Rna complexes and nanostructures for treatment of cancer metastasis
AssigneeOhio State Innovation Foundation
InventorsPeixuan GUO, Xin LI, Daniel BINZEL, Kai JIN
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Abstract
Disclosed herein are compositions and methods for one step CMC production of RNA therapeutic complexes (nanostructures) that contain nucleoside analogues. In some embodiments, the nucleoside analogues are incorporated into RNA oligonucleotides that self-assemble into an RNA complex during RNA synthesis in a one-step production. Therefore, no additional conjugation or synthesis processes are required.
Claims14
A therapeutic RNA complex comprising a plurality of synthetic double-stranded RNA oligonucleotides, each synthetic double-stranded RNA oligonucleotide comprising a sense strand and an antisense strand,
- wherein the sense strand has a 5′ end and a 3′ end with more than 25 nucleotides and a cholesterol molecule conjugated to the 3′ end of the sense strand, and the 2′-positions of all the pyrimidines at the sense strand do not contain oxygen,
- wherein the antisense strand has a 5′ end and a 3′ end with 18-25 normal nucleotides,
- wherein the sense strand is more than 18 nucleotides and the 2′-position of all the pyrimidine in the sense strand contain two fluorine and do not contain oxygen,
- wherein the antisense stand comprises an siRNA sequence with unmodified nucleotides,
- wherein the sense strand is the same length or longer than the antisense strand,
- wherein at least 95% of the nucleotides in the antisense strand are hybridized to complementary nucleotides of the sense strand, and
- wherein the plurality of synthetic double-stranded RNA oligonucleotides are in an aggregate with the cholesterol molecules at the center.
A synthetic double-stranded RNA oligonucleotide comprising a sense strand having a 5′ end and a 3′ end, an antisense siRNA strand having a 5′ end and a 3′ end, wherein the sense strand comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more floxuridine (5-fluorodeoxyuridine, UBSF) nucleotides, gemcitabine (2′, 2′-difluoro-2′-deoxycytidine, dFdC, CR2FF) nucleotides, or a combination thereof.
An RNA nanoparticle comprising at least three synthetic RNA nucleotides coupled to each other, wherein the at least three synthetic RNA oligonucleotides form a centrd no:al core domain and at least three double-stranded arms arranged around the core domain and extending away from the central core domain, and wherein at least one of the synthetic RNA oligonucleotides comprise a nucleic acid sequence selected from the group consisting of SEQ ID NOs:1-273, or a variant thereof having at least 90% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs:1-273.
A method for stabilizing an siRNA for therapeutic delivery, the method comprising
- (a) producing a plurality of synthetic single stranded RNA oligonucleotides complementary to the siRNA sequence, wherein each of the the RNA oligonucleotides comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more nucleoside analogs configured to prevent RNase degradation, and wherein each of the RNA oligonucleotides comprises a cholesterol moiety conjugated to its 3′ end, and
- (b) contacting the siRNA with the RNA oligonucleotides under conditions suitable to allow hybridization of the siRNA to the RNA oligonucleotides to produce a double-stranded RNA molecules that aggregate together with the cholesterol molecules at the center.
Dependencies are inferred from the claim text.