发明名称 |
SDF-1 binding nucleic acids and the use thereof in cancer treatment |
摘要 |
The present invention is related to a nucleic acid molecule capable of binding to SDF-1, preferably capable of inhibiting SDF-1, whereby the nucleic acid molecule is for use in a method for the treatment and/or prevention of a disease or disorder, for use in a method for the treatment of a subject suffering from a disease or disorder or being at risk of developing a disease or disorder as an adjunct therapy, or for use as a medicament for the treatment and/or prevention of a disease or disorder, whereby the disease or disorder is cancer. |
申请公布号 |
US9387221(B2) |
申请公布日期 |
2016.07.12 |
申请号 |
US201514947173 |
申请日期 |
2015.11.20 |
申请人 |
NOXXON Pharma AG |
发明人 |
Purschke Werner;Jarosch Florian;Eulberg Dirk;Klussmann Sven;Buchner Klaus;Maasch Christian;Dinse Nicole;Zboralski Dirk |
分类号 |
C12N15/11;A61K48/00;C07H21/02;C12N15/115;A61K31/713;A61K45/06 |
主分类号 |
C12N15/11 |
代理机构 |
MDIP LLC |
代理人 |
MDIP LLC |
主权项 |
1. A method for the treatment of a subject suffering from cancer comprising:
a) administering to the subject a cancer-treating amount of an L-nucleic acid molecule, or a an L-nucleic acid homolog thereof, wherein said L-nucleic acid molecule comprises SEQ ID NO:22, and said L-nucleic acid homolog comprises SEQ ID NO: 52 and a 5′ terminal stretch of nucleotides and a 3′ terminal stretch of nucleotides, wherein said 5′ stretch and said 3′ stretch can hybridize to each other, wherein
1) when said homolog is shorter than SEQ ID NO: 22, said homolog comprises homology of at least 85% to SEQ ID NO: 22 over the entire length of said homolog, and2) when said homolog is equal in length to or longer than SEQ ID NO: 22, said homolog comprises homology of at least 85% to SEQ ID NO: 22 over the entire length of SEQ ID NO: 22, and wherein said L-nucleic acid molecule and said L-nucleic acid homolog bind SDF-1 and inhibit interaction of (a) SDF-1 and CXCR4 and (b) SDF-1 and CXCR7. |
地址 |
Berlin DE |