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Development of a radionuclide-labeled monoclonal anti-CD55 antibody with theranostic potential in pleural metastatic lung cancer

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dc.contributor.author김락균-
dc.date.accessioned2018-08-28T17:25:34Z-
dc.date.available2018-08-28T17:25:34Z-
dc.date.issued2018-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/162589-
dc.description.abstractDecay-accelerating factor (CD55 or DAF) inhibits complement-dependent cytotoxicity. We determined that CD55 is overexpressed in 76.47% of human non-small cell lung cancer tissue specimens. We therefore developed a lutetium-177-labeled chimeric monoclonal antibody against CD55. CD55-specific single-chain variable fragment (scFv) was selected from a naive chicken scFv phage-display library, converted to IgG, and radiolabeled with lutetium-177 to generate a (177)Lu-anti-CD55 antibody. We then charaterized the biodistribution of this antibody in a mouse model of pleural metastatic lung cancer. The (177)Lu-anti-CD55 antibody was primarily retained in tumor tissue rather than normal tissue. Treatment of the mice with (177)Lu-anti-CD55 reduced the growth of lung tumors and improved median survival in vivo by two-fold compared to controls. Finally, (177)Lu-anti-CD55 also enhanced the antitumor activity of cisplatin both in vitro and in vivo. These data suggest (177)Lu-anti-CD55 antibody is a promising theranostic agent for pleural metastatic lung cancer.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleDevelopment of a radionuclide-labeled monoclonal anti-CD55 antibody with theranostic potential in pleural metastatic lung cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Life Science-
dc.contributor.googleauthorSo Hee Dho-
dc.contributor.googleauthorSoo Yong Kim-
dc.contributor.googleauthorChaeuk Chung-
dc.contributor.googleauthorEun Ha Cho-
dc.contributor.googleauthorSo-Young Lee-
dc.contributor.googleauthorJi Young Kim-
dc.contributor.googleauthorLark Kyun Kim-
dc.contributor.googleauthorSung-Won Min-
dc.contributor.googleauthorJichul Lee-
dc.contributor.googleauthorSung Hee Jung-
dc.contributor.googleauthorJae Cheong Lim-
dc.identifier.doi10.1038/s41598-018-27355-8-
dc.contributor.localIdA04520-
dc.relation.journalcodeJ02646-
dc.identifier.eissn2045-2322-
dc.identifier.pmid29895866-
dc.contributor.alternativeNameKim, Lark Kyun-
dc.contributor.affiliatedAuthorKim, Lark Kyun-
dc.citation.volume8-
dc.citation.number1-
dc.citation.startPage8960-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, Vol.8(1) : 8960, 2018-
dc.identifier.rimsid60169-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers

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