Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-30070-z
Title: Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer
Authors: 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 
Keywords: immunological antineoplastic agent
monoclonal antibody
oncofetal antigens
tumor antigen
animal
Bagg albino mouse
drug screening
experimental neoplasm
female
human
human embryonic stem cell
immunology
nude mouse
pathology
tumor cell line
Animals
Antibodies, Monoclonal, Murine-Derived
Antigens, Neoplasm
Antineoplastic Agents, Immunological
Cell Line, Tumor
Female
Human Embryonic Stem Cells
Humans
Mice, Inbred BALB C
Mice, Nude
Neoplasms, Experimental
Xenograft Model Antitumor Assays
Issue Date: 2018
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
Rights: Attribution 4.0 International
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).
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/177811
ISSN: 20452322
DOI: 10.1038/s41598-018-30070-z
Rights: Attribution 4.0 International
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