Please use this identifier to cite or link to this item:
https://doi.org/10.1038/s41598-018-30070-z
DC Field | Value | |
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dc.title | Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer | |
dc.contributor.author | Tan, H.L | |
dc.contributor.author | Yong, C | |
dc.contributor.author | Tan, B.Z | |
dc.contributor.author | Fong, W.J | |
dc.contributor.author | Padmanabhan, J | |
dc.contributor.author | Chin, A | |
dc.contributor.author | Ding, V | |
dc.contributor.author | Lau, A | |
dc.contributor.author | Zheng, L | |
dc.contributor.author | Bi, X | |
dc.contributor.author | Yang, Y | |
dc.contributor.author | Choo, A | |
dc.date.accessioned | 2020-10-20T03:25:38Z | |
dc.date.available | 2020-10-20T03:25:38Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Tan, H.L, Yong, C, Tan, B.Z, Fong, W.J, Padmanabhan, J, Chin, A, Ding, V, Lau, A, Zheng, L, Bi, X, Yang, Y, Choo, A (2018). Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer. Scientific Reports 8 (1) : 11608. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-30070-z | |
dc.identifier.issn | 20452322 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/177811 | |
dc.description.abstract | Monoclonal antibodies (mAbs) are used as targeted therapies against cancers. These mAbs kill cancer cells via various mechanisms of actions. In this study, human embryonic stem cells (hESCs) was used as the immunogen to generate a panel of antibodies. From this panel of mAbs, A19 was found to bind both hESC and various cancer cell lines. The antigen target of A19 was identified as Erbb-2 and glycan analysis showed that A19 binds to a N-glycan epitope on the antigen. A19 was elucidated to internalize into cancer cells following binding to Erbb-2 and hence developed as an antibody-drug conjugate (ADC). Using ADC as the mechanism of action, A19 was able to kill cancer cells in vitro and delayed the onset of tumour formation in mice xenograft model. When compared to Herceptin, A19 binds to different isoforms of Erbb-2 and does not compete with Herceptin for the same epitope. Hence, A19 has the potential to be developed as an alternative targeted therapeutic agent for cancers expressing Erbb-2. © 2018, The Author(s). | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | immunological antineoplastic agent | |
dc.subject | monoclonal antibody | |
dc.subject | oncofetal antigens | |
dc.subject | tumor antigen | |
dc.subject | animal | |
dc.subject | Bagg albino mouse | |
dc.subject | drug screening | |
dc.subject | experimental neoplasm | |
dc.subject | female | |
dc.subject | human | |
dc.subject | human embryonic stem cell | |
dc.subject | immunology | |
dc.subject | nude mouse | |
dc.subject | pathology | |
dc.subject | tumor cell line | |
dc.subject | Animals | |
dc.subject | Antibodies, Monoclonal, Murine-Derived | |
dc.subject | Antigens, Neoplasm | |
dc.subject | Antineoplastic Agents, Immunological | |
dc.subject | Cell Line, Tumor | |
dc.subject | Female | |
dc.subject | Human Embryonic Stem Cells | |
dc.subject | Humans | |
dc.subject | Mice, Inbred BALB C | |
dc.subject | Mice, Nude | |
dc.subject | Neoplasms, Experimental | |
dc.subject | Xenograft Model Antitumor Assays | |
dc.type | Article | |
dc.contributor.department | BIOMEDICAL ENGINEERING | |
dc.description.doi | 10.1038/s41598-018-30070-z | |
dc.description.sourcetitle | Scientific Reports | |
dc.description.volume | 8 | |
dc.description.issue | 1 | |
dc.description.page | 11608 | |
Appears in Collections: | Staff Publications Elements |
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