Identification of complement inhibitory activities of two chemotherapeutic agents using a high-throughput cell imaging-based screening assay
Excessive complement activation contributes significantly to the pathogeneses of various diseases. Currently, significant developmental research efforts aim to identify complement inhibitors with therapeutic uses have led to the approval of one inhibitor for clinical use. However, most existing comp...
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Veröffentlicht in: | Molecular immunology 2018-09, Vol.101, p.86-91 |
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creator | Zhang, Lingjun Fedorov, Yuriy Adams, Drew Lin, Feng |
description | Excessive complement activation contributes significantly to the pathogeneses of various diseases. Currently, significant developmental research efforts aim to identify complement inhibitors with therapeutic uses have led to the approval of one inhibitor for clinical use. However, most existing complement inhibitors are based on monoclonal antibodies, which have many drawbacks such as high costs and limited administration options. With this report, we establish an inexpensive, cell imaging-based high-throughput assay for the large-scale screening of potential small molecule complement inhibitors. Using this assay, we screened a library containing 3115 bioactive chemical compounds and identified cisplatin and pyridostatin as two new complement inhibitors in addition to nafamostat mesylate, a compound with known complement inhibitory activity. We further demonstrated that cisplatin and pyridostatin inhibit C5 convertases in the classical pathway of complement activation but have no effects on the alternative pathway of complement activation. In summary, this work has established a simple, large-scale, high-throughput assay for screening novel complement inhibitors and discovered previously unknown complement activation inhibitory activities for cisplatin and pyridostatin. |
doi_str_mv | 10.1016/j.molimm.2018.06.009 |
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Currently, significant developmental research efforts aim to identify complement inhibitors with therapeutic uses have led to the approval of one inhibitor for clinical use. However, most existing complement inhibitors are based on monoclonal antibodies, which have many drawbacks such as high costs and limited administration options. With this report, we establish an inexpensive, cell imaging-based high-throughput assay for the large-scale screening of potential small molecule complement inhibitors. Using this assay, we screened a library containing 3115 bioactive chemical compounds and identified cisplatin and pyridostatin as two new complement inhibitors in addition to nafamostat mesylate, a compound with known complement inhibitory activity. We further demonstrated that cisplatin and pyridostatin inhibit C5 convertases in the classical pathway of complement activation but have no effects on the alternative pathway of complement activation. In summary, this work has established a simple, large-scale, high-throughput assay for screening novel complement inhibitors and discovered previously unknown complement activation inhibitory activities for cisplatin and pyridostatin.</description><identifier>ISSN: 0161-5890</identifier><identifier>EISSN: 1872-9142</identifier><identifier>DOI: 10.1016/j.molimm.2018.06.009</identifier><identifier>PMID: 29909366</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Antineoplastic Agents - analysis ; Biological Assay - methods ; chemical compounds ; cisplatin ; Complement ; Complement C3 - antagonists & inhibitors ; Complement C3 - metabolism ; Complement C3-C5 Convertases - antagonists & inhibitors ; Complement C3-C5 Convertases - metabolism ; Complement Inactivating Agents - analysis ; complement inhibitor ; drug therapy ; Hemolysis - drug effects ; high-throughput ; High-Throughput Screening Assays - methods ; Image Processing, Computer-Assisted ; monoclonal antibodies ; Platinum - pharmacology ; Rabbits ; screening ; Sheep ; small compound ; Small Molecule Libraries - pharmacology</subject><ispartof>Molecular immunology, 2018-09, Vol.101, p.86-91</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-11db6077ebf3df72046e773f3cd008bff9f7f375049e68539eadd480a45a2a4a3</citedby><cites>FETCH-LOGICAL-c496t-11db6077ebf3df72046e773f3cd008bff9f7f375049e68539eadd480a45a2a4a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0161589018302013$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29909366$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Lingjun</creatorcontrib><creatorcontrib>Fedorov, Yuriy</creatorcontrib><creatorcontrib>Adams, Drew</creatorcontrib><creatorcontrib>Lin, Feng</creatorcontrib><title>Identification of complement inhibitory activities of two chemotherapeutic agents using a high-throughput cell imaging-based screening assay</title><title>Molecular immunology</title><addtitle>Mol Immunol</addtitle><description>Excessive complement activation contributes significantly to the pathogeneses of various diseases. Currently, significant developmental research efforts aim to identify complement inhibitors with therapeutic uses have led to the approval of one inhibitor for clinical use. However, most existing complement inhibitors are based on monoclonal antibodies, which have many drawbacks such as high costs and limited administration options. With this report, we establish an inexpensive, cell imaging-based high-throughput assay for the large-scale screening of potential small molecule complement inhibitors. Using this assay, we screened a library containing 3115 bioactive chemical compounds and identified cisplatin and pyridostatin as two new complement inhibitors in addition to nafamostat mesylate, a compound with known complement inhibitory activity. We further demonstrated that cisplatin and pyridostatin inhibit C5 convertases in the classical pathway of complement activation but have no effects on the alternative pathway of complement activation. In summary, this work has established a simple, large-scale, high-throughput assay for screening novel complement inhibitors and discovered previously unknown complement activation inhibitory activities for cisplatin and pyridostatin.</description><subject>Animals</subject><subject>Antineoplastic Agents - analysis</subject><subject>Biological Assay - methods</subject><subject>chemical compounds</subject><subject>cisplatin</subject><subject>Complement</subject><subject>Complement C3 - antagonists & inhibitors</subject><subject>Complement C3 - metabolism</subject><subject>Complement C3-C5 Convertases - antagonists & inhibitors</subject><subject>Complement C3-C5 Convertases - metabolism</subject><subject>Complement Inactivating Agents - analysis</subject><subject>complement inhibitor</subject><subject>drug therapy</subject><subject>Hemolysis - drug effects</subject><subject>high-throughput</subject><subject>High-Throughput Screening Assays - methods</subject><subject>Image Processing, Computer-Assisted</subject><subject>monoclonal antibodies</subject><subject>Platinum - pharmacology</subject><subject>Rabbits</subject><subject>screening</subject><subject>Sheep</subject><subject>small compound</subject><subject>Small Molecule Libraries - pharmacology</subject><issn>0161-5890</issn><issn>1872-9142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhSMEotPCGyDkJZuE6_zY8QYJVUArVWIDa8txrhOPkniwnUHzDn1oHKYU2MDKku851-f4y7JXFAoKlL3dF7Ob7DwXJdC2AFYAiCfZjra8zAWty6fZLslo3rQCLrLLEPYAwIA1z7OLUggQFWO77P62xyVaY7WK1i3EGaLdfJhwTtfELqPtbHT-RJSO9mijxbBp4ndH9IiziyN6dcA1Wk3UkDyBrMEuA1FktMOYx9G7dRgPayQap4nYWQ1pnHcqYE-C9ojLT3kI6vQie2bUFPDlw3mVff344cv1TX73-dPt9fu7XNeCxZzSvmPAOXam6g0voWbIeWUq3QO0nTHCcFPxBmqBrG0qgarv6xZU3ahS1aq6yt6d9x7WbsZep9heTfLgUzp_kk5Z-fdksaMc3FEyWrUNL9OCNw8LvPu2YohytmHrpxZ0a5BlIlRRwVOq_0qhYZxVbblJ67NUexeCR_OYiILcmMu9PDOXG3MJTCbmyfb6zzaPpl-Qf9fF9KdHi14GbXHR2FuPOsre2X-_8AMabsSl</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Zhang, Lingjun</creator><creator>Fedorov, Yuriy</creator><creator>Adams, Drew</creator><creator>Lin, Feng</creator><general>Elsevier Ltd</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>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20180901</creationdate><title>Identification of complement inhibitory activities of two chemotherapeutic agents using a high-throughput cell imaging-based screening assay</title><author>Zhang, Lingjun ; Fedorov, Yuriy ; Adams, Drew ; Lin, Feng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-11db6077ebf3df72046e773f3cd008bff9f7f375049e68539eadd480a45a2a4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - analysis</topic><topic>Biological Assay - methods</topic><topic>chemical compounds</topic><topic>cisplatin</topic><topic>Complement</topic><topic>Complement C3 - antagonists & inhibitors</topic><topic>Complement C3 - metabolism</topic><topic>Complement C3-C5 Convertases - antagonists & inhibitors</topic><topic>Complement C3-C5 Convertases - metabolism</topic><topic>Complement Inactivating Agents - analysis</topic><topic>complement inhibitor</topic><topic>drug therapy</topic><topic>Hemolysis - drug effects</topic><topic>high-throughput</topic><topic>High-Throughput Screening Assays - methods</topic><topic>Image Processing, Computer-Assisted</topic><topic>monoclonal antibodies</topic><topic>Platinum - pharmacology</topic><topic>Rabbits</topic><topic>screening</topic><topic>Sheep</topic><topic>small compound</topic><topic>Small Molecule Libraries - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Lingjun</creatorcontrib><creatorcontrib>Fedorov, Yuriy</creatorcontrib><creatorcontrib>Adams, Drew</creatorcontrib><creatorcontrib>Lin, Feng</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>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Lingjun</au><au>Fedorov, Yuriy</au><au>Adams, Drew</au><au>Lin, Feng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of complement inhibitory activities of two chemotherapeutic agents using a high-throughput cell imaging-based screening assay</atitle><jtitle>Molecular immunology</jtitle><addtitle>Mol Immunol</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>101</volume><spage>86</spage><epage>91</epage><pages>86-91</pages><issn>0161-5890</issn><eissn>1872-9142</eissn><abstract>Excessive complement activation contributes significantly to the pathogeneses of various diseases. Currently, significant developmental research efforts aim to identify complement inhibitors with therapeutic uses have led to the approval of one inhibitor for clinical use. However, most existing complement inhibitors are based on monoclonal antibodies, which have many drawbacks such as high costs and limited administration options. With this report, we establish an inexpensive, cell imaging-based high-throughput assay for the large-scale screening of potential small molecule complement inhibitors. Using this assay, we screened a library containing 3115 bioactive chemical compounds and identified cisplatin and pyridostatin as two new complement inhibitors in addition to nafamostat mesylate, a compound with known complement inhibitory activity. We further demonstrated that cisplatin and pyridostatin inhibit C5 convertases in the classical pathway of complement activation but have no effects on the alternative pathway of complement activation. In summary, this work has established a simple, large-scale, high-throughput assay for screening novel complement inhibitors and discovered previously unknown complement activation inhibitory activities for cisplatin and pyridostatin.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>29909366</pmid><doi>10.1016/j.molimm.2018.06.009</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic Agents - analysis Biological Assay - methods chemical compounds cisplatin Complement Complement C3 - antagonists & inhibitors Complement C3 - metabolism Complement C3-C5 Convertases - antagonists & inhibitors Complement C3-C5 Convertases - metabolism Complement Inactivating Agents - analysis complement inhibitor drug therapy Hemolysis - drug effects high-throughput High-Throughput Screening Assays - methods Image Processing, Computer-Assisted monoclonal antibodies Platinum - pharmacology Rabbits screening Sheep small compound Small Molecule Libraries - pharmacology |
title | Identification of complement inhibitory activities of two chemotherapeutic agents using a high-throughput cell imaging-based screening assay |
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