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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of biomolecular screening 2015-02, Vol.20 (2), p.223-229
Hauptverfasser: Patwardhan, Chaitanya A., Alfa, Eyad, Lu, Su, Chadli, Ahmed
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 229
container_issue 2
container_start_page 223
container_title Journal of biomolecular screening
container_volume 20
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1177_1087057114549147</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1087057114549147</sage_id><sourcerecordid>1660407699</sourcerecordid><originalsourceid>FETCH-LOGICAL-c438t-6b5eda8ae5a9400878f0e3868e6a7279e5cee83a25a53e19b8e94976f1303bce3</originalsourceid><addsrcrecordid>eNqNkL9OwzAQxi0EoqWwM6GMLAE7tmNnLBFQpEpFUCS2yEkvaaskDnYi0Y134A15ElxSGJCQmO7f7z7dfQidEnxBiBCXBEuBuSCEcRYRJvbQkHAe-K583ne5G_vb-QAdWbvGmNAQs0M0CDiRjBM2RLN7owuwLRhdg_cAGTStNl68VE3finXVlPD68fZ-pSwsvMmqWPrzpdFdsWy61nvMDEC9qgtvbK3aHKODXJUWTnZxhJ5urufxxJ_Obu_i8dTPGJWtH6YcFkoq4Cpi2J0pcwxUhhJCJQIRAc8AJFUBV5wCiVIJEYtEmBOKaZoBHaHzXrcx-qVzDyTVymZQlqoG3dmEhO5TLMIo-gfKA4ap-EJxj2ZGW2sgTxqzqpTZJAQnW8eT3467lbOdepdWsPhZ-LbYAX4PWFVAstadqZ0xfwt-AtyTiMI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1652403799</pqid></control><display><type>article</type><title>Progesterone Receptor Chaperone Complex–Based High-Throughput Screening Assay: Identification of Capsaicin as an Inhibitor of the Hsp90 Machine</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Patwardhan, Chaitanya A. ; Alfa, Eyad ; Lu, Su ; Chadli, Ahmed</creator><creatorcontrib>Patwardhan, Chaitanya A. ; Alfa, Eyad ; Lu, Su ; Chadli, Ahmed</creatorcontrib><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.</description><identifier>ISSN: 1087-0571</identifier><identifier>ISSN: 2472-5552</identifier><identifier>EISSN: 1552-454X</identifier><identifier>DOI: 10.1177/1087057114549147</identifier><identifier>PMID: 25184514</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Capsaicin - pharmacology ; Drug Discovery - methods ; Drug Screening Assays, Antitumor - methods ; High-Throughput Screening Assays - methods ; HSP90 Heat-Shock Proteins - antagonists &amp; inhibitors ; Humans ; Molecular Chaperones - metabolism ; Protein Binding ; Receptors, Progesterone - antagonists &amp; inhibitors ; Receptors, Progesterone - chemistry ; Receptors, Progesterone - metabolism ; Reproducibility of Results ; Small Molecule Libraries</subject><ispartof>Journal of biomolecular screening, 2015-02, Vol.20 (2), p.223-229</ispartof><rights>2014 Society for Laboratory Automation and Screening</rights><rights>2014 Society for Laboratory Automation and Screening.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-6b5eda8ae5a9400878f0e3868e6a7279e5cee83a25a53e19b8e94976f1303bce3</citedby><cites>FETCH-LOGICAL-c438t-6b5eda8ae5a9400878f0e3868e6a7279e5cee83a25a53e19b8e94976f1303bce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25184514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Patwardhan, Chaitanya A.</creatorcontrib><creatorcontrib>Alfa, Eyad</creatorcontrib><creatorcontrib>Lu, Su</creatorcontrib><creatorcontrib>Chadli, Ahmed</creatorcontrib><title>Progesterone Receptor Chaperone Complex–Based High-Throughput Screening Assay: Identification of Capsaicin as an Inhibitor of the Hsp90 Machine</title><title>Journal of biomolecular screening</title><addtitle>J Biomol Screen</addtitle><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.</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 &amp; inhibitors</subject><subject>Humans</subject><subject>Molecular Chaperones - metabolism</subject><subject>Protein Binding</subject><subject>Receptors, Progesterone - antagonists &amp; 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 &amp; inhibitors</topic><topic>Humans</topic><topic>Molecular Chaperones - metabolism</topic><topic>Protein Binding</topic><topic>Receptors, Progesterone - antagonists &amp; 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. Thus, our data may explain the seemingly pleotropic effect of capsaicin.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>25184514</pmid><doi>10.1177/1087057114549147</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1087-0571
ispartof Journal of biomolecular screening, 2015-02, Vol.20 (2), p.223-229
issn 1087-0571
2472-5552
1552-454X
language eng
recordid cdi_crossref_primary_10_1177_1087057114549147
source MEDLINE; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T01%3A04%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Progesterone%20Receptor%20Chaperone%20Complex%E2%80%93Based%20High-Throughput%20Screening%20Assay:%20Identification%20of%20Capsaicin%20as%20an%20Inhibitor%20of%20the%20Hsp90%20Machine&rft.jtitle=Journal%20of%20biomolecular%20screening&rft.au=Patwardhan,%20Chaitanya%20A.&rft.date=2015-02-01&rft.volume=20&rft.issue=2&rft.spage=223&rft.epage=229&rft.pages=223-229&rft.issn=1087-0571&rft.eissn=1552-454X&rft_id=info:doi/10.1177/1087057114549147&rft_dat=%3Cproquest_cross%3E1660407699%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1652403799&rft_id=info:pmid/25184514&rft_sage_id=10.1177_1087057114549147&rfr_iscdi=true