IP Library Granted Patent US 11,920,195
Granted Patent B2
US 11,920,195 · App. 17/334,345 · Granted Mar 5, 2024

Method for diagnosing drug addiction, method for screening therapeutic agent for drug addiction and pharmaceutical composition for preventing or treating drug addiction

Inventors: Heh-In Im (Seoul, KR); Baek Sun Kim (Seoul, KR); Sung Hyun Tag (Seoul, KR)
Assignee: Korea Institute of Science and Technology
C12Q1/6876C12Q1/686C12Q2600/178
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Quick Facts
Patent No.
US 11,920,195
App. No.
17/334,345
Granted
Mar 5, 2024
Kind
B2
Abstract

Disclosed is a composition for diagnosing, preventing or treating drug addiction based on synaptotagmin binding cytoplasmic RNA interacting protein (SYNCRIP). SYNCRIP or a gene encoding the protein can be used to diagnose drug addiction. In addition, a therapeutic agent for drug addiction can be discovered by measuring the expression of SYNCRIP. Furthermore, an agent expressing SYNCRIP or promoting the activity of SYNCRIP can be used to prevent or treat drug addiction.

Claims (7)

1. A method for screening a therapeutic agent for drug addiction, comprising a) inducing drug addiction in an animal and treating the drug-addicted animal or a biological sample separated therefrom with a candidate agent; b) measuring the synaptotagmin binding cytoplasmic RNA interacting protein (SYNCRIP) gene or its expression level in the candidate agent-treated animal or biological sample, and c) selecting the candidate agent as a therapeutic agent for drug addiction if the measured expression level of the SYNCRIP gene is higher than that in a control group untreated with the candidate agent.

2. The method according to claim 1 , wherein the SYNCRIP gene has the sequence set forth in SEQ ID NO: 1.

3. The method according to claim 1 , wherein the expression level is measured using a technique selected from the group consisting of polymerase chain reaction (PCR), quantitative polymerase chain reaction (qPCR), reverse transcription polymerase chain reaction (RT-PCR), competitive reverse transcription polymerase chain reaction (competitive RT-PCR), quantitative real-time polymerase chain reaction (qRT-PCR), real-time reverse transcription polymerase chain reaction (real-time RT-PCR), RNase protection assay, Northern blot analysis, and DNA chip analysis.

4. The method according to claim 1 , further comprising measuring the expression level of miR-137 in the serum of the candidate agent-treated animal.

5. A method for diagnosing or treating drug addiction, comprising a) measuring the synaptotagmin binding cytoplasmic RNA interacting protein (SYNCRIP) gene or its expression level in a biological sample separated from a subject, b) diagnosing the subject as having drug addiction if the measured expression level of the SYNCRIP gene is higher than that in a normal control group, and c) administering an agent expressing SYNCRIP or promoting the activity of SYNCRIP to the subject diagnosed as having drug addiction.

6. The method according to claim 5 , wherein the SYNCRIP gene has the sequence set forth in SEQ ID NO: 1.

7. The method according to claim 5 , wherein the expression level is measured using a technique selected from the group consisting of polymerase chain reaction (PCR), quantitative polymerase chain reaction (qPCR), reverse transcription polymerase chain reaction (RT-PCR), competitive reverse transcription polymerase chain reaction (competitive RT-PCR), quantitative real-time polymerase chain reaction (qRT-PCR), real-time reverse transcription polymerase chain reaction (real-time RT-PCR), RNase protection assay, Northern blot analysis, and DNA chip analysis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2024
From: KIM, BAEK SUN
To: KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY
Reel/Frame 066635/0514 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2021
From: IM, HEH-IN; KIM, BYUNG SUN; TAG, SUNG HYUN
To: KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY
Reel/Frame 056388/0334 →
Priority Claims (2)
KR 10-2020-0077727 · Jun 25, 2020 · national
KR 10-2021-0047804 · Apr 13, 2021 · national
Continuity (1)
Related Publication 20210403996A1 · Dec 30, 2021