Tissue factor as a new target for CAR-NK cell immunotherapy of triple-negative breast cancer
Triple-negative breast cancer (TNBC), representing ~15% of globally diagnosed breast cancer, is typically an incurable malignancy due to the lack of targetable surface targets for development of effective therapy. To address the unmet need for TNBC treatment, we recently determined that tissue facto...
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description | Triple-negative breast cancer (TNBC), representing ~15% of globally diagnosed breast cancer, is typically an incurable malignancy due to the lack of targetable surface targets for development of effective therapy. To address the unmet need for TNBC treatment, we recently determined that tissue factor (TF) is a useful surface target in 50–85% of patients with TNBC and developed a second-generation TF-targeting antibody-like immunoconjugate (called L-ICON) for preclinical treatment of TNBC. Using the chimeric antigen receptor (CAR) approach, here we develop and test TF-targeting CAR-engineered natural killer (TF-CAR-NK) cells that co-express CD16, the Fc receptor (FcγIII) to mediate antibody-dependent cellular toxicity (ADCC), for a preclinical assessment of immunotherapy of TNBC using TF-CAR-NK cell as single agent therapy and in combination with L-ICON. Our preclinical results demonstrate that TF-CAR-NK cells alone could kill TNBC cells and its efficacy was enhanced with L-ICON ADCC
in vitro
. Moreover, TF-CAR-NK cells were effective
in vivo
for the treatment of TNBC in cell line- and patient’s tumor-derived xenograft mouse models. Thus, this study established the proof of concept of targeting TF as a new target in CAR-NK immunotherapy for effective treatment of TNBC and may warrant further preclinical study and potentially future investigation in TNBC patients. |
doi_str_mv | 10.1038/s41598-020-59736-3 |
format | Article |
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in vitro
. Moreover, TF-CAR-NK cells were effective
in vivo
for the treatment of TNBC in cell line- and patient’s tumor-derived xenograft mouse models. Thus, this study established the proof of concept of targeting TF as a new target in CAR-NK immunotherapy for effective treatment of TNBC and may warrant further preclinical study and potentially future investigation in TNBC patients.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-59736-3</identifier><identifier>PMID: 32071339</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13 ; 13/1 ; 13/106 ; 13/109 ; 42 ; 42/35 ; 631/250/251 ; 631/67/1347 ; 692/4028/67/580 ; Animal models ; Animals ; Breast cancer ; CD16 antigen ; Cell Line, Tumor ; Chimeric antigen receptors ; Cytotoxicity, Immunologic ; Fc receptors ; Female ; Humanities and Social Sciences ; Humans ; Immunotherapy ; Killer Cells, Natural - cytology ; Killer Cells, Natural - immunology ; Malignancy ; Mice ; multidisciplinary ; Natural killer cells ; Receptors, Chimeric Antigen - immunology ; Science ; Science (multidisciplinary) ; Thromboplastin - immunology ; Tissue factor ; Toxicity ; Triple Negative Breast Neoplasms - therapy ; Xenograft Model Antitumor Assays ; Xenografts</subject><ispartof>Scientific reports, 2020-02, Vol.10 (1), p.2815-2815, Article 2815</ispartof><rights>The Author(s) 2020</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-ba74423d63e5023437c35943e20feb4c9692c9175111f71052ca074535aae4a83</citedby><cites>FETCH-LOGICAL-c474t-ba74423d63e5023437c35943e20feb4c9692c9175111f71052ca074535aae4a83</cites><orcidid>0000-0002-0023-1170</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028910/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028910/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,41099,42168,51555,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32071339$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Zhiwei</creatorcontrib><title>Tissue factor as a new target for CAR-NK cell immunotherapy of triple-negative breast cancer</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Triple-negative breast cancer (TNBC), representing ~15% of globally diagnosed breast cancer, is typically an incurable malignancy due to the lack of targetable surface targets for development of effective therapy. To address the unmet need for TNBC treatment, we recently determined that tissue factor (TF) is a useful surface target in 50–85% of patients with TNBC and developed a second-generation TF-targeting antibody-like immunoconjugate (called L-ICON) for preclinical treatment of TNBC. Using the chimeric antigen receptor (CAR) approach, here we develop and test TF-targeting CAR-engineered natural killer (TF-CAR-NK) cells that co-express CD16, the Fc receptor (FcγIII) to mediate antibody-dependent cellular toxicity (ADCC), for a preclinical assessment of immunotherapy of TNBC using TF-CAR-NK cell as single agent therapy and in combination with L-ICON. Our preclinical results demonstrate that TF-CAR-NK cells alone could kill TNBC cells and its efficacy was enhanced with L-ICON ADCC
in vitro
. Moreover, TF-CAR-NK cells were effective
in vivo
for the treatment of TNBC in cell line- and patient’s tumor-derived xenograft mouse models. Thus, this study established the proof of concept of targeting TF as a new target in CAR-NK immunotherapy for effective treatment of TNBC and may warrant further preclinical study and potentially future investigation in TNBC patients.</description><subject>13</subject><subject>13/1</subject><subject>13/106</subject><subject>13/109</subject><subject>42</subject><subject>42/35</subject><subject>631/250/251</subject><subject>631/67/1347</subject><subject>692/4028/67/580</subject><subject>Animal models</subject><subject>Animals</subject><subject>Breast cancer</subject><subject>CD16 antigen</subject><subject>Cell Line, Tumor</subject><subject>Chimeric antigen receptors</subject><subject>Cytotoxicity, Immunologic</subject><subject>Fc receptors</subject><subject>Female</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Killer Cells, Natural - cytology</subject><subject>Killer Cells, Natural - immunology</subject><subject>Malignancy</subject><subject>Mice</subject><subject>multidisciplinary</subject><subject>Natural killer cells</subject><subject>Receptors, Chimeric Antigen - immunology</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Thromboplastin - immunology</subject><subject>Tissue factor</subject><subject>Toxicity</subject><subject>Triple Negative Breast Neoplasms - therapy</subject><subject>Xenograft Model Antitumor Assays</subject><subject>Xenografts</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1vVCEUhonR2GbsH3BhSNy4QYEDw2Vj0kz8io1NmrozIQw9d3qbe2EEbk3_vYxT--FCNhDOc154z0vIS8HfCg7du6KEth3jkjNtDSwZPCGHkivNJEj59MH5gByVcsXb0tIqYZ-TA5DcCAB7SH6cD6XMSHsfasrUF-ppxF-0-rzBSvt2tzo-Y9--0oDjSIdpmmOql5j99oamntY8bEdkETe-DtdI1xl9qTT4GDC_IM96PxY8ut0X5PvHD-erz-zk9NOX1fEJC8qoytbeKCXhYgmouQQFJoC2ClDyHtcq2KWVwQqjhRC9Ec1G8NwoDdp7VL6DBXm_193O6wkvAsaa_ei2eZh8vnHJD-5xJQ6XbpOuneGys22cC_LmViCnnzOW6qah7Az7iGkuToLutNF6KRv6-h_0Ks05Nns7yrT5CjCNknsq5FRKxv7uM4K7XX5un59r-bk_-TloTa8e2rhr-ZtWA2APlFaKG8z3b_9H9jeHmqSg</recordid><startdate>20200218</startdate><enddate>20200218</enddate><creator>Hu, Zhiwei</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0023-1170</orcidid></search><sort><creationdate>20200218</creationdate><title>Tissue factor as a new target for CAR-NK cell immunotherapy of triple-negative breast cancer</title><author>Hu, Zhiwei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-ba74423d63e5023437c35943e20feb4c9692c9175111f71052ca074535aae4a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>13</topic><topic>13/1</topic><topic>13/106</topic><topic>13/109</topic><topic>42</topic><topic>42/35</topic><topic>631/250/251</topic><topic>631/67/1347</topic><topic>692/4028/67/580</topic><topic>Animal models</topic><topic>Animals</topic><topic>Breast cancer</topic><topic>CD16 antigen</topic><topic>Cell Line, Tumor</topic><topic>Chimeric antigen receptors</topic><topic>Cytotoxicity, Immunologic</topic><topic>Fc receptors</topic><topic>Female</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Killer Cells, Natural - cytology</topic><topic>Killer Cells, Natural - immunology</topic><topic>Malignancy</topic><topic>Mice</topic><topic>multidisciplinary</topic><topic>Natural killer cells</topic><topic>Receptors, Chimeric Antigen - immunology</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Thromboplastin - immunology</topic><topic>Tissue factor</topic><topic>Toxicity</topic><topic>Triple Negative Breast Neoplasms - therapy</topic><topic>Xenograft Model Antitumor Assays</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Zhiwei</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Zhiwei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue factor as a new target for CAR-NK cell immunotherapy of triple-negative breast cancer</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-02-18</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>2815</spage><epage>2815</epage><pages>2815-2815</pages><artnum>2815</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Triple-negative breast cancer (TNBC), representing ~15% of globally diagnosed breast cancer, is typically an incurable malignancy due to the lack of targetable surface targets for development of effective therapy. To address the unmet need for TNBC treatment, we recently determined that tissue factor (TF) is a useful surface target in 50–85% of patients with TNBC and developed a second-generation TF-targeting antibody-like immunoconjugate (called L-ICON) for preclinical treatment of TNBC. Using the chimeric antigen receptor (CAR) approach, here we develop and test TF-targeting CAR-engineered natural killer (TF-CAR-NK) cells that co-express CD16, the Fc receptor (FcγIII) to mediate antibody-dependent cellular toxicity (ADCC), for a preclinical assessment of immunotherapy of TNBC using TF-CAR-NK cell as single agent therapy and in combination with L-ICON. Our preclinical results demonstrate that TF-CAR-NK cells alone could kill TNBC cells and its efficacy was enhanced with L-ICON ADCC
in vitro
. Moreover, TF-CAR-NK cells were effective
in vivo
for the treatment of TNBC in cell line- and patient’s tumor-derived xenograft mouse models. Thus, this study established the proof of concept of targeting TF as a new target in CAR-NK immunotherapy for effective treatment of TNBC and may warrant further preclinical study and potentially future investigation in TNBC patients.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32071339</pmid><doi>10.1038/s41598-020-59736-3</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0023-1170</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 13 13/1 13/106 13/109 42 42/35 631/250/251 631/67/1347 692/4028/67/580 Animal models Animals Breast cancer CD16 antigen Cell Line, Tumor Chimeric antigen receptors Cytotoxicity, Immunologic Fc receptors Female Humanities and Social Sciences Humans Immunotherapy Killer Cells, Natural - cytology Killer Cells, Natural - immunology Malignancy Mice multidisciplinary Natural killer cells Receptors, Chimeric Antigen - immunology Science Science (multidisciplinary) Thromboplastin - immunology Tissue factor Toxicity Triple Negative Breast Neoplasms - therapy Xenograft Model Antitumor Assays Xenografts |
title | Tissue factor as a new target for CAR-NK cell immunotherapy of triple-negative breast cancer |
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