US2010130589A1PendingUtilityA1

MODULATION OF eIF4E EXPRESSION

68
Assignee: FREIER SUSAN MPriority: Sep 18, 2003Filed: Aug 31, 2009Published: May 27, 2010
Est. expirySep 18, 2023(expired)· nominal 20-yr term from priority
A61P 35/00C12N 2310/32A61K 38/00C12N 15/113C12N 2310/315C12N 2310/322C12N 2310/53C12N 2310/321C12N 2310/346C07H 21/00C12N 2310/3341C12N 2310/3181C12N 2310/3231C12N 2310/13C12N 2310/341A61P 9/00A61K 31/713
68
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Claims

Abstract

Oligomeric compounds, compositions and methods are provided for modulating the expression of eIF4E. The antisense compounds may be single- or double-stranded and are targeted to nucleic acid encoding eIF4E. Methods of using these compounds for modulation of eIF4E expression and for diagnosis and treatment of diseases and conditions associated with expression of eIF4E are provided.

Claims

exact text as granted — not AI-modified
1 - 54 . (canceled) 
     
     
         55 . A modified antisense oligonucleotide, comprising the nucleotide sequence shown in SEQ ID NO:97, having at least one chemically modified internucleoside linkage, sugar moiety, or nucleobase, or a pharmaceutically acceptable salt thereof. 
     
     
         56 . The modified antisense oligonucleotide or pharmaceutically acceptable salt thereof of  claim 55 , which consists of 20 to 30 nucleotides. 
     
     
         57 . The modified antisense oligonucleotide or pharmaceutically acceptable salt thereof of  claim 55 , having at least one 2′-O-(2-methoxyethyl) sugar moiety. 
     
     
         58 . The modified antisense oligonucleotide or pharmaceutically acceptable salt thereof of  claim 55 , having at least one phosphorothioate internucleoside linkage. 
     
     
         59 . The modified antisense oligonucleotide or pharmaceutically acceptable salt thereof of  claim 55 , wherein at least one cytosine is a 5-methylcytosine. 
     
     
         60 . The modified antisense oligonucleotide or pharmaceutically acceptable salt thereof of  claim 55 , wherein every internucleoside linkage is a phosphorothioate linkage, nucleotides 1-5 and 16-20 reading from the 5′ end to the 3′ end of SEQ ID NO:97 each comprise a 2′-O-(2-methoxyethyl) sugar, nucleotides 6-15 are 2′-deoxynucleotides, and every cytosine residue is a 5-methylcytosine. 
     
     
         61 . The modified antisense oligonucleotide or pharmaceutically acceptable salt thereof of  claim 55 , which is in the form of a sodium salt. 
     
     
         62 . A modified antisense oligonucleotide, consisting of the nucleotide sequence shown in SEQ ID NO:97, wherein every internucleoside linkage is a phosphorothioate linkage, nucleotides 1-5 and 16-20 reading from the 5′ end to the 3′ end each comprise a 2′-O-(2-methoxyethyl) sugar, nucleotides 6-15 are 2′-deoxynucleotides, and every cytosine residue is a 5-methylcytosine, which modified antisense oligonucleotide is in the form of a sodium salt. 
     
     
         63 . A pharmaceutical or veterinary composition, comprising said sodium salt of said modified antisense oligonucleotide of  claim 62 , and a pharmaceutically or physiologically acceptable carrier, diluent, or excipient. 
     
     
         64 . A method of treating a condition or disease associated with eIF4E expression or overexpression in a mammal in need thereof, comprising administering to said mammal an effective amount of said sodium salt of said modified antisense oligonucleotide of  claim 62 . 
     
     
         65 . The method of  claim 64 , wherein said condition or disease associated with eIF4E expression or overexpression is a hyperproliferative condition or disease. 
     
     
         66 . The method of  claim 65 , wherein said hyperproliferative condition or disease is a susceptible cancer, tumor, or condition characterized by aberrant angiogenesis. 
     
     
         67 . The method of  claim 65 , wherein said hyperproliferative condition or disease associated with eIF4E expression or overexpression is selected from the group consisting of breast cancer, head and neck cancer, colorectal cancer, prostate cancer, lung cancer, bladder cancer, ovarian cancer, renal cancer, and glioblastoma. 
     
     
         68 . The method of  claim 64 , wherein said mammal is a human. 
     
     
         69 . A modified antisense oligonucleotide, consisting of the nucleotide sequence shown in SEQ ID NO:97, having at least one chemically modified internucleoside linkage, sugar moiety, or nucleobase, which modified antisense oligonucleotide is in the form of a sodium salt. 
     
     
         70 . The modified antisense oligonucleotide of  claim 69 , wherein every internucleoside linkage is a phosphorothioate linkage, nucleotides 1-5 and 16-20 reading from the 5′ end to the 3′ end each comprise a 2′-O-(2-methoxyethyl) sugar, nucleotides 6-15 are 2′-deoxynucleotides, and at least one cytosine is a 5-methylcytosine, which modified antisense oligonucleotide is in the form of a sodium salt.

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