Rna antagonist compounds for the modulation of her3

Abstract

The invention relates to oligomer compounds (oligomers), which target HER3 mRNA in a cell, leading to reduced expression of HER3 and/or HER2 and/or EGFR. Reduction of HER3 and/or HER2 and/or EGFR expression is beneficial for a range of medical disorders, such hyperproliferative disorders (e.g., cancer). The invention provides therapeutic compositions comprising oligomers and methods for modulating the expression of HER3 and/or HER2 and/or EGFR using said oligomers, including methods of treatment.

1 - 30 . (canceled) 
     
     
         31 . An oligomer selected from the group consisting of: 
       
         
           
                 
                 
               
                     
                   (SEQ ID NO: 169) 
                 
                     
                   5′-G s   Me C s T s c s c s a s g s a s c s a s t s c s a s   Me C s T s   Me C-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 172) 
                 
                     
                   5′-A s G s A s c s a s t s c s a s c s t s c s t s g s G s T s G-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 173) 
                 
                     
                   5′-A s T s A s g s c s t s c s c s a s g s a s c s a s T s   Me C s A-3′, 
                 
                     
                   and 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 174) 
                 
                     
                   5′-T s   Me C s A s c s a s c s c s a s t s a s g s c s t s   Me C s   Me C s A-3′, 
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
       wherein uppercase letters denote beta-D-oxy-LNA monomers and lowercase letters denote DNA monomers, the subscript “s” denotes a phosphorothioate linkage, and  Me C denotes a beta-D-oxy-LNA monomer containing a 5-methylcytosine base. 
     
     
         32 . The oligomer according to claim  1 , which inhibits the expression of a human HER3 gene or mRNA in a cell that expresses HER3. 
     
     
         33 . A pharmaceutical composition comprising the oligomer according to claim  1 , and a pharmaceutically acceptable diluent, carrier, salt or adjuvant. 
     
     
         34 . A conjugate comprising an oligomer according to claim  1  covalently attached to at least one moiety that is not a nucleic acid or a monomer. 
     
     
         35 . A pharmaceutical composition comprising the conjugate according to  claim 34 , and a pharmaceutically acceptable diluent, carrier, salt or adjuvant. 
     
     
         36 . A method of inhibiting the expression of HER3 in a cell, comprising contacting said cell with an oligomer selected from the group consisting of: 
       
         
           
                 
                 
               
                     
                   (SEQ ID NO: 169) 
                 
                     
                   5′-G s   Me C s T s c s c s a s g s a s c s a s t s c s a s   Me C s T s   Me C-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 172) 
                 
                     
                   5′-A s G s A s c s a s t s c s a s c s t s c s t s g s G s T s G-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 173) 
                 
                     
                   5′-A s T s A s g s c s t s c s c s a s g s a s c s a s T s   Me C s A-3′, 
                 
                     
                   and 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 174) 
                 
                     
                   5′-T s   Me C s A s c s a s c s c s a s t s a s g s c s t s   Me C s   Me C s A-3′, 
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
       wherein uppercase letters denote beta-D-oxy-LNA monomers and lowercase letters denote DNA monomers, the subscript “s” denotes a phosphorothioate linkage, and  Me C denotes a beta-D-oxy-LNA monomer containing a 5-methylcytosine base. 
     
     
         37 . A method of inhibiting the expression of HER3 in a cell, comprising contacting said cell with an effective amount of a conjugate according to  claim 34 . 
     
     
         38 . A method of inhibiting the expression of HER3 in a tissue of a mammal, comprising contacting said tissue with an effective amount of an oligomer selected from the group consisting of: 
       
         
           
                 
                 
               
                     
                   (SEQ ID NO: 169) 
                 
                     
                   5′-G s   Me C s T s c s c s a s g s a s c s a s t s c s a s   Me C s T s   Me C-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 172) 
                 
                     
                   5′-A s G s A s c s a s t s c s a s c s t s c s t s g s G s T s G-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 173) 
                 
                     
                   5′-A s T s A s g s c s t s c s c s a s g s a s c s a s T s   Me C s A-3′, 
                 
                     
                   and 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 174) 
                 
                     
                   5′-T s   Me C s A s c s a s c s c s a s t s a s g s c s t s   Me C s   Me C s A-3′, 
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
       wherein uppercase letters denote beta-D-oxy-LNA monomers and lowercase letters denote DNA monomers, the subscript “s” denotes a phosphorothioate linkage, and  Me C denotes a beta-D-oxy-LNA monomer containing a 5-methylcytosine base. 
     
     
         39 . A method of inhibiting the expression of HER3 in a tissue of a mammal comprising contacting said tissue with an effective amount of a conjugate according to  claim 34 . 
     
     
         40 . A method of treating cancer in a mammal, comprising administering to said mammal an effective amount of an oligomer selected from the group consisting of: 
       
         
           
                 
                 
               
                     
                   (SEQ ID NO: 169) 
                 
                     
                   5′-G s   Me C s T s c s c s a s g s a s c s a s t s c s a s   Me C s T s   Me C-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 172) 
                 
                     
                   5′-A s G s A s c s a s t s c s a s c s t s c s t s g s G s T s G-3′, 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 173) 
                 
                     
                   5′-A s T s A s g s c s t s c s c s a s g s a s c s a s T s   Me C s A-3′, 
                 
                     
                   and 
                 
                     
                     
                 
                     
                   (SEQ ID NO: 174) 
                 
                     
                   5′-T s   Me C s A s c s a s c s c s a s t s a s g s c s t s   Me C s   Me C s A-3′, 
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
       wherein uppercase letters denote beta-D-oxy-LNA monomers and lowercase letters denote DNA monomers, the subscript “s” denotes a phosphorothioate linkage, and  Me C denotes a beta-D-oxyLNA monomer containing a 5-methylcytosine base. 
     
     
         41 . The method of  claim 40 , wherein the cancer is selected from non-Hodgkin's lymphoma, Hodgkin's lymphoma, acute leukemia such as acute lymphocytic leukemia, acute myelocytic leukemia, chronic myeloid leukemia, chronic lymphocytic leukemia, multiple myeloma, colon carcinoma, rectal carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, cervical cancer, testicular cancer, lung carcinoma, bladder carcinoma, melanoma, head and neck cancer, brain cancer, cancers of unknown primary site, neoplasms, cancers of the peripheral nervous system, cancers of the central nervous system, fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumour, leiomyosarcoma, rhabdomyosarcoma, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogcnic carcinoma, seminoma, embryonal carcinoma, Wilms' tumour, small cell lung carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pincaloma, hemamio blastoma, acoustic neuroma, oligodendroglioma, meningioma, neuroblastoma, and retinoblastoma