an effective amount of one or more compounds of Formula I or pharmaceutically acceptable salts thereof,

wherein

R is a linear or branched, saturated or unsaturated one to 15 carbon alkyl group;

X, Y, and Z are independently selected from the group consisting of H, OH, and OSO₃⁻

; and

at least one of X, Y, or Z is OSO₃⁻

; and

wherein said amount is sufficient to treat or prevent the disorder associated with sub-optimal angiogenesis.

27. The method of claim 26, wherein said compound is sokotrasterol sulphate.

28. The method of claim 26, wherein said compound is a compound listed in Tables I or II.

29. The method of claim 26, wherein the disorder is selected from the group consisting of ischemia, circulatory disorders, vascular disorders, myocardial disease, pericardial disease, congenital heart disease, peripheral vascular pathologies, diabetes, coronary artery disease, atherosclerosis, infertility, insufficient endometrial vascularization, occluded blood vessels, conditions involving the pathology of endothelial cells, peptic ulcerations, endothelial ulcerations, restenosis, and wounds.

30. The method of claim 29, wherein the ischemia is selected from the group consisting of ischemic stroke, cerebral ischemia, myocardial ischemia, intestinal ischemia, retinal or ocular ischemia, and spinal ischemia.

31. The method of claim 26, wherein the subject is a human.

32. The method of claim 26, wherein the method is carried out in vivo or in vitro.

33. A method of identifying a sterol sulphate compound that is capable of promoting angiogenesis, the method comprising screening the compound for activity in promoting angiogenesis.

34. The method of claim 33, comprising

a) contacting the chorioallantoic membrane of a first group of chick embryos with the compound;

b) contacting the chorioallantoic membrane of a second group of chick embryos with a composition lacking the compound;

c) determining the angiogenic response of the first and second groups of chick embryos; and

d) selecting a compound that increases the angiogenic response in the first group of chick embryos compared to the second group of chick embryos by at least 10%.

35. The method of claim 33, comprising

a) contacting a first group of endothelial cells with the compound;

b) contacting a second group of endothelial cells with a composition lacking the compound;

c) determining the angiogenic response of the first and second groups of endothelial cells; and

d) selecting a compound that increases the angiogenic response in the first group of endothelial cells as compared to the second group of endothelial cells by at least 10%.

36. The method of claim 35, wherein the endothelial cells are human umbilical vein endothelial cells.

37. The method of claim 34, wherein the angiogenic response is determined by determining the sprouting of the endothelial cells.

38. The method of claim 33, wherein the compound has the chemical structure of Formula I or pharmaceutically acceptable salts thereof,

wherein

R is a linear or branched, saturated or unsaturated one to 15 carbon alkyl group;

X, Y, and Z are independently selected from the group consisting of H, OH, and OSO₃⁻

; and

t least one of X, Y, or Z is OSO₃⁻

.