Therapeutic and diagnostic molecules
Abstract
The present invention relates to methods for modulating angiogenesis, comprising administering to a subject, or cells or tissue derived therefrom: (i) one or more miRNA, or precursors or variants thereof, wherein at least one of said miRNA comprises a seed region comprising the sequence UCACAGU (SEQ ID NO:37) to inhibit angiogenesis; or (ii) one or more antagonists of a miRNA, wherein said miRNA comprises a seed region comprising the sequence UCACAGU (SEQ ID NO:37) to promote or induce angiogenesis. Also provided are methods of diagnosis of conditions associated with abnormal angiogenesis, or determining predisposition thereto. Suitable pharmaceutical compositions are also provided.
Claims
exact text as granted — not AI-modified1 . A method for increasing the expression of VE-cadherin protein in a cell or tissue of a subject, the method comprising administering to the subject, or a cell or tissue derived therefrom, an effective amount of one or more antagonists of a miRNA comprising a seed region comprising the sequence UCACAGU (SEQ ID No. 37).
2 . The method of claim 1 wherein the miRNA comprising the seed region sequence UCACAGU is miR_27a.
3 . The method of claim 2 wherein the miR_27a is hsa_miR_27a and comprises the nucleotide sequence set forth in SEQ ID NO:1.
4 . The method of claim 1 wherein the antagonist is an antisense oligonucleotide specific for the miRNA.
5 . The method of claim 4 wherein the antisense oligonucleotide comprises a nucleotide sequence as set forth in SEQ ID NO:19.
6 . The method of claim 4 wherein the oligonucleotide sequence comprises one or more modifications such as non-naturally occurring nucleotide analogues, non-phosphate linkages between nucleotides, and/or conjugated moieties.
7 . A method for decreasing endothelial cell permeability in a cell or tissue of a subject, the method comprising administering to the subject, or a cell or tissue derived therefrom, an effective amount of one or more antagonists of a miRNA comprising a seed region comprising the sequence UCACAGU (SEQ ID No. 37).
8 . The method of claim 7 wherein the miRNA comprising the seed region sequence UCACAGU is miR_27a.
9 . The method of claim 8 wherein the miR_27a is hsa_miR_27a and comprises the nucleotide sequence set forth in SEQ ID NO:1.
10 . The method of claim 7 wherein the antagonist is an antisense oligonucleotide specific for the miRNA.
11 . The method of claim 10 wherein the antisense oligonucleotide comprises a nucleotide sequence as set forth in SEQ ID NO:19.
12 . The method of claim 10 wherein the oligonucleotide sequence comprises one or more modifications such as non-naturally occurring nucleotide analogues, non-phosphate linkages between nucleotides, and/or conjugated moieties.
13 . A method for decreasing the expression of VE-cadherin protein in a cell or tissue of a subject, the method comprising administering to the subject, or a cell or tissue derived therefrom, an effective amount of a miRNA comprising a seed region comprising the sequence UCACAGU (SEQ ID No. 37).
14 . The method of claim 13 wherein the miRNA comprising the seed region sequence UCACAGU is miR_27a.
15 . The method of claim 14 wherein the miR_27a is hsa_miR_27a and comprises the nucleotide sequence set forth in SEQ ID NO:1.
16 . A method for increasing endothelial cell permeability in a cell or tissue of a subject, the method comprising administering to the subject, or a cell or tissue derived therefrom, an effective amount of a miRNA comprising a seed region comprising the sequence UCACAGU (SEQ ID No. 37).
17 . The method of claim 16 wherein the miRNA comprising the seed region sequence UCACAGU is miR_27a.
18 . The method of claim 17 wherein the miR_27a is hsa_miR_27a and comprises the nucleotide sequence set forth in SEQ ID NO:1.Join the waitlist — get patent alerts
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