Methods for in vivo identification of cancer initiating cells by multimodality reporter gene imaging
US-9220793-B2 · Dec 29, 2015 · US
US9072772B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9072772-B2 |
| Application number | US-201213463638-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 3, 2012 |
| Priority date | Nov 5, 2009 |
| Publication date | Jul 7, 2015 |
| Grant date | Jul 7, 2015 |
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The present invention relates to methods of treatment of clinical disorders associated with protein aggregation comprising administering, to a subject, an effective amount of an anti-protein aggregate (“APA”) compound selected from the group consisting of pimozide, fluphenazine (e.g., fluphenazine hydrochloride), tamoxifen (e.g., tamoxifen citrate), taxol, cantharidin, cantharidic acid, salts thereof and their structurally related compounds. It is based, at least in part, on the discovery that each of the aforelisted compounds were able to promote degradation of aggregated ATZ protein in a Caenorhabditis elegans model system. According to the invention, treatment with one or more of these APA compounds may be used to ameliorate the symptoms and signs of AT deficiency as well as other disorders marked by protein aggregation, including, but not limited to, Alzheimer's Disease, Parkinson's Disease, and Huntington's Disease.
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We claim: 1. A method of reducing aggregated ATZ protein in a subject suffering from α1-antitrypsin deficiency comprising administering, to the subject, an amount of fluphenazine effective in reducing aggregated ATZ protein.
containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone · CPC title
having four-membered rings, e.g. taxol · CPC title
Animal model, e.g. for test or diseases · CPC title
having six-membered rings, e.g. delta-lactones · CPC title
Screening agents using (non-human) animal models or transgenic animal models or chimeric hosts, e.g. Alzheimer disease animal model, transgenic model for heart failure · CPC title
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