Nucleolin specific aptamer and use thereof
View Patent ↗Improved G-rich oligonucleotide (GRO) aptamers specific to nucleolin, a method of preparing the aptamers, and a use of the aptamers for diagnosing and/or treating a nucleolin-associated disease, are provided.
1. Nucleolin-specific aptamer, wherein the aptamer has the sequence of SEQ ID NO: 3, and two thymidines(T) present at at least 12 th and 13 th positions of the nucleotide sequence are independently substituted with a modified pyrimidine nucleoside, and wherein the modified pyrimidine nucleoside is deoxyuridine(dU), deoxycytidine(dC), uridine(U), or cytidine(C) having a hydrophobic group at 5 position:
NGGTGGTGGTGGTTGTGGTGGTGGTGGN
(SEQ ID NO: 3)
wherein each N is absent or 1 to 20 nucleosides, which is independently selected from the group consisting of adenosine(A), thymidine(T)/uridine(U), cytidine(C), and guanosine(G), and the positions are counted starting from ‘G’ immediately following ‘N’ at 5′-end,
wherein the hydrophobic group is selected from the group consisting of a benzyl group, a naphthyl group, or a pyrrolebenzyl group.
2. The nucleolin-specific aptamer according to claim 1 , wherein the aptamer has the sequence of SEQ ID NO: 1 or 2, and two thymidines(T) present at at least 15 th and 16 th positions of SEQ ID NO: 1 or at least 12 th and 13 th positions of SEQ ID NO: 2 are independently substituted with a modified pyrimidine nucleoside, and wherein the modified pyrimidine nucleoside is deoxyuridine(dU), deoxycytidine(dC), uridine(U), or cytidine(C) having a hydrophobic group at 5 position.
3. The nucleolin-specific aptamer according to claim 1 , wherein the modified pyrimidine nucleoside is selected from the group consisting of 5-(N-benzylcarboxyamide)-2′-deoxyuridine(called BzdU), 5-(N-naphthylcarboxyamide)-2′-deoxyuridine(called NapdU), 5-(N-4-pyrrolebenzylcarboxyamide)-2′-deoxyuridine(called 4-PBdU), 5-(N-benzylcarboxyamide)-2′-deoxycytidine (called BzdC), 5-(N- naphthylcarboxyamide)-2′-deoxycytidine (called NapdC), 5-(N-4-pyrrolebenzylcarboxyamide)-2′-deoxycytidine (called 4-PBdC), 5-(N-benzylcarboxyamide)-2′-uridine(called BzU), 5-(N-naphthylcarboxyamide)-2′-uridine(called NapU), 5-(N-4-pyrrolebenzylcarboxyamide)-2′-uridine(called 4-PBU), 5-(N-benzylcarboxyamide)-2′-cytidine (called BzC), 5-(N-naphthylcarboxyamide)-2′-cytidine (called NapC), and 5-(N-4-pyrrolebenzylcarboxyamide)-2′-cytidine (called 4-PBC).
4. The nucleolin-specific aptamer according to claim 1 , wherein at least one thymidine in addition to the two thymidines(T) present at 12 th and 13 th positions of SEQ ID NO: 3 are additionally substituted with the modified pyrimidine nucleoside, and the positions are counted starting from ‘G’ immediately following ‘N’ at 5′-end.
5. The nucleolin-specific aptamer according to claim 2 , wherein at least one thymidine in addition to the two thymidines(T) present at 15 th and 16 th positions of SEQ ID NO: 1 or 12 th and 13 th positions of SEQ ID NO: 2 are additionally substituted with the modified pyrimidine nucleoside, myeloproliferative disorders, carcinomas of solid tissue, sarcomas, melanomas, adenomas, hypoxic tumors, squamous cell carcinomas of the mouth, throat, larynx, or lung, genitourinary cancers, hematopoietic cancers, head and neck cancers, and nervous system cancers, and benign lesions.
6. A pharmaceutical composition containing the nucleolin-specific aptamer of claim 1 .
7. A method of inhibiting nucleolin, comprising the step of administering the nucleolin-specific aptamer of claim 1 to a subject or a sample comprising nucleolin-expressing cells.
8. A method of inhibiting hyperproliferation of cell cased by nucleolin, comprising the step of administering the nucleolin-specific aptamer of claim 1 to a subject or a sample comprising nucleolin-expressing cells.