Treatment of Liver Diseases With Cell Death Inducing DFFA Like Effector B (CIDEB) Inhibitors
US-2024376471-A1 · Nov 14, 2024 · US
US9260717B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9260717-B2 |
| Application number | US-201214115730-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 20, 2012 |
| Priority date | Aug 24, 2011 |
| Publication date | Feb 16, 2016 |
| Grant date | Feb 16, 2016 |
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The present invention relates to a method of screening for modulator of chaperonin that is involved in protein aggregation inducing neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease and Huntington's disease, use of the chaperonin modulator screened by the method for prevention and treatment of neurodegenerative diseases. According to the present invention, novel negative chaperonin modulator is provided, and chaperonin modulator may be more rapidly and conveniently screened with the negative modulator as a target. Furthermore, by using the screened material, neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease and Huntington's disease may be effectively prevented or treated without concern for cell death due to autophagy, which is the existing method of removing protein aggregate.
Opening claim text (preview).
The invention claimed is: 1. A method of screening for a CCT4 modulator, the method comprising 1) preparing a candidate material and VRK2; 2) measuring an expression amount or a kinase activity of the VRK2; 3) treating the VRK2 with the candidate material and measuring a change in the expression amount or the kinase activity of the VRK2; and 4) determining the candidate material as the CCT4 modulator by comparing the expression amount or the kinase activity of VRK2 between the treated and untreated groups. 2. The method according to claim 1 , wherein the CCT4 modulator increases an expression amount or a stability of CCT4 protein, and the step 4) is performed by identifying the candidate material as a material that increases the expression amount or the stability of CCT4 protein if the expression amount or the kinase activity of VRK2 is decreased compared to untreated group. 3. The method according to claim 1 , wherein the CCT4 modulator decreases an expression amount or a stability of CCT4 protein, and the step 4) is performed by identifying the candidate material as a material that decreases the expression amount or stability of CCT4 protein if the expression amount or the kinase activity of VRK2 is increased compared to untreated group.
for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia · CPC title
for treating abnormal movements, e.g. chorea, dyskinesia · CPC title
Anti-Parkinson drugs · CPC title
against enzymes (viral enzymes C12N15/1131; receptors C12N15/1138) · CPC title
miRNA, siRNA or ncRNA · CPC title
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