Potent LNA oligonucleotides for the inhibition of HIF-1a expression
View Patent ↗The present disclosure relates to an LNA oligonucleotide consisting of a sequence selected from the group consisting of 5′-( T x )G x G x c s a s a s g s c s a s t s c s c s T x G x T -3′ and 5′-( G x )T x T x a s c s t s g s c s c s t s t s c s T x T x A -3′, wherein capital letters designate a beta-D-oxy-LNA nucleotide analogue, small letters designate a 2-deoxynucleotide, underline designates either a beta-D-oxy-LNA nucleotide analogue or a 2-deoxynucleotide, subscript “s” designates a phosphorothioate link between neighbouring nucleotides/LNA nucleotide analogues, and subscript “x” designates either a phosphorothioate link or a phosphorodiester link between neighbouring nucleotides/LNA nucleotide analogues, and wherein the sequence is optionally extended by up to five 2-deoxynucleotide units. The LNA oligonucleotides are useful for modulating the expression of hypoxia-inducible factor-1a (HIF-1a), e.g. in the treatment of cancer diseases, inhibiting angiogenesis, inducing apoptosis, preventing cellular proliferation, or treating an angiogenic disease, e.g. diabetic retinopathy, macular degeneration (ARMD), psoriasis, rheumatoid arthritis and other inflammatory diseases.
1. A method for treating cancer, said method comprising administering a therapeutically effective amount of an LNA oligonucleotide consisting of the sequence:
5′-T s G s G s c s a s a s g s c s a s t s c s c s T s G s T s a-3′ (SEQ ID NO. 1)
wherein capital letters designate a beta-D-oxy-LNA nucleotide analogue, lower case letters designate a 2-deoxynucleotide, and subscript “s” designates a phosphorothioate link between neighboring nucleotides/LNA nucleotide analogues to a patient in need thereof.
2. The method according to claim 1 , wherein said cancer is a solid tumor.
3. The method according to claim 1 , wherein the cancer is selected from the group consisting of multiple myeloma, renal cancer, cervical cancer, colon cancer, brain cancer, and breast cancer.
4. A method of inducing apoptosis in a cell comprising contacting the cell with an effective amount of an LNA oligonucleotide consisting of the sequence:
5′-T s G s G s c s a s a s g s c s a s t s c s c s T s G s T s a-3′ (SEQ ID NO. 1)
wherein capital letters designate a beta-D-oxy-LNA nucleotide analogue, lower case letters designate a 2-deoxynucleotide, and subscript “s” designates a phosphorothioate link between neighboring nucleotides/LNA nucleotide analogues.
5. A method of preventing proliferation of a cell comprising contacting the cell with an effective amount of an LNA oligonucleotide consisting of the sequence:
5′-T s G s G s c s a s a s g s c s a s t s c s c s T s G s T s a-3′ (SEQ ID NO. 1)
wherein capital letters designate a beta-D-oxy-LNA nucleotide analogue, lower case letters designate a 2-deoxynucleotide, and subscript “s” designates a phosphorothioate link between neighboring nucleotides/LNA nucleotide analogues.