Claims for Patent: 5,645,995

Summary for Patent: 5,645,995

Title:	Methods for diagnosing an increased risk for breast or ovarian cancer
Abstract:	The present invention relates to methods for diagnosing an increased risk for breast or ovarian cancer by assaying for genetic markers in the human progesterone receptor gene.
Inventor(s):	Kieback; Dirk G. (Houston, TX)
Assignee:	Baylor College of Medicine (Houston, TX)
Application Number:	08/629,939
Patent Claims:	1. A method for diagnosing an increased risk for breast or ovarian cancer comprising the steps of: (A) obtaining, from a test subject, test nucleic acid comprising codon 660 within EXON 4 of the human progesterone receptor gene; and (B) assaying for the presence of a G to T point mutation in the first nucleotide of codon 660 within EXON 4 of the human progesterone receptor gene, wherein the presence of said point mutation in said test nucleic acid indicates an increased risk for breast or ovarian cancer. 2. The method of claim 1, wherein said method additionally comprises the steps of: (C) obtaining, from said test subject, test nucleic acid which comprises codon 770 within EXON 5 of the human progesterone receptor gene, and (D) assaying for the presence of a C to T point mutation in the third nucleotide of codon 770 within EXON 5 of the human progesterone receptor gene, wherein the presence of said point mutation in said test nucleic acid comprising codon 770 of exons indicates an increased risk for breast or ovarian cancer. 3. The method of claims 1 or 2, wherein said method additionally comprises the steps of: (E) obtaining, from said test subject, test nucleic acid which comprises codon 897 within INTRON G of the human progesterone receptor gene, and (F) assaying for the presence of an Alu insertion within codon 897 within INTRON G of the human progesterone receptor gene, wherein the presence of said Alu insertion in said test nucleic acid comprising codon 897 of INTRON G indicates an increased risk for breast or ovarian cancer. 4. The method of claim 1, wherein said assaying in step (B) is carried out by subjecting said test nucleic acid to BsrI restriction enzyme digestion, and assaying for the loss of a BsrI restriction site within EXON 4 of the human progesterone receptor gone, wherein the loss of said restriction site indicates the presence of said point mutation. 5. The method of claim 1, wherein said assaying in step (B) is carried out by sequencing said test nucleic acid. 6. The method of claim 1, wherein said assaying in step (B) is carried out by single-strand conformation polymorphism analysis. 7. The method of claim 1, wherein said assaying in step (B) is carried out by heteroduplex mapping. 8. The method of claim 2, wherein said assaying in step (D) is carried out by subjecting said test nucleic acid comprising codon 770 of EXON 5 to NlaIII restriction enzyme digestion, and assaying for the addition of a NlaIII restriction site within EXON 5 of the human progesterone receptor gene, wherein the addition of said restriction site indicates the presence of said point mutation. 9. The method of claim 2, wherein said assaying in step (D) is carried out by sequencing said test nucleic acid comprising codon 770 EXON 5. 10. The method of claim 2, wherein said assaying in step (D) is carried out by single-strand conformation polymorphism analysis. 11. The method of claim 2, wherein said assaying in step (D) is carried out by heteroduplex mapping. 12. The method of claim 3, wherein said assaying in step (F) is carried out by subjecting said test nucleic acid comprising codon 897 of INTRON G to TaqI restriction enzyme digestion, and assaying for the production of a 1.9 kb DNA fragment, wherein the production of said 1.9 kb DNA fragment indicates the presence of said Alu insertion. 13. The method of claim 3, wherein said assaying in step (F) is carried out by polymerase chain reaction using forward and reverse primers that border or are within INTRON G. 14. The method of claim 13, wherein said primers boarder INTRON G, and wherein said forward primer is: 15. The method of claim 13, wherein said primers are within INTRON G, and wherein said forward primer is: 16. The method of claim 3, wherein said assaying in step (F) is carried out by sequencing said test nucleic acid comprising codon 897 of INTRON G. 17. The method of claim 3, wherein said assaying in step (F) is carried out by heteroduplex mapping. 18. The method of claim 3, wherein said assaying in step (F) is carried out by florescent in situ hybridization using an oligonucleotide consisting of SEQ ID NO:10. 19. The method of claim 3, wherein said assaying in step (F) is carried out by Southern blotting using a probe comprising said Alu insertion. 20. The method of claim 1, wherein said test nucleic acid is obtained from cells within a body fluid of said subject, wherein said body fluid is selected from the group consisting of blood, ascites, pleural fluid and spinal fluid. 21. The method of claim 1, wherein said test nucleic acid is obtained from cells constituting a body tissue of said subject, wherein said body tissue is selected from the group consisting of skin, endometrial, uterine and cervical tissue. 22. The method of claim 1, wherein said test nucleic acid is genomic DNA, cDNA or mRNA. 23. The method of claim 2, wherein said test nucleic acid comprising codon 770 of EXON 5. 24. The method of claim 3, wherein said test nucleic acid used to assay for the Alu insertion in Step (F) is genomic DNA.

Details for Patent 5,645,995

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132	06/04/1986		2039-02-26
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132			2039-02-26
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	Injection	103132			2039-02-26