A monomethyl auristatin E-conjugated antibody to guanylyl cyclase C is cytotoxic to target-expressing cells in vitro and in vivo

Guanylyl cyclase C (GCC) is a cell-surface protein that is expressed by normal intestinal epithelial cells, more than 95% of metastatic colorectal cancers (mCRC), and the majority of gastric and pancreatic cancers. Due to strict apical localization, systemically delivered GCC-targeting agents should...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2018-01, Vol.13 (1), p.e0191046-e0191046
Hauptverfasser: Gallery, Melissa, Zhang, Julie, Bradley, Daniel P, Brauer, Pamela, Cvet, Donna, Estevam, Jose, Danaee, Hadi, Greenfield, Edward, Li, Ping, Manfredi, Mark, Loke, Huay-Keng, Rabino, Claudia, Stringer, Brad, Williamson, Mark, Wyant, Tim, Yang, Johnny, Zhu, Qing, Abu-Yousif, Adnan, Veiby, O Petter
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e0191046
container_issue 1
container_start_page e0191046
container_title PloS one
container_volume 13
creator Gallery, Melissa
Zhang, Julie
Bradley, Daniel P
Brauer, Pamela
Cvet, Donna
Estevam, Jose
Danaee, Hadi
Greenfield, Edward
Li, Ping
Manfredi, Mark
Loke, Huay-Keng
Rabino, Claudia
Stringer, Brad
Williamson, Mark
Wyant, Tim
Yang, Johnny
Zhu, Qing
Abu-Yousif, Adnan
Veiby, O Petter
description Guanylyl cyclase C (GCC) is a cell-surface protein that is expressed by normal intestinal epithelial cells, more than 95% of metastatic colorectal cancers (mCRC), and the majority of gastric and pancreatic cancers. Due to strict apical localization, systemically delivered GCC-targeting agents should not reach GCC in normal intestinal tissue, while accessing antigen in tumor. We generated an investigational antibody-drug conjugate (TAK-264, formerly MLN0264) comprising a fully human anti-GCC monoclonal antibody conjugated to monomethyl auristatin E via a protease-cleavable peptide linker. TAK-264 specifically bound, was internalized by, and killed GCC-expressing cells in vitro in an antigen-density-dependent manner. In GCC-expressing xenograft models with similar GCC expression levels/patterns observed in human mCRC samples, TAK-264 induced cell death, leading to tumor regressions and long-term tumor growth inhibition. TAK-264 antitumor activity was generally antigen-density-dependent, although some GCC-expressing tumors were refractory to TAK-264-targeted high local concentrations of payload. These data support further evaluation of TAK-264 in the treatment of GCC-expressing tumors.
doi_str_mv 10.1371/journal.pone.0191046
format Article
fullrecord <record><control><sourceid>proquest_plos_</sourceid><recordid>TN_cdi_plos_journals_2390639626</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_a7f83c04c46d4ef7a8377d00d5a34370</doaj_id><sourcerecordid>2390639626</sourcerecordid><originalsourceid>FETCH-LOGICAL-c526t-c28b32df6a5e2ddebfea1dca24879549b0203685814b81409b8562c67d2a82273</originalsourceid><addsrcrecordid>eNptkk1v1DAQhiMEoh_wDxBE4sIli7_i2BekalVKpUpc4GxNbCf1KmsvtrPq3vrT8Xa3VYs4WPbYz7yeGb1V9QGjBaYd_roKc_QwLTbB2wXCEiPGX1WnWFLScILo62fnk-ospRVCLRWcv61OiKQdwkKeVvcX9Tr4sLb5djfVMEeXMmTn68tGB7-aR8jW1OCz64PZ1TnU4wx-NxVY7_QEydbL2qUS5JDDndN7JEMcbW7s3SbalJwfa22nKdVFdutyDEXPHIJteFe9GWBK9v1xP69-f7_8tfzR3Py8ul5e3DS6JTw3moieEjNwaC0xxvaDBWw0ECY62TLZo9ImF63ArC8LyV60nGjeGQKCkI6eV58OupspJHUcXlKESsSp5IQX4vpAmAArtYluDXGnAjj1cBHiqCBmpyeroBsE1Yhpxg2zQweCdp1ByLRAWRlt0fp2_G3u19Zo63OE6YXoyxfvbtUYtqrtBJMPxXw5CsTwZ7Ypq7VL-ymCt2FOCktJEBItYwX9_A_6_-7YgdIxpBTt8FQMRmpvqMcstTeUOhqqpH183shT0qOD6F-L88sw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2390639626</pqid></control><display><type>article</type><title>A monomethyl auristatin E-conjugated antibody to guanylyl cyclase C is cytotoxic to target-expressing cells in vitro and in vivo</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Public Library of Science (PLoS)</source><creator>Gallery, Melissa ; Zhang, Julie ; Bradley, Daniel P ; Brauer, Pamela ; Cvet, Donna ; Estevam, Jose ; Danaee, Hadi ; Greenfield, Edward ; Li, Ping ; Manfredi, Mark ; Loke, Huay-Keng ; Rabino, Claudia ; Stringer, Brad ; Williamson, Mark ; Wyant, Tim ; Yang, Johnny ; Zhu, Qing ; Abu-Yousif, Adnan ; Veiby, O Petter</creator><creatorcontrib>Gallery, Melissa ; Zhang, Julie ; Bradley, Daniel P ; Brauer, Pamela ; Cvet, Donna ; Estevam, Jose ; Danaee, Hadi ; Greenfield, Edward ; Li, Ping ; Manfredi, Mark ; Loke, Huay-Keng ; Rabino, Claudia ; Stringer, Brad ; Williamson, Mark ; Wyant, Tim ; Yang, Johnny ; Zhu, Qing ; Abu-Yousif, Adnan ; Veiby, O Petter</creatorcontrib><description>Guanylyl cyclase C (GCC) is a cell-surface protein that is expressed by normal intestinal epithelial cells, more than 95% of metastatic colorectal cancers (mCRC), and the majority of gastric and pancreatic cancers. Due to strict apical localization, systemically delivered GCC-targeting agents should not reach GCC in normal intestinal tissue, while accessing antigen in tumor. We generated an investigational antibody-drug conjugate (TAK-264, formerly MLN0264) comprising a fully human anti-GCC monoclonal antibody conjugated to monomethyl auristatin E via a protease-cleavable peptide linker. TAK-264 specifically bound, was internalized by, and killed GCC-expressing cells in vitro in an antigen-density-dependent manner. In GCC-expressing xenograft models with similar GCC expression levels/patterns observed in human mCRC samples, TAK-264 induced cell death, leading to tumor regressions and long-term tumor growth inhibition. TAK-264 antitumor activity was generally antigen-density-dependent, although some GCC-expressing tumors were refractory to TAK-264-targeted high local concentrations of payload. These data support further evaluation of TAK-264 in the treatment of GCC-expressing tumors.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0191046</identifier><identifier>PMID: 29370189</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Anticancer properties ; Antigens ; Antitumor activity ; Biology ; Biology and Life Sciences ; Biomarkers ; Cancer ; Cell death ; Cell surface ; Colorectal cancer ; Cytotoxicity ; Density ; Epithelial cells ; Guanylate cyclase ; Immunoglobulins ; Intestine ; Ligands ; Localization ; Lymphoma ; Medical prognosis ; Medicine and Health Sciences ; Metastases ; Metastasis ; Monoclonal antibodies ; Oncology ; Pancreas ; Pancreatic cancer ; Pharmaceutical industry ; Pharmacology ; Proteins ; Research and Analysis Methods ; Tumors ; Xenografts ; Xenotransplantation</subject><ispartof>PloS one, 2018-01, Vol.13 (1), p.e0191046-e0191046</ispartof><rights>2018 Gallery et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 Gallery et al 2018 Gallery et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-c28b32df6a5e2ddebfea1dca24879549b0203685814b81409b8562c67d2a82273</citedby><cites>FETCH-LOGICAL-c526t-c28b32df6a5e2ddebfea1dca24879549b0203685814b81409b8562c67d2a82273</cites><orcidid>0000-0001-6230-813X</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/PMC5784926/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784926/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29370189$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gallery, Melissa</creatorcontrib><creatorcontrib>Zhang, Julie</creatorcontrib><creatorcontrib>Bradley, Daniel P</creatorcontrib><creatorcontrib>Brauer, Pamela</creatorcontrib><creatorcontrib>Cvet, Donna</creatorcontrib><creatorcontrib>Estevam, Jose</creatorcontrib><creatorcontrib>Danaee, Hadi</creatorcontrib><creatorcontrib>Greenfield, Edward</creatorcontrib><creatorcontrib>Li, Ping</creatorcontrib><creatorcontrib>Manfredi, Mark</creatorcontrib><creatorcontrib>Loke, Huay-Keng</creatorcontrib><creatorcontrib>Rabino, Claudia</creatorcontrib><creatorcontrib>Stringer, Brad</creatorcontrib><creatorcontrib>Williamson, Mark</creatorcontrib><creatorcontrib>Wyant, Tim</creatorcontrib><creatorcontrib>Yang, Johnny</creatorcontrib><creatorcontrib>Zhu, Qing</creatorcontrib><creatorcontrib>Abu-Yousif, Adnan</creatorcontrib><creatorcontrib>Veiby, O Petter</creatorcontrib><title>A monomethyl auristatin E-conjugated antibody to guanylyl cyclase C is cytotoxic to target-expressing cells in vitro and in vivo</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Guanylyl cyclase C (GCC) is a cell-surface protein that is expressed by normal intestinal epithelial cells, more than 95% of metastatic colorectal cancers (mCRC), and the majority of gastric and pancreatic cancers. Due to strict apical localization, systemically delivered GCC-targeting agents should not reach GCC in normal intestinal tissue, while accessing antigen in tumor. We generated an investigational antibody-drug conjugate (TAK-264, formerly MLN0264) comprising a fully human anti-GCC monoclonal antibody conjugated to monomethyl auristatin E via a protease-cleavable peptide linker. TAK-264 specifically bound, was internalized by, and killed GCC-expressing cells in vitro in an antigen-density-dependent manner. In GCC-expressing xenograft models with similar GCC expression levels/patterns observed in human mCRC samples, TAK-264 induced cell death, leading to tumor regressions and long-term tumor growth inhibition. TAK-264 antitumor activity was generally antigen-density-dependent, although some GCC-expressing tumors were refractory to TAK-264-targeted high local concentrations of payload. These data support further evaluation of TAK-264 in the treatment of GCC-expressing tumors.</description><subject>Anticancer properties</subject><subject>Antigens</subject><subject>Antitumor activity</subject><subject>Biology</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Cell death</subject><subject>Cell surface</subject><subject>Colorectal cancer</subject><subject>Cytotoxicity</subject><subject>Density</subject><subject>Epithelial cells</subject><subject>Guanylate cyclase</subject><subject>Immunoglobulins</subject><subject>Intestine</subject><subject>Ligands</subject><subject>Localization</subject><subject>Lymphoma</subject><subject>Medical prognosis</subject><subject>Medicine and Health Sciences</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Monoclonal antibodies</subject><subject>Oncology</subject><subject>Pancreas</subject><subject>Pancreatic cancer</subject><subject>Pharmaceutical industry</subject><subject>Pharmacology</subject><subject>Proteins</subject><subject>Research and Analysis Methods</subject><subject>Tumors</subject><subject>Xenografts</subject><subject>Xenotransplantation</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEoh_wDxBE4sIli7_i2BekalVKpUpc4GxNbCf1KmsvtrPq3vrT8Xa3VYs4WPbYz7yeGb1V9QGjBaYd_roKc_QwLTbB2wXCEiPGX1WnWFLScILo62fnk-ospRVCLRWcv61OiKQdwkKeVvcX9Tr4sLb5djfVMEeXMmTn68tGB7-aR8jW1OCz64PZ1TnU4wx-NxVY7_QEydbL2qUS5JDDndN7JEMcbW7s3SbalJwfa22nKdVFdutyDEXPHIJteFe9GWBK9v1xP69-f7_8tfzR3Py8ul5e3DS6JTw3moieEjNwaC0xxvaDBWw0ECY62TLZo9ImF63ArC8LyV60nGjeGQKCkI6eV58OupspJHUcXlKESsSp5IQX4vpAmAArtYluDXGnAjj1cBHiqCBmpyeroBsE1Yhpxg2zQweCdp1ByLRAWRlt0fp2_G3u19Zo63OE6YXoyxfvbtUYtqrtBJMPxXw5CsTwZ7Ypq7VL-ymCt2FOCktJEBItYwX9_A_6_-7YgdIxpBTt8FQMRmpvqMcstTeUOhqqpH183shT0qOD6F-L88sw</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Gallery, Melissa</creator><creator>Zhang, Julie</creator><creator>Bradley, Daniel P</creator><creator>Brauer, Pamela</creator><creator>Cvet, Donna</creator><creator>Estevam, Jose</creator><creator>Danaee, Hadi</creator><creator>Greenfield, Edward</creator><creator>Li, Ping</creator><creator>Manfredi, Mark</creator><creator>Loke, Huay-Keng</creator><creator>Rabino, Claudia</creator><creator>Stringer, Brad</creator><creator>Williamson, Mark</creator><creator>Wyant, Tim</creator><creator>Yang, Johnny</creator><creator>Zhu, Qing</creator><creator>Abu-Yousif, Adnan</creator><creator>Veiby, O Petter</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6230-813X</orcidid></search><sort><creationdate>20180101</creationdate><title>A monomethyl auristatin E-conjugated antibody to guanylyl cyclase C is cytotoxic to target-expressing cells in vitro and in vivo</title><author>Gallery, Melissa ; Zhang, Julie ; Bradley, Daniel P ; Brauer, Pamela ; Cvet, Donna ; Estevam, Jose ; Danaee, Hadi ; Greenfield, Edward ; Li, Ping ; Manfredi, Mark ; Loke, Huay-Keng ; Rabino, Claudia ; Stringer, Brad ; Williamson, Mark ; Wyant, Tim ; Yang, Johnny ; Zhu, Qing ; Abu-Yousif, Adnan ; Veiby, O Petter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-c28b32df6a5e2ddebfea1dca24879549b0203685814b81409b8562c67d2a82273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anticancer properties</topic><topic>Antigens</topic><topic>Antitumor activity</topic><topic>Biology</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Cancer</topic><topic>Cell death</topic><topic>Cell surface</topic><topic>Colorectal cancer</topic><topic>Cytotoxicity</topic><topic>Density</topic><topic>Epithelial cells</topic><topic>Guanylate cyclase</topic><topic>Immunoglobulins</topic><topic>Intestine</topic><topic>Ligands</topic><topic>Localization</topic><topic>Lymphoma</topic><topic>Medical prognosis</topic><topic>Medicine and Health Sciences</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Monoclonal antibodies</topic><topic>Oncology</topic><topic>Pancreas</topic><topic>Pancreatic cancer</topic><topic>Pharmaceutical industry</topic><topic>Pharmacology</topic><topic>Proteins</topic><topic>Research and Analysis Methods</topic><topic>Tumors</topic><topic>Xenografts</topic><topic>Xenotransplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gallery, Melissa</creatorcontrib><creatorcontrib>Zhang, Julie</creatorcontrib><creatorcontrib>Bradley, Daniel P</creatorcontrib><creatorcontrib>Brauer, Pamela</creatorcontrib><creatorcontrib>Cvet, Donna</creatorcontrib><creatorcontrib>Estevam, Jose</creatorcontrib><creatorcontrib>Danaee, Hadi</creatorcontrib><creatorcontrib>Greenfield, Edward</creatorcontrib><creatorcontrib>Li, Ping</creatorcontrib><creatorcontrib>Manfredi, Mark</creatorcontrib><creatorcontrib>Loke, Huay-Keng</creatorcontrib><creatorcontrib>Rabino, Claudia</creatorcontrib><creatorcontrib>Stringer, Brad</creatorcontrib><creatorcontrib>Williamson, Mark</creatorcontrib><creatorcontrib>Wyant, Tim</creatorcontrib><creatorcontrib>Yang, Johnny</creatorcontrib><creatorcontrib>Zhu, Qing</creatorcontrib><creatorcontrib>Abu-Yousif, Adnan</creatorcontrib><creatorcontrib>Veiby, O Petter</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallery, Melissa</au><au>Zhang, Julie</au><au>Bradley, Daniel P</au><au>Brauer, Pamela</au><au>Cvet, Donna</au><au>Estevam, Jose</au><au>Danaee, Hadi</au><au>Greenfield, Edward</au><au>Li, Ping</au><au>Manfredi, Mark</au><au>Loke, Huay-Keng</au><au>Rabino, Claudia</au><au>Stringer, Brad</au><au>Williamson, Mark</au><au>Wyant, Tim</au><au>Yang, Johnny</au><au>Zhu, Qing</au><au>Abu-Yousif, Adnan</au><au>Veiby, O Petter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A monomethyl auristatin E-conjugated antibody to guanylyl cyclase C is cytotoxic to target-expressing cells in vitro and in vivo</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>13</volume><issue>1</issue><spage>e0191046</spage><epage>e0191046</epage><pages>e0191046-e0191046</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Guanylyl cyclase C (GCC) is a cell-surface protein that is expressed by normal intestinal epithelial cells, more than 95% of metastatic colorectal cancers (mCRC), and the majority of gastric and pancreatic cancers. Due to strict apical localization, systemically delivered GCC-targeting agents should not reach GCC in normal intestinal tissue, while accessing antigen in tumor. We generated an investigational antibody-drug conjugate (TAK-264, formerly MLN0264) comprising a fully human anti-GCC monoclonal antibody conjugated to monomethyl auristatin E via a protease-cleavable peptide linker. TAK-264 specifically bound, was internalized by, and killed GCC-expressing cells in vitro in an antigen-density-dependent manner. In GCC-expressing xenograft models with similar GCC expression levels/patterns observed in human mCRC samples, TAK-264 induced cell death, leading to tumor regressions and long-term tumor growth inhibition. TAK-264 antitumor activity was generally antigen-density-dependent, although some GCC-expressing tumors were refractory to TAK-264-targeted high local concentrations of payload. These data support further evaluation of TAK-264 in the treatment of GCC-expressing tumors.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29370189</pmid><doi>10.1371/journal.pone.0191046</doi><orcidid>https://orcid.org/0000-0001-6230-813X</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2018-01, Vol.13 (1), p.e0191046-e0191046
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_2390639626
source DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS)
subjects Anticancer properties
Antigens
Antitumor activity
Biology
Biology and Life Sciences
Biomarkers
Cancer
Cell death
Cell surface
Colorectal cancer
Cytotoxicity
Density
Epithelial cells
Guanylate cyclase
Immunoglobulins
Intestine
Ligands
Localization
Lymphoma
Medical prognosis
Medicine and Health Sciences
Metastases
Metastasis
Monoclonal antibodies
Oncology
Pancreas
Pancreatic cancer
Pharmaceutical industry
Pharmacology
Proteins
Research and Analysis Methods
Tumors
Xenografts
Xenotransplantation
title A monomethyl auristatin E-conjugated antibody to guanylyl cyclase C is cytotoxic to target-expressing cells in vitro and in vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-20T16%3A23%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20monomethyl%20auristatin%20E-conjugated%20antibody%20to%20guanylyl%20cyclase%20C%20is%20cytotoxic%20to%20target-expressing%20cells%20in%20vitro%20and%20in%20vivo&rft.jtitle=PloS%20one&rft.au=Gallery,%20Melissa&rft.date=2018-01-01&rft.volume=13&rft.issue=1&rft.spage=e0191046&rft.epage=e0191046&rft.pages=e0191046-e0191046&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0191046&rft_dat=%3Cproquest_plos_%3E2390639626%3C/proquest_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2390639626&rft_id=info:pmid/29370189&rft_doaj_id=oai_doaj_org_article_a7f83c04c46d4ef7a8377d00d5a34370&rfr_iscdi=true