Methods of Treating Disorders Associated with Protein Aggregation

Abstract

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.

Description

PRIORITY[0001]This application is a continuation of International Patent Application Serial No. PCT / US2010 / 002898 filed Nov. 4, 2010 and claims priority to U.S. Provisional Application No. 61 / 258,384 filed Nov. 5, 2009, U.S. Provisional Application No. 61 / 382,796 filed Sep. 14, 2010, and U.S. Ser. No. 12 / 881,976 filed Sep. 14, 2010, the contents of each of which are hereby incorporated by reference in their entireties herein.GRANT INFORMATION[0002]This invention was made with government support under grant DK079806 awarded by the National Institutes of Health. The government has certain rights in the invention.1. INTRODUCTION[0003]The present invention relates to methods of treating 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, tamoxifen, taxol, cantharidin, cantharidic acid, salts thereof, and their structur...

AI Technical Summary

Benefits of technology

The patent relates to a method and composition for screening drugs in C. elegans to treat disorders associated with protein aggregation. A special genetic modification is used to create a model system for these disorders. The method utilizes a high throughput screening system and takes advantage of the advantages of C. elegans in in vivo high-speed drug discovery campaigns. The method involves automating the image acquisition and data analysis components to accurately define objects and detect tissue-specific changes using fluorescent markers. The invention overcomes a bottleneck in the screening process and enables monitoring complex physiological processes and screening for drugs that modulate these processes.

Problems solved by technology

Individuals who are homozygous for the mutant allele are susceptible to premature development of chronic obstructive pulmonary disease.

Thus, based on the current literature, autophagy may be increased in AD, but the load of oligomers may be too great to avoid toxic Aβ accumulation.

Huntington's Chorea is associated with aggregates of huntingtin protein containing a mutation that results in long tracts of polyglutamine (“polyQ”) which result in improper protein processing and aggregate formation.

Despite these advances, a lead series painstakingly developed in vitro may be abandoned due to the loss of activity or an unfavorable therapeutic index upon testing in mammalian cell cultures, vertebrate animals or phase 1 clinical trials (60, 61).

Initially, however, cell-based screening systems suffered from a lack of assay robustness, intensive labor and resource utilization, and low throughput; especially in terms of data acquisition, storage and analysis.

While HCS using cell-based assays facilitate the elimination of compounds that are directly cytotoxic, they are unable to identify those that lose their desired therapeutic effect in vivo, or demonstrate deleterious side effects on complex developmental or physiological processes, such as cellular migration or synaptic transmission, respectively.

Despite these advantages, the assimilation of live animals into drug screening protocols presents logistical challenges.

These barriers include labor- and cost-intensive development of suitable disease phenotypes; screening protocols that are low-throughput and unamenable to statistically robust HCS-like formats; and the prohibitive consumption of compound libraries.

Nonetheless, experimental variables that affect high-quality HCS protocols, such as sample preparation, assay strategy, and image acquisition, have yet to be optimized for any organism (77).

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