US2007117748A1PendingUtilityA1
Novel apoptosis-modulating proteins, dna encoding the proteins and methods of use thereof
Est. expiryNov 30, 2013(expired)· nominal 20-yr term from priority
A61P 7/06A61P 43/00A61P 9/10A61P 37/02A61P 9/00A61P 37/06A61P 3/10A61P 3/04A61P 25/00A61P 27/02A61P 31/12A61P 35/00A61P 31/04A01K 2217/05C07K 14/4747A61K 38/00A61P 1/12A61P 1/00A61P 13/08C12Q 2600/158A61P 17/14C12Q 1/6876C12N 15/8509A01K 2267/025A01K 2267/03A01K 2227/105
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Claims
Abstract
The present invention provides a novel family of apoptosis-modulating proteins. Nucleotide and amino acid residue sequences and methods of use thereof are also provided.
Claims
exact text as granted — not AI-modified1 - 58 . (canceled)
59 . An antisense molecule comprising an oligonucleotide of length sufficient to modulate apoptosis, wherein said antisense oligonucleotide is complementary to a polynucleotide encoding CDN-1, CDN-2, CDN-3, CDN1Δ1, CDN1Δ2, or CDN1Δ3.
60 . The antisense compound of claim 59 , which is targeted to a nucleic acid molecule encoding CDN-1 and which preferentially inhibits the expression of CDN-1.
61 . The antisense compound of claim 59 , which promotes apoptosis.
62 . The antisense compound of claim 59 , which inhibits apoptosis.
63 . A pharmaceutical composition comprising the antisense molecule of claim 59 and a pharmaceutically acceptable carrier or diluent.
64 . A method of modulating apoptosis in a cell in a mammal diagnosed as having a proliferative disease, comprising administering to said mammal an antisense oligonucleotide of claim 59 .
65 . The method of claim 64 , wherein said mammal is a human.
66 . The method of claim 64 , wherein said proliferative disease is cancer.
67 . A method to modulate apoptosis-induced cell death, comprising contacting an endogenous polynucleotide encoding SEQ ID NO:7 in a cell with an antisense polynucleotide that inhibits the expression of the polynucleotide encoding SEQ ID NO:7.
68 . The method of claim 67 , wherein the antisense polynucleotide hybridizes under highly stringent conditions to a gene encoding SEQ ID NO:7.
69 . The method of claim 67 , wherein the antisense polynucleotide is fully complementary to a polynucleotide encoding SEQ ID NO:7.
70 . The method of claim 67 , wherein the antisense polynucleotide is fully complementary to a polynucleotide encoding a fragment of SEQ ID NO:7 lacking up to about the first 70 amino acids of SEQ ID NO:7, wherein the fragment modulates apoptosis in a cell.
71 . The method of claim 67 , wherein the antisense polynucleotide is fully complementary to a polynucleotide encoding a fragment of SEQ ID NO:7 truncated after about amino acid position 112, wherein the fragment modulates apoptosis in a cell.
72 . The method of claim 67 , wherein the antisense polynucleotide is fully complementary to a polynucleotide encoding an amino acid sequence that that is greater than 97% identical to SEQ ID NO:7, wherein the amino acid sequence modulates apoptosis in a cell.
73 . The method of claim 67 , wherein apoptosis-induced cell death is increased in the cell in the presence of the polynucleotide as compared to in the absence of the polynucleotide.
74 . The method of claim 67 , wherein the cell displays uncontrolled cell growth.
75 . The method of claim 74 , wherein the cell is a cancer cell.
76 . The method of claim 74 , wherein the cell is from a B cell lymphoma.Cited by (0)
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