Methods of using thrombin derivatives to treat medulloblastoma
Provided herein are methods for using a thrombin peptide derivative to treat a medulloblastoma. In one embodiment, the method includes administering to a subject having a medulloblastoma an effective amount of a thrombin peptide derivative, and exposing cells of the medulloblastoma of the subject to a cancer treatment after administering the thrombin peptide derivative to the subject. An example of a cancer treatment is radiation therapy. In one embodiment, viability of cells of the medulloblastoma is decreased compared to viability of cells of the medulloblastoma before the administering and the exposing. The cells of the medulloblastoma having decreased viability can be cancer stem cells. In one embodiment, shrinkage of the medulloblastoma in the subject is increased compared to shrinkage of the medulloblastoma before the administering and the exposing.
1. A method comprising:
administering to a subject having a medulloblastoma an effective amount of a thrombin peptide derivative, wherein the thrombin peptide derivative comprises Asp-Ala-R, wherein R is a serine esterase conserved sequence, and wherein the serine esterase conserved sequence comprises the sequence Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:15), wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val; and
exposing cells of the medulloblastoma of the subject to a therapeutic radiation,
wherein the thrombin peptide derivative is administered before the therapeutic radiation,
wherein the thrombin peptide derivative is administered between 1 hour and 60 hours before the exposing;
and wherein viability of cells of the medulloblastoma is decreased compared to viability of cells of the medulloblastoma before the administering and the exposing.
2. The method of claim 1 wherein the cells of the medulloblastoma having decreased viability comprise cancer stem cells.
3. The method of claim 1 wherein the administration is systemic.
4. The method of claim 3 wherein the systemic administration is intravenous.
5. The method of claim 1 wherein the subject is a child or young adult.
6. The method of claim 1 wherein the medulloblastoma is a relapse following an initial treatment.
7. The method of claim 1 wherein the thrombin peptide derivative comprises the sequence Arg-Gly-Asp-Ala-Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:1), wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val.
8. The method of claim 1 wherein the thrombin peptide derivative comprises the sequence Ala-Gly-Tyr-Lys-Pro-Asp-Glu-Gly-Lys-Arg-Gly-Asp-Ala-Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:2), an N-terminal truncated fragment thereof comprising at least fourteen amino acid residues, wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val.
9. The method of claim 1 wherein the thrombin peptide derivative is H-Ala-Gly-Tyr-Lys-Pro-Asp-Glu-Gly-Lys-Arg-Gly-Asp-Ala-Cys-Glu-Gly-Asp-Ser-Gly-Gly-Pro-Phe-Val-NH 2 (SEQ ID NO:3).
10. A method of comprising:
administering to a subject having a medulloblastoma an effective amount of a thrombin peptide derivative, wherein the thrombin peptide derivative comprises the polypeptide Arg-Gly-Asp-Ala-Xaa-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:4), wherein Xaa is alanine, glycine, serine or an S-protected cysteine; X 1 is Glu or Gln; and X 2 is Phe, Met, Leu, His or Val; and
exposing cells of the medulloblastoma of the subject to a therapeutic radiation,
wherein the thrombin peptide derivative is administered before the therapeutic radiation,
wherein the thrombin peptide derivative is administered between 1 hour and 60 hours before the exposing;
and wherein viability of cells of the medulloblastoma is decreased compared to viability of cells of the medulloblastoma before the administering and the exposing.
11. The method of claim 1 wherein the thrombin derivative comprises a C-terminal amide, an acylated N-terminus, or a combination thereof, wherein said C-terminal amide is represented by —C(O)NR a R b , wherein R a and R b are independently hydrogen, an aliphatic group comprising up to 10 carbon atoms, or R a and R b , taken together with the nitrogen to which they are bonded, form a C 3 -C 10 non-aromatic heterocyclic group, and wherein said N-terminal acyl group is represented by R c C(O)—, where R c is hydrogen, an aliphatic group comprising up to 10 carbon atoms or a phenyl group optionally substituted with one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, nitro and cyano.
12. A method comprising:
administering to a subject having a medulloblastoma an effective amount of a thrombin peptide derivative, wherein the thrombin peptide derivative comprises Asp-Ala-R, wherein R is a serine esterase conserved sequence, and wherein the serine esterase conserved sequence comprises the sequence Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:15), wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val; and
exposing cells of the medulloblastoma of the subject to a therapeutic radiation,
wherein the thrombin peptide derivative is administered before the therapeutic radiation,
wherein the thrombin peptide derivative is administered between 1 hour and 60 hours before the exposing;
and wherein shrinkage of the medulloblastoma in the subject is increased compared to shrinkage of the medulloblastoma before the administrating and the exposing.
13. The method of claim 12 wherein the administration is systemic.
14. The method of claim 13 wherein the systemic administration is intravenous.
15. The method of claim 12 wherein the subject is a child or young adult.
16. The method of claim 12 wherein the medulloblastoma is a relapse following an initial treatment.
17. The method of claim 12 wherein the thrombin peptide derivative comprises the sequence Arg-Gly-Asp-Ala-Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:1), wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val.
18. The method of claim 12 wherein the thrombin peptide derivative comprises the sequence Ala-Gly-Tyr-Lys-Pro-Asp-Glu-Gly-Lys-Arg-Gly-Asp-Ala-Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:2), an N-terminal truncated fragment thereof comprising at least fourteen amino acid residues, wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val.
19. The method of claim 12 wherein the thrombin peptide derivative is H-Ala-Gly-Tyr-Lys-Pro-Asp-Glu-Gly-Lys-Arg-Gly-Asp-Ala-Cys-Glu-Gly-Asp-Ser-Gly-Gly-Pro-Phe-Val-NH 2 (SEQ ID NO:3).
20. A method comprising:
administering to a subject having a medulloblastoma an effective amount of a thrombin peptide derivative, wherein the thrombin peptide derivative comprises the polypeptide Arg-Gly-Asp-Ala-Xaa-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:4), wherein Xaa is alanine, glycine, serine or an S-protected cysteine; X 1 is Glu or Gln; and X 2 is Phe, Met, Leu, His or Val; and
exposing cells of the medulloblastoma of the subject to a therapeutic radiation,
wherein the thrombin peptide derivative is administered before the therapeutic radiation
wherein the thrombin peptide derivative is administered between 1 hour and 60 hours before the exposing;
and wherein shrinkage of the medulloblastoma in the subject is increased compared to shrinkage of the medulloblastoma before the administrating and the exposing.
21. The method of claim 12 wherein the thrombin derivative comprises a C-terminal amide, an acylated N-terminus, or a combination thereof, wherein said C-terminal amide is represented by —C(O)NR a R b , wherein R a and R b are independently hydrogen, an aliphatic group comprising up to 10 carbon atoms, or R a and R b , taken together with the nitrogen to which they are bonded, form a C 3 -C 10 non-aromatic heterocyclic group, and wherein said N-terminal acyl group is represented by R c C(O)—, where R c is hydrogen, an aliphatic group comprising up to 10 carbon atoms or a phenyl group optionally substituted with one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, nitro and cyano.
22. A method comprising:
contacting a medulloblastoma cancer cell with an effective amount of a thrombin peptide derivative, wherein the thrombin peptide derivative comprises Asp-Ala-R, wherein R is a serine esterase conserved sequence, and wherein the serine esterase conserved sequence comprises the sequence Cys-X 1 -Gly- Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:15), wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val; and
exposing the medulloblastoma cancer cell to a therapeutic radiation,
wherein the medulloblastoma cancer cell is contacted with the thrombin peptide derivative before the radiation,
wherein the thrombin peptide derivative is administered between 1 hour and 60 hours before the exposing;
and wherein the viability of the medulloblastoma cancer cell is decreased compared to the viability of the medulloblastoma cancer before the contacting and exposing.
23. The method of claim 22 wherein the medulloblastoma cancer cell is ex vivo.
24. The method of claim 22 wherein the thrombin peptide derivative comprises the sequence Arg-Gly-Asp-Ala-Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:1), wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val.
25. The method of claim 22 wherein the thrombin peptide derivative comprises the sequence Ala-Gly-Tyr-Lys-Pro-Asp-Glu-Gly-Lys-Arg-Gly-Asp-Ala-Cys-X 1 -Gly-Asp-Ser-Gly-Gly-Pro- 2 -Val (SEQ ID NO:2), an N-terminal truncated fragment thereof comprising at least fourteen amino acid residues, wherein X 1 is Glu or Gln and X 2 is Phe, Met, Leu, His or Val.
26. The method of claim 22 wherein the thrombin peptide derivative is H-Ala-Gly-Tyr-Lys-Pro-Asp-Glu-Gly-Lys-Arg-Gly-Asp-Ala-Cys-Glu-Gly-Asp-Ser-Gly-Gly-Pro-Phe-Val-NH 2 (SEQ ID NO3).
27. A method comprising:
contacting a medulloblastoma cancer cell with an effective amount of a thrombin peptide derivative, wherein the thrombin peptide derivative comprises the polypeptide Arg-Gly-Asp-Ala-Xaa-X 1 -Gly-Asp-Ser-Gly-Gly-Pro-X 2 -Val (SEQ ID NO:4), wherein Xaa is alanine, glycine, serine or an S-protected cysteine; X 1 is Glu or Gln; and X 2 is Phe, Met, Leu, His or Val; and
exposing the medulloblastoma cancer cell to a therapeutic radiation,
wherein the medulloblastoma cancer cell is contacted with the thrombin peptide derivative before the radiation,
wherein the thrombin peptide derivative is administered between 1 hour and 60 hours before the exposing;
and wherein the viability of the medulloblastoma cancer cell is decreased compared to the viability of the medulloblastoma cancer before the contacting and exposing.
28. The method of claim 22 wherein the thrombin derivative comprises a C-terminal amide, an acylated N-terminus, or a combination thereof, wherein said C-terminal amide is represented by —C(O)NR a R b , wherein R a and R b are independently hydrogen, an aliphatic group comprising up to 10 carbon atoms, or R a and R b , taken together with the nitrogen to which they are bonded, form a C 3 -C 10 non-aromatic heterocyclic group, and wherein said N-terminal acyl group is represented by R c C(O)—, where R c is hydrogen, an aliphatic group comprising up to 10 carbon atoms or a phenyl group optionally substituted with one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, nitro and cyano.
29. The method of claim 10 wherein the cells of the medulloblastoma having decreased viability comprise cancer stem cells.
30. The method of claim 10 wherein the administration is systemic.
31. The method of claim 30 wherein the systemic administration is intravenous.
32. The method of claim 10 wherein the subject is a child or young adult.
33. The method of claim 10 wherein the medulloblastoma is a relapse following an initial treatment.
34. The method of claim 10 wherein the thrombin derivative comprises a C-terminal amide, an acylated N-terminus, or a combination thereof, wherein said C-terminal amide is represented by —C(O)NR a R b , wherein R a and R b are independently hydrogen, an aliphatic group comprising up to 10 carbon atoms, or R a and R b , taken together with the nitrogen to which they are bonded, form a C 3 -C 10 non-aromatic heterocyclic group, and wherein said N-terminal acyl group is represented by R c C(O)—, where R c is hydrogen, an aliphatic group comprising up to 10 carbon atoms or a phenyl group optionally substituted with one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, nitro and cyano.
35. The method of claim 20 wherein the administration is systemic.
36. The method of claim 35 wherein the systemic administration is intravenous.
37. The method of claim 20 wherein the subject is a child or young adult.
38. The method of claim 20 wherein the medulloblastoma is a relapse following an initial treatment.
39. The method of claim 20 wherein the thrombin derivative comprises a C-terminal amide, an acylated N-terminus, or a combination thereof, wherein said C-terminal amide is represented by —C(O)NR a R b , wherein R a and R b are independently hydrogen, an aliphatic group comprising up to 10 carbon atoms, or R a and R b , taken together with the nitrogen to which they are bonded, form a C 3 -C 10 non-aromatic heterocyclic group, and wherein said N-terminal acyl group is represented by R c C(O)—, where R c is hydrogen, an aliphatic group comprising up to 10 carbon atoms or a phenyl group optionally substituted with one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, nitro and cyano.
40. The method of claim 27 wherein the medulloblastoma cancer cell is ex vivo.
41. The method of claim 27 wherein the thrombin derivative comprises a C-terminal amide, an acylated N-terminus, or a combination thereof, wherein said C-terminal amide is represented by —C(O)NR a R b , wherein R a and R b are independently hydrogen, an aliphatic group comprising up to 10 carbon atoms, or R a and R b , taken together with the nitrogen to which they are bonded, form a C 3 -C 10 non-aromatic heterocyclic group, and wherein said N-terminal acyl group is represented by R c C(O)—, where R c is hydrogen, an aliphatic group comprising up to 10 carbon atoms or a phenyl group optionally substituted with one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, nitro and cyano.