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dc.contributor.author문병석*
dc.date.accessioned2019-10-29T16:30:28Z-
dc.date.available2019-10-29T16:30:28Z-
dc.date.issued2019*
dc.identifier.issn1078-0432*
dc.identifier.otherOAK-25543*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/251652-
dc.description.abstractPurpose: Cholangiocarcinoma is a malignancy of bile duct with a poor prognosis. Conventional chemotherapy and radiotherapy are generally ineffective, and surgical resection is the only curative treatment for cholangiocarcinoma. L1-cell adhesion molecule (L1CAM) has been known as a novel prognostic marker and therapeutic target for cholangiocarcinoma. This study aimed to evaluate the feasibility of immuno-PET imaging–based radioimmunotherapy using radiolabeled anti-L1CAM antibody in cholangiocarcinoma xenograft model. Experimental Design: We prepared a theranostic convergence bioradiopharmaceutical using chimeric anti-L1CAM antibody (cA10-A3) conjugated with 1,4,7-triazacyclono-nane-1,4,7-triacetic acid (NOTA) chelator and labeled with 64Cu or 177Lu and evaluated the immuno-PET or SPECT/CT imaging and biodistribution with 64Cu-/177Lu-cA10-A3 in various cholangiocarcinoma xenograft models. Therapeutic efficacy and response monitoring were performed by 177Lu-cA10-A3 and 18F-FDG-PET, respectively, and immunohistochemistry was done by TUNEL and Ki-67. Results: Radiolabeled cA10-A3 antibodies specifically recognized L1CAM in vitro, clearly visualized cholangiocarcinoma tumors in immuno-PET and SPECT/CT imaging, and differentiated the L1CAM expression level in cholangiocarcinoma xenograft models. 177Lu-cA10-A3 (12.95 MBq/100 mg) showed statistically significant reduction in tumor volumes (P < 0.05) and decreased glucose metabolism (P < 0.01). IHC analysis revealed 177Lu-cA10-A3 treatment increased TUNEL-positive and decreased Ki-67-positive cells, compared with saline, cA10-A3, or 177Lu-isotype. Conclusions: Anti-L1CAM immuno-PET imaging using 64Cu-cA10-A3 could be translated into the clinic for characterizing the pharmacokinetics and selecting appropriate patients for radioimmunotherapy. Radioimmunotherapy using 177Lu-cA10-A3 may provide survival benefit in L1CAM-expressing cholangiocarcinoma tumor. Theranostic convergence bioradiopharmaceutical strategy would be applied as imaging biomarker-based personalized medicine in L1CAM-expressing patients with cholangiocarcinoma. © 2019 American Association for Cancer Research.*
dc.languageEnglish*
dc.publisherAmerican Association for Cancer Research Inc.*
dc.titleDevelopment of a theranostic convergence bioradiopharmaceutical for immuno-PET based radioimmunotherapy of L1CAM in cholangiocarcinoma model*
dc.typeArticle*
dc.relation.issue20*
dc.relation.volume25*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage6148*
dc.relation.lastpage6159*
dc.relation.journaltitleClinical Cancer Research*
dc.identifier.doi10.1158/1078-0432.CCR-19-1157*
dc.identifier.wosidWOS:000494361900017*
dc.identifier.scopusid2-s2.0-85073309040*
dc.author.googleSong I.H.*
dc.author.googleJeong M.S.*
dc.author.googleHong H.J.*
dc.author.googleShin J.I.*
dc.author.googlePark Y.S.*
dc.author.googleWoo S.-K.*
dc.author.googleMoon B.S.*
dc.author.googleKim K.I.*
dc.author.googleLee Y.J.*
dc.author.googleKang J.H.*
dc.author.googleLee T.S.*
dc.contributor.scopusid문병석(22950995100;57206502981)*
dc.date.modifydate20240318142826*
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