Progesterone Receptor Chaperone Complex–Based High-Throughput Screening Assay: Identification of Capsaicin as an Inhibitor of the Hsp90 Machine
Hsp90 and its co-chaperones are known to be important for cancer cell survival. The N-terminal inhibitors of Hsp90 that are in ongoing clinical trials as antitumor agents have unfortunately shown disappointing efficacies in the clinic. Thus, novel inhibitors of the Hsp90 machine with a different mec...
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Veröffentlicht in: | Journal of biomolecular screening 2015-02, Vol.20 (2), p.223-229 |
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creator | Patwardhan, Chaitanya A. Alfa, Eyad Lu, Su Chadli, Ahmed |
description | Hsp90 and its co-chaperones are known to be important for cancer cell survival. The N-terminal inhibitors of Hsp90 that are in ongoing clinical trials as antitumor agents have unfortunately shown disappointing efficacies in the clinic. Thus, novel inhibitors of the Hsp90 machine with a different mechanism of action are urgently needed. We report here the development of a novel high-throughput screening assay platform to identify small-molecule inhibitors of Hsp90 and its co-chaperones. This assay quantitatively measures the ability of Hsp90 and its co-chaperones to refold/protect the progesterone receptor, a physiological client of Hsp90, in a 96-well plate format. We screened the National Institutes of Health clinical collection drug library and identified capsaicin as a hit molecule. Capsaicin is a Food and Drug Administration–approved drug for topical use in pain management. Cell survival assays showed that capsaicin selectively kills cancer cells and destabilizes several Hsp90 client proteins. Thus, our data may explain the seemingly pleotropic effect of capsaicin. |
doi_str_mv | 10.1177/1087057114549147 |
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The N-terminal inhibitors of Hsp90 that are in ongoing clinical trials as antitumor agents have unfortunately shown disappointing efficacies in the clinic. Thus, novel inhibitors of the Hsp90 machine with a different mechanism of action are urgently needed. We report here the development of a novel high-throughput screening assay platform to identify small-molecule inhibitors of Hsp90 and its co-chaperones. This assay quantitatively measures the ability of Hsp90 and its co-chaperones to refold/protect the progesterone receptor, a physiological client of Hsp90, in a 96-well plate format. We screened the National Institutes of Health clinical collection drug library and identified capsaicin as a hit molecule. Capsaicin is a Food and Drug Administration–approved drug for topical use in pain management. Cell survival assays showed that capsaicin selectively kills cancer cells and destabilizes several Hsp90 client proteins. Thus, our data may explain the seemingly pleotropic effect of capsaicin.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Capsaicin - pharmacology</subject><subject>Drug Discovery - methods</subject><subject>Drug Screening Assays, Antitumor - methods</subject><subject>High-Throughput Screening Assays - methods</subject><subject>HSP90 Heat-Shock Proteins - antagonists & inhibitors</subject><subject>Humans</subject><subject>Molecular Chaperones - metabolism</subject><subject>Protein Binding</subject><subject>Receptors, Progesterone - antagonists & inhibitors</subject><subject>Receptors, Progesterone - chemistry</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Reproducibility of Results</subject><subject>Small Molecule Libraries</subject><issn>1087-0571</issn><issn>2472-5552</issn><issn>1552-454X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkL9OwzAQxi0EoqWwM6GMLAE7tmNnLBFQpEpFUCS2yEkvaaskDnYi0Y134A15ElxSGJCQmO7f7z7dfQidEnxBiBCXBEuBuSCEcRYRJvbQkHAe-K583ne5G_vb-QAdWbvGmNAQs0M0CDiRjBM2RLN7owuwLRhdg_cAGTStNl68VE3finXVlPD68fZ-pSwsvMmqWPrzpdFdsWy61nvMDEC9qgtvbK3aHKODXJUWTnZxhJ5urufxxJ_Obu_i8dTPGJWtH6YcFkoq4Cpi2J0pcwxUhhJCJQIRAc8AJFUBV5wCiVIJEYtEmBOKaZoBHaHzXrcx-qVzDyTVymZQlqoG3dmEhO5TLMIo-gfKA4ap-EJxj2ZGW2sgTxqzqpTZJAQnW8eT3467lbOdepdWsPhZ-LbYAX4PWFVAstadqZ0xfwt-AtyTiMI</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Patwardhan, Chaitanya A.</creator><creator>Alfa, Eyad</creator><creator>Lu, Su</creator><creator>Chadli, Ahmed</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20150201</creationdate><title>Progesterone Receptor Chaperone Complex–Based High-Throughput Screening Assay</title><author>Patwardhan, Chaitanya A. ; Alfa, Eyad ; Lu, Su ; Chadli, Ahmed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-6b5eda8ae5a9400878f0e3868e6a7279e5cee83a25a53e19b8e94976f1303bce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Capsaicin - pharmacology</topic><topic>Drug Discovery - methods</topic><topic>Drug Screening Assays, Antitumor - methods</topic><topic>High-Throughput Screening Assays - methods</topic><topic>HSP90 Heat-Shock Proteins - antagonists & inhibitors</topic><topic>Humans</topic><topic>Molecular Chaperones - metabolism</topic><topic>Protein Binding</topic><topic>Receptors, Progesterone - antagonists & inhibitors</topic><topic>Receptors, Progesterone - chemistry</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Reproducibility of Results</topic><topic>Small Molecule Libraries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patwardhan, Chaitanya A.</creatorcontrib><creatorcontrib>Alfa, Eyad</creatorcontrib><creatorcontrib>Lu, Su</creatorcontrib><creatorcontrib>Chadli, Ahmed</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of biomolecular screening</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patwardhan, Chaitanya A.</au><au>Alfa, Eyad</au><au>Lu, Su</au><au>Chadli, Ahmed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progesterone Receptor Chaperone Complex–Based High-Throughput Screening Assay: Identification of Capsaicin as an Inhibitor of the Hsp90 Machine</atitle><jtitle>Journal of biomolecular screening</jtitle><addtitle>J Biomol Screen</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>20</volume><issue>2</issue><spage>223</spage><epage>229</epage><pages>223-229</pages><issn>1087-0571</issn><issn>2472-5552</issn><eissn>1552-454X</eissn><abstract>Hsp90 and its co-chaperones are known to be important for cancer cell survival. The N-terminal inhibitors of Hsp90 that are in ongoing clinical trials as antitumor agents have unfortunately shown disappointing efficacies in the clinic. Thus, novel inhibitors of the Hsp90 machine with a different mechanism of action are urgently needed. We report here the development of a novel high-throughput screening assay platform to identify small-molecule inhibitors of Hsp90 and its co-chaperones. This assay quantitatively measures the ability of Hsp90 and its co-chaperones to refold/protect the progesterone receptor, a physiological client of Hsp90, in a 96-well plate format. We screened the National Institutes of Health clinical collection drug library and identified capsaicin as a hit molecule. Capsaicin is a Food and Drug Administration–approved drug for topical use in pain management. Cell survival assays showed that capsaicin selectively kills cancer cells and destabilizes several Hsp90 client proteins. 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subjects | Animals Antineoplastic Agents - pharmacology Capsaicin - pharmacology Drug Discovery - methods Drug Screening Assays, Antitumor - methods High-Throughput Screening Assays - methods HSP90 Heat-Shock Proteins - antagonists & inhibitors Humans Molecular Chaperones - metabolism Protein Binding Receptors, Progesterone - antagonists & inhibitors Receptors, Progesterone - chemistry Receptors, Progesterone - metabolism Reproducibility of Results Small Molecule Libraries |
title | Progesterone Receptor Chaperone Complex–Based High-Throughput Screening Assay: Identification of Capsaicin as an Inhibitor of the Hsp90 Machine |
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