US2005049211A1PendingUtilityA1
Antisense modulation of insulin-like growth factor binding protein 5 expression
Priority: Oct 9, 2001Filed: Oct 7, 2002Published: Mar 3, 2005
Est. expiryOct 9, 2021(expired)· nominal 20-yr term from priority
Inventors:Susan M. Freier
C12N 2310/315A61K 38/28C12N 2310/3341C12N 2310/11C12N 15/09C12N 2310/341A61K 38/00C12N 15/113C12N 2310/346C12N 2310/321Y02P20/582
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Claims
Abstract
Antisense compounds, compositions and methods are provided for modulating the expression of insulin-like growth factor binding protein 5. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding insulin-like growth factor binding protein 5. Methods of using these compounds for modulation of insulin-like growth factor binding protein 5 expression and for treatment of diseases associated with expression of insulin-like growth factor binding protein 5 are provided.
Claims
exact text as granted — not AI-modified1 . A compound 8 to 50 nucleobases in length targeted to the start codon, the coding region, the 3′ untranslated region, an intron or an intron/exon junction of a nucleic acid molecule encoding insulin-like growth factor binding protein 5, wherein said compound specifically hybridizes with said nucleic acid molecule encoding insulin-like growth factor binding protein 5 and inhibits the expression of insulin-like growth factor binding protein 5.
2 . The compound of claim 1 which is an antisense oligonucleotide.
3 . The compound of claim 2 wherein the antisense oligonucleotide has a sequence comprising SEQ ID NO: 13, 14, 15, 16, 17, 18, 19, 21, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 38, 39, 40, 41, 42 or 43.
4 . The compound of claim 2 wherein the antisense oligonucleotide comprises at least one modified internucleoside linkage.
5 . The compound of claim 4 wherein the modified internucleoside linkage is a phosphorothioate linkage.
6 . The compound of claim 2 wherein the antisense oligonucleotide comprises at least one modified sugar moiety.
7 . The compound of claim 6 wherein the modified sugar moiety is a 2′-O-methoxyethyl sugar moiety.
8 . The compound of claim 2 wherein the antisense oligonucleotide comprises at least one modified nucleobase.
9 . The compound of claim 8 wherein the modified nucleobase is a 5-methylcytosine.
10 . The compound of claim 2 wherein the antisense oligonucleotide is a chimeric oligonucleotide.
11 . A compound 8 to 50 nucleobases in length which specifically hybridizes with at least an 8-nucleobase portion of an active site on a nucleic acid molecule encoding insulin-like growth factor binding protein 5.
12 . A composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier or diluent.
13 . The composition of claim 12 further comprising a colloidal dispersion system.
14 . The composition of claim 12 wherein the compound is an antisense oligonucleotide.
15 . A method of inhibiting the expression of insulin-like growth factor binding protein 5 in cells or tissues comprising contacting said cells or tissues with the compound of claim 1 so that expression of insulin-like growth factor binding protein 5 is inhibited.
16 . A method of treating an animal having a disease or condition associated with insulin-like growth factor binding protein 5 comprising administering to said animal a therapeutically or prophylactically effective amount of the compound of claim 1 so that expression of insulin-like growth factor binding protein 5 is inhibited.
17 . The method of claim 16 wherein the disease or condition is a hyperproliferative disorder.
18 . The method of claim 17 wherein the hyperproliferative disorder is cancer.
19 . The method of claim 18 wherein the cancer is of the breast, prostate, pancreas, or neuroendocrine system.
20 . The method of claim 16 wherein the disease or condition is an inflammatory, developmental or metabolic disorder.Join the waitlist — get patent alerts
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