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dc.contributor.authorCheng, Tsai-Muen_US
dc.contributor.authorMurad, Yanal M.en_US
dc.contributor.authorChang, Chia-Chingen_US
dc.contributor.authorYang, Ming-Chien_US
dc.contributor.authorBaral, Toya Nathen_US
dc.contributor.authorCowan, Aaronen_US
dc.contributor.authorTseng, Shin-Huaen_US
dc.contributor.authorWong, Andrewen_US
dc.contributor.authorMacKenzie, Rogeren_US
dc.contributor.authorShieh, Dar-Binen_US
dc.contributor.authorZhang, Jianbingen_US
dc.date.accessioned2014-12-08T15:34:56Z-
dc.date.available2014-12-08T15:34:56Z-
dc.date.issued2014-03-01en_US
dc.identifier.issn0959-8049en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ejca.2012.07.019en_US
dc.identifier.urihttp://hdl.handle.net/11536/23756-
dc.description.abstractCarcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) is over-expressed in pancreatic cancer cells, and it is associated with the progression of pancreatic cancer. We tested a single domain antibody (sdAb) targeting CEACAM6, 2A3, which was isolated previously from a llama immune library, and an Fc conjugated version of this sdAb, to determine how they affect the pancreatic cancer cell line BxPC3. We also compared the effects of the antibodies to gemcitabine. Gemcitabine and 2A3 slowed down cancer cell proliferation. However, only 2A3 retarded cancer cell invasion, angiogenesis within the cancer mass and BxPC3 cell MMP-9 activity, three features important for tumour growth and metas- tasis. The IC(50)s for 2A3, 2A3-Fc and gemcitabine were determined as 6.5 mu M, 8 mu M and 12 nM, respectively. While the 2A3 antibody inhibited MMP-9 activity by 33% compared to non-treated control cells, gemcitabine failed to inhibit MMP-9 activity. Moreover, 2A3 and 2A3-Fc inhibited invasion of BxPC3 by 73% compared to non-treated cells. When conditioned media that were produced using 2A3- or 2A3-Fc-treated BxPC3 cells were used in a capillary formation assay, the capillary length was reduced by 21% and 49%, respectively. Therefore 2A3 is an ideal candidate for treating tumours that over-express CEACAM6. (C) 2012 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectCEACAM6en_US
dc.subjectSingle domain antibodiesen_US
dc.subjectPancreatic canceren_US
dc.subjectGemcitabineen_US
dc.subjectAngiogenesisen_US
dc.subjectMMP-9en_US
dc.subjectBxPC3en_US
dc.titleSingle domain antibody against carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) inhibits proliferation, migration, invasion and angiogenesis of pancreatic cancer cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ejca.2012.07.019en_US
dc.identifier.journalEUROPEAN JOURNAL OF CANCERen_US
dc.citation.volume50en_US
dc.citation.issue4en_US
dc.citation.spage713en_US
dc.citation.epage721en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000331715300005-
dc.citation.woscount0-
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