IP Library Granted Patent US 10,450,572
Granted Patent B2
US 10,450,572 · App. 15/675,072 · Granted Oct 22, 2019

Androgen receptor variant inhibitors and methods of using

Inventors: Jamie Lynn Van Etten (Minneapolis, MN); Scott M. Dehm (Rochester, MN)
Assignee: Regents of the University of Minnesota
C12N15/1138A61K31/713A61K45/06A61P35/00C12N2310/11C12N2310/314C12N2310/3233C12N2310/3513C12N2320/31C12N2320/33
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Quick Facts
Patent No.
US 10,450,572
App. No.
15/675,072
Granted
Oct 22, 2019
Kind
B2
Abstract

This document relates to materials and methods for treating cancer (e.g., prostate cancer). For example, methods for using one or more androgen receptor variant (AR-V) inhibitors (e.g., morpholinos) to treat a mammal having prostate cancer (e.g., castration-resistant prostate cancer) are provided.

Claims (30)

1. An androgen receptor variant (AR-V) inhibitor oligonucleotide, wherein said AR-V inhibitor oligonucleotide comprises:

an antisense sequence about 22 nucleotides to about 200 nucleotides in length which is complementary to a target sequence in cryptic exon 3 of an AR transcript, wherein said antisense sequence comprises at least one modified nucleotide, wherein said antisense sequence has at least 90 percent sequence identity to SEQ ID NO:2, and wherein said antisense sequence comprises SEQ ID NO:1; and

wherein said AR-V inhibitor oligonucleotide binds to the AR transcript and inhibits expression of one or more AR-Vs.

2. The AR-V inhibitor oligonucleotide of claim 1 , wherein said antisense sequence is about 22 to about 30 nucleotides in length.

3. The AR-V inhibitor oligonucleotide of claim 1 , wherein said antisense sequence comprises SEQ ID NO:2.

4. The AR-V inhibitor oligonucleotide of claim 1 , wherein said target sequence comprises a polyadenylation site.

5. The AR-V inhibitor oligonucleotide of claim 1 , wherein said target sequence comprises SEQ ID NO:3.

6. The AR-V inhibitor oligonucleotide of claim 5 , wherein said target sequence comprises SEQ ID NO:4.

7. The AR-V inhibitor oligonucleotide of claim 1 , wherein said one or more AR-Vs are selected from the group consisting of AR-V2, AR-V5, AR-V7, and/or AR-V9.

8. The AR-V inhibitor oligonucleotide of claim 7 , wherein said AR-V inhibitor oligonucleotide inhibits expression of AR-V7.

9. The AR-V inhibitor oligonucleotide of claim 1 , wherein said AR-V inhibitor oligonucleotide is conjugated to a cell-penetrating peptide.

10. The AR-V inhibitor oligonucleotide of claim 9 , wherein said cell-penetrating peptide comprises an 8 guanidine head group.

11. The AR-V inhibitor oligonucleotide of claim 1 , wherein said at least one modified nucleotide comprises a morpholine ring.

12. The AR-V inhibitor oligonucleotide of claim 1 , wherein said at least one modified nucleotide comprises a phosphorodiamidate linkage.

13. The AR-V inhibitor oligonucleotide of claim 1 , wherein said AR-V inhibitor oligonucleotide is a morpholino.

14. A method for treating castration-resistant prostate cancer (CRPC) in a mammal, the method comprising:

identifying said mammal as having a CRPC expressing one or more androgen receptor variants (AR-Vs); and

administering to said mammal an AR-V inhibitor oligonucleotide, wherein said AR-V inhibitor oligonucleotide comprises an antisense sequence about 22 nucleotides to about 200 nucleotides in length which is complementary to a target sequence in cryptic exon 3 of an AR transcript, wherein said antisense sequence comprises at least one modified nucleotide, wherein said antisense sequence has at least 90 percent sequence identity to SEQ ID NO:2, and wherein said antisense sequence comprises SEQ ID NO:1;

wherein said AR-V inhibitor oligonucleotide binds to the AR transcript and inhibits expression of one or more AR-Vs.

15. The method of claim 14 , wherein said mammal is a human.

16. The method of claim 14 , wherein said one or more AR-Vs are selected from the group consisting of AR-V2, AR-V5, AR-V7, and/or AR-V9.

17. The method of claim 16 , wherein said AR-V inhibitor oligonucleotide inhibits expression of AR-V7.

18. The method of claim 14 , wherein said AR-V inhibitor oligonucleotide restores androgen responsiveness to a CRPC.

19. The method of claim 14 , wherein said antisense sequence comprises SEQ ID NO:2.

20. The method of claim 14 , wherein said target comprises a polyadenylation site.

21. The method of claim 14 , wherein said target sequence comprises SEQ ID NO:3.

22. The method of claim 21 , wherein said target sequence comprises SEQ ID NO:4.

23. The method of claim 14 , wherein said AR-V inhibitor oligonucleotide is a morpholino.

24. The method of claim 23 , wherein said additional cancer treatment comprises androgen deprivation therapy.

25. The method of claim 24 , wherein said androgen deprivation therapy comprises administering an antiandrogen.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2019
From: VAN ETTEN, JAMIE LYNN
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 050259/0705 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2018
From: DEHM, SCOTT M.
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 047511/0518 →
CONFIRMATORY LICENSE Recorded Nov 29, 2017
From: UNIVERSITY OF MINNESOTA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044531/0180 →
Continuity (2)
Provisional Application 62374482 · Aug 12, 2016
Related Publication 20180119153A1 · May 3, 2018