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
Hauptverfasser: Zhang, Lingjun, Fedorov, Yuriy, Adams, Drew, Lin, Feng
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container_title Molecular immunology
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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.
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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. 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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. 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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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