Compositions and methods for the prevention of cancer in high risk patients
This relates to the prevention of cancer initiation. More specifically, the invention provides compositions and methods useful for altering the genetic signature in breast tissue, said alteration being correlated with a reduced risk for the development of breast cancer.
1. A method of inhibiting the initiation of breast cancer in a subject, said method comprising providing the subject with repeated administrations of an oligopeptide selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 4, variants thereof, and acceptable salts thereof,
wherein said variant has at least 90% identity with SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 4, and
wherein each repeated administration comprises a dose of at least 0.250 mg peptide/kg bodyweight of the subject.
2. The method of claim 1 , wherein said oligopeptide administration induces genomic changes in breast tissue, said genomic changes being associated with a reduced risk for breast cancer.
3. The method according to claim 1 , wherein the repeated administrations comprises three administrations per week for three months.
4. The method of claim 1 , wherein said administration is selected from the group consisting of oral administration, transdermal administration, administration via a controlled release pump, parenteral or systemic administration and sublingual administration.
5. The method of claim 1 , wherein said oligopeptide is SEQ ID NO: 1.
6. The method of claim 1 , wherein said oligopeptide is SEQ ID NO: 2.
7. The method of claim 1 , wherein said subject has a condition selected from the group consisting of the presence of mutations in the subject associated with cancer, exposure to radiation or carcinogens and previous diagnosis of cancer.
8. The method of claim 7 , wherein said mutation is a BRCA1 or BRAC2 mutation.
9. A composition comprising a peptide having at least 90% identity with SEQ ID NO: 1 and a pharmaceutically acceptable carrier.
10. The composition of claim 9 , wherein said peptide is disposed within a liposome.
11. The composition of claim 9 , wherein said composition is within a transdermal patch.
12. The composition of claim 9 , wherein said composition is a liquid.
13. The composition of claim 9 , wherein said peptide has at least 95% identity with SEQ ID NO: 1.
14. The composition of claim 9 , wherein said peptide is SEQ ID NO: 1.
15. The method of claim 1 , wherein said variant has at least 95% identity with SEQ ID NO: 1.
16. The method of claim 1 , wherein said oligopeptide is selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 4.