A chimeric antibody to L1 cell adhesion molecule shows therapeutic effect in an intrahepatic cholangiocarcinoma model

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dc.contributor.authorE S Lee-
dc.contributor.authorM S Jeong-
dc.contributor.authorR Singh-
dc.contributor.authorJuyeon Jung-
dc.contributor.authorHyunho Yoon-
dc.contributor.authorJeong Ki Min-
dc.contributor.authorK H Kim-
dc.contributor.authorH J Hong-
dc.date.accessioned2017-04-19T09:30:16Z-
dc.date.available2017-04-19T09:30:16Z-
dc.date.issued2012-
dc.identifier.issnI0000028-
dc.identifier.uri10.3858/emm.2012.44.4.027ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10723-
dc.description.abstractIntrahepatic cholangiocarcinoma (ICC), a malignant tumor derived from the intrahepatic bile duct epithelium, has a poor prognosis and is refractory to conventional chemotherapy and radiation therapy. Thus, there is an urgent need to develop new effective therapeutic strategies for this disease. We previously found that L1 cell adhesion molecule (L1CAM) plays an important role in tumor progression of ICC, and we generated a murine mAb, A10-A3 (IgG1), that binds to the Ig1 domain of L1CAM. In the present study, we further characterized A10-A3, constructed a chimeric A10-A3 antibody (cA10-A3) containing the constant regions of human IgG1, and evaluated the therapeutic potential in a human ICC xenograft nude mice model. The affinities (K D) of A10-A3 and cA10-A3 for soluble L1CAM were 1.8 nM and 1.9 nM, respectively, as determined by competition ELISA. A10-A3 inhibited L1CAM homo-philic binding and was slowly internalized into the tumor cells, but it did not significantly inhibit proliferation of ICC cells in vitro. cA10-A3 mediated antibody-dependent cell-mediated cytotoxicity in vitro and displayed anti-tumor activity in the ICC animal model. These results suggest that the humanized A10-A3 antibody may have potential as an anticancer agent for the treatment of ICC.-
dc.publisherSpringer-Nature Pub Group-
dc.titleA chimeric antibody to L1 cell adhesion molecule shows therapeutic effect in an intrahepatic cholangiocarcinoma model-
dc.title.alternativeA chimeric antibody to L1 cell adhesion molecule shows therapeutic effect in an intrahepatic cholangiocarcinoma model-
dc.typeArticle-
dc.citation.titleExperimental and Molecular Medicine-
dc.citation.number4-
dc.citation.endPage302-
dc.citation.startPage293-
dc.citation.volume44-
dc.contributor.affiliatedAuthorJuyeon Jung-
dc.contributor.affiliatedAuthorJeong Ki Min-
dc.contributor.alternativeName이응숙-
dc.contributor.alternativeName정문식-
dc.contributor.alternativeNameSingh-
dc.contributor.alternativeName정주연-
dc.contributor.alternativeName윤현호-
dc.contributor.alternativeName민정기-
dc.contributor.alternativeName김경현-
dc.contributor.alternativeName홍효정-
dc.identifier.bibliographicCitationExperimental and Molecular Medicine, vol. 44, no. 4, pp. 293-302-
dc.identifier.doi10.3858/emm.2012.44.4.027-
dc.subject.keywordImmunization-
dc.subject.keywordIntrahepatic chol-angiocarcinoma-
dc.subject.keywordNeural cell adhesion molecule L1-
dc.subject.keywordPassive-
dc.subject.localImmunization-
dc.subject.localIntrahepatic chol-angiocarcinoma-
dc.subject.localIntrahepatic cholangiocarcinoma-
dc.subject.localNeural cell adhesion molecule L1-
dc.subject.localPassive-
dc.description.journalClassY-
Appears in Collections:
Division of Biomaterials Research > Bionanotechnology Research Center > 1. Journal Articles
Division of Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
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