US2019183946A1PendingUtilityA1

Oncolytic adenoviruses for cancer treatment

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Assignee: DNATRIX INCPriority: Feb 1, 2006Filed: Jul 5, 2018Published: Jun 20, 2019
Est. expiryFeb 1, 2026(expired)· nominal 20-yr term from priority
C12N 2710/10343C12N 2710/10032C12N 2710/10321C12N 2710/10043C12N 2710/10332C12N 15/86C12N 2820/007A61K 35/761A61P 35/00C12N 2710/10021C12N 7/00C12N 15/8613
62
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Claims

Abstract

The invention relates to an oncolytic adenovirus for the treatment of cancer, containing a human DNA sequence isolating a promoter conferring selective expression on an adenoviral gene. Said adenovirus can also contain a sequence that optimizes the protein translation of an adenoviral gene regulated by a promoter conferring tumor selectivity. The invention is suitable for use in the treatment of cancer.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . An oncolytic adenovirus comprising: an adenoviral gene operably linked to a tumor selective promoter that confers tumor selective expression of the adenoviral gene; and upstream of the promoter, a myotonic dystrophy insulator that comprises a CTCF binding site. 
     
     
         2 . The oncolytic adenovirus according to  claim 1 , wherein a Kozak sequence is operably linked at the 5′ end of the adenoviral gene to optimize protein translation. 
     
     
         3 . The oncolytic adenovirus according to  claim 1 , wherein the adenovirus capsid is modified to increase infectivity or to direct the adenovirus to a receptor present on a tumor cell. 
     
     
         4 . The oncolytic adenovirus according to  claim 1 , wherein a Kozak sequence is operably linked at the 5′ end of the adenoviral gene to optimize protein translation; and the capsid is modified to increase infectivity or to direct the adenovirus to a receptor present on a tumor cell. 
     
     
         5 . The oncolytic adenovirus according to  claim 1 , wherein the adenovirus further comprises one or more other genes encoding proteins chosen from prodrug activators, tumor suppressors, and immunostimulators. 
     
     
         6 . The oncolytic adenovirus according to  claim 1 , wherein a Kozak sequence is operably lined at the 5′ end of the adenoviral gene to optimize protein translation; and the adenovirus comprises one or more other genes encoding proteins chosen from prodrug activators, tumor suppressors, and immunostimulators. 
     
     
         7 . The oncolytic adenovirus according to  claim 1 , wherein the adenovirus is a human adenovirus serotype from 1 to 50. 
     
     
         8 . The oncolytic adenovirus according to  claim 7 , wherein the adenovirus genome is from a human adenovirus serotype 5. 
     
     
         9 . The oncolytic adenovirus according to  claim 1 , wherein the promoter is the promoter of human gene E2F1. 
     
     
         10 . The oncolytic adenovirus according to  claim 9 , wherein the E2F1 promoter is modified by the insertion of additional binding sites to E2F. 
     
     
         11 . A pharmaceutical composition comprising an effective amount of the oncolytic adenovirus according to  claim 1 , and one or more components chosen from carriers and pharmaceutically acceptable excipients. 
     
     
         12 . The oncolytic adenovirus according to  claim 1 , wherein the sequence of the insulator comprises position 368 to 1096 of the nucleotide sequence of SEQ ID No:1.

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