IP Library Granted Patent US 7,368,436
Granted Patent B2
US 7,368,436 · App. 09/944,326 · Granted May 6, 2008

TRPM-2 antisense therapy

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Quick Facts
Patent No.
US 7,368,436
App. No.
09/944,326
Granted
May 6, 2008
Kind
B2
Abstract

It has been determined that antisense therapy which reduces the expression of TRPM- 2 provides therapeutic benefits in the treatment of cancer, particularly prostate and renal cell cancers. Addition of antisense TRPM- 2 ODN to prostatic tumor cells in vivo is effective for delaying the onset of androgen independence, thus prostate cancer can be treated by initiating androgen-withdrawal to induce apoptotic cell death of prostatic tumor cells in an individual, and administering a composition effective to inhibit expression of TRPM- 2 by the tumor cells. Combined use of antisense TRPM- 2 and taxanes synergistically enhances cytotoxic chemosensitivity of androgen-independent prostate cancer and in human Renal cell cancer. Radiation sensitivity is also enhanced when cells expressing TRPM- 2 are treated with antisense TRPM- 2 ODN. Thus, the antisense TRPM- 2 ODNs can be used to enhance hormone sensitivity, chemosensitivity and radiation sensitivity of a variety of cancer types in which expression of TRPM- 2 has been observed.

Claims (8)

1. A pharmaceutical composition, comprising an antisense oligonucleotide which inhibits expression of TRPM-2 by tumor cells, and a pharmaceutically acceptable carrier suitable for human administration for providing the oligonucleotide to a mammalian subject to reduce expression of TRPM-2 wherein the antisense oligonucleotide comprises the sequence given by SEQ ID No. 4 and wherein the composition further comprises a second antisense oligodeoxynucleotide which inhibits expression of an anti-apoptotic protein other than TRPM-2.

2. The composition of claim 1 , wherein the second antisense oligodeoxynucleotide is antisense Bcl-2 oligodeoxynucleotide.

3. The composition of claim 2 , wherein the antisense oligonucleotide having the sequence given by SEQ ID No. 4 is modified to increase the stability of the ODN in vivo.

4. The pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable carrier is a lipid carrier.

5. A pharmaceutical composition, comprising an antisense oligonucleotide which inhibits expression of TRPM-2 by tumor cells, and a pharmaceutically acceptable carrier suitable for human administration for providing the oligonucleotide to a mammalian subject to reduce expression of TRPM-2 wherein the antisense oligonucleotide comprises the sequence given by SEO ID No. 4, wherein the composition further comprises an additional antisense oligonucleotide that binds specifically to a sequence other than TRPM-2 mRNA.

6. The pharmaceutical composition according to claim 5 , wherein the additional antisense oligonucleotide binds specifically to a sequence selected from among Bcl-2, Bcl-1x and c-myc.

7. The pharmaceutical composition according to claim 6 , wherein the additional oligonucleotide consists of the sequence set forth in the Seq. ID No. 13.

8. The pharmaceutical composition of claim 1 , where the oligonucleotide consists of the sequence given by SEQ ID No. 4.

Assignments (3)
CHANGE OF NAME Recorded Jul 26, 2017
From: ISIS PHARMACEUTICALS, INC.
To: IONIS PHARMACEUTICALS, INC.
Reel/Frame 043341/0891 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2003
From: GLEAVE, MARTIN; RENNIE, PAUL S.; MIYAKE, HIDEAKI; NELSON, COLLEEN
To: BRITISH COLUMBIA, THE UNIVERSITY OF
Reel/Frame 014480/0492 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2002
From: GLEAVE, MARTIN; RENNIE, PAUL S.; MIYAKE, HIDEAKI; NELSON, COLLEEN
To: BRITISH COLUMBIA, UNIVERSITY OF
Reel/Frame 012521/0568 →