TRPM-2 antisense therapy using an oligonucleotide having 2'-O-(2-methoxy)ethyl modifications
AssigneeThe University of British Columbia
InventorsMartin Gleave, Paul S. Rennie, Hideaki Miyake, Colleen Nelson, Brett P. Monia
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Abstract
A compound consisting of an oligonucleotide of sequence CAGCAGCAGAGTCTTCATCAT, where the oligonucleotide has a phosphorothioate backbone throughout, the sugar moieties of nucleotides 1-4 and 18-21 bear 2′-O-methoxyethyl modifications, and the remaining nucleotides (nucleotides 5-17) are 2′-deoxynucleotides, and where the cytosines of nucleotides 1, 4 and 19 are 5-methylcytosines. The compound has increased stability in vivo and improved in vitro and in vivo antitumor activity.
Claims11
A compound consisting of an oligonucleotide of sequence CAGCAGCAGAGTCTTCATCAT;
- SEQ ID NO:
- 4, wherein the oligonucleotide has a phosphorothioate backbone throughout, the sugar moieties of nucleotides 1-4 and 18-21 bear 2′-O-methoxyethyl modifications, and the remaining nucleotides (nucleotides 5-17) are 2′-deoxynucleotides, and wherein the cytosines of nucleotides 1, 4 and 19 are 5-methylcytosines.
A method for delaying progression of prostatic tumor cells to an androgen-independent state, comprising treating androgen-sensitive prostatic tumor cells in vivo with an antisense oligonucleotide which inhibits expression of TRPM-2 by the tumor cells, wherein the antisense oligonucleotide has the sequence given by SEQ ID No. 4, wherein the oligonucleotide has a phosphorothioate backbone throughout, the sugar moieties of nucleotides 1-4 and 18-21 bear 2′-O-methoxyethyl modifications, and the remaining nucleotides (nucleotides 5-17) are 2′-deoxynucleotides, and wherein the cytosines of nucleotides 1, 4 and 19 are 5-methylcytosines.
A method for treating prostate cancer in an individual suffering from prostate cancer, comprising the steps of initiating androgen-withdrawal to induce apoptotic cell death of prostatic tumor cells in the individual, and administering to the individual a composition effective to inhibit expression of TRPM-2 by the tumor cells, thereby delaying the progression of prostatic tumor cells to an androgen-independent state in an individual, wherein the composition effective to inhibit expression of TRPM-2 is an antisense oligonucleotide, wherein the antisense oligonucleotide has the sequence given by SEQ ID No. 4, wherein the oligonucleotide has a phosphorothioate backbone throughout, the sugar moieties of nucleotides 1-4 and 18-21 bear 2′-O-methoxyethyl modifications, and the remaining nucleotides (nucleotides 5-17) are 2′-deoxynucleotides, and wherein the cytosines of nucleotides 1, 4 and 19 are 5-methylcytosines.
A method for enhancing the chemo- or radiation sensitivity of cancer cells in an individual suffering from a cancer that expresses TRPM-2 in amounts different from normal tissue of the same type, comprising administering to the individual a composition effective to inhibit expression of TRPM-2 by cancer cells, wherein the composition effective to inhibit expression of TRPM-2 is an antisense oligonucleotide, wherein the antisense oligonucleotide has the sequence given by SEQ ID No. 4, wherein the oligonucleotide has a phosphorothioate backbone throughout, the sugar moieties of nucleotides 1-4 and 18-21 bear 2′-O-methoxyethyl modifications, and the remaining nucleotides (nucleotides 5-17) are 2′-deoxynucleotides, and wherein the cytosines of nucleotides 1, 4 and 19 are 5-methylcytosines.
A method of delaying of progression of a population of prostatic tumor cells from a state in which living prostatic tumor cells are androgen-sensitive to a state in which living tumor cells are androgen independent, comprising treating the population of androgen-sensitive prostatic tumor cells with an antisense oligonucleotide which inhibits expression of TRPM-2 by the tumor cells, wherein the antisense oligonucleotide has the sequence given by SEQ ID No. 4, wherein the oligonucleotide has a phosphorothioate backbone throughout, the sugar moieties of nucleotides 1-4 and 18-21 bear 2′-O-methoxyethyl modifications, and the remaining nucleotides (nucleotides 5-17) are 2′-deoxynucleotides, and wherein the cytosines of nucleotides 1, 4 and 19 are 5-methylcytosines.
Dependencies are inferred from the claim text.