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A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo
To create a new anti-tumor antibody, we conducted signal sequence trap by retrovirus-meditated expression method and identified coxsackie virus and adenovirus receptor (CXADR) as an appropriate target. We developed monoclonal antibodies against human CXADR and found that one antibody (6G10A) signifi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225458/ https://www.ncbi.nlm.nih.gov/pubmed/28074864 http://dx.doi.org/10.1038/srep40400 |
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author | Kawada, Manabu Inoue, Hiroyuki Kajikawa, Masunori Sugiura, Masahito Sakamoto, Shuichi Urano, Sakiko Karasawa, Chigusa Usami, Ihomi Futakuchi, Mitsuru Masuda, Tohru |
author_facet | Kawada, Manabu Inoue, Hiroyuki Kajikawa, Masunori Sugiura, Masahito Sakamoto, Shuichi Urano, Sakiko Karasawa, Chigusa Usami, Ihomi Futakuchi, Mitsuru Masuda, Tohru |
author_sort | Kawada, Manabu |
collection | PubMed |
description | To create a new anti-tumor antibody, we conducted signal sequence trap by retrovirus-meditated expression method and identified coxsackie virus and adenovirus receptor (CXADR) as an appropriate target. We developed monoclonal antibodies against human CXADR and found that one antibody (6G10A) significantly inhibited the growth of subcutaneous as well as orthotopic xenografts of human prostate cancer cells in vivo. Furthermore, 6G10A also inhibited other cancer xenografts expressing CXADR, such as pancreatic and colorectal cancer cells. Knockdown and overexpression of CXADR confirmed the dependence of its anti-tumor activity on CXADR expression. Our studies of its action demonstrated that 6G10A exerted its anti-tumor activity primarily through both antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity. Moreover, 6G10A reacted with human tumor tissues, such as prostate, lung, and brain, each of which express CXADR. Although we need further evaluation of its reactivity and safety in human tissues, our results show that a novel anti-CXADR antibody may be a feasible candidate for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-5225458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52254582017-01-17 A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo Kawada, Manabu Inoue, Hiroyuki Kajikawa, Masunori Sugiura, Masahito Sakamoto, Shuichi Urano, Sakiko Karasawa, Chigusa Usami, Ihomi Futakuchi, Mitsuru Masuda, Tohru Sci Rep Article To create a new anti-tumor antibody, we conducted signal sequence trap by retrovirus-meditated expression method and identified coxsackie virus and adenovirus receptor (CXADR) as an appropriate target. We developed monoclonal antibodies against human CXADR and found that one antibody (6G10A) significantly inhibited the growth of subcutaneous as well as orthotopic xenografts of human prostate cancer cells in vivo. Furthermore, 6G10A also inhibited other cancer xenografts expressing CXADR, such as pancreatic and colorectal cancer cells. Knockdown and overexpression of CXADR confirmed the dependence of its anti-tumor activity on CXADR expression. Our studies of its action demonstrated that 6G10A exerted its anti-tumor activity primarily through both antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity. Moreover, 6G10A reacted with human tumor tissues, such as prostate, lung, and brain, each of which express CXADR. Although we need further evaluation of its reactivity and safety in human tissues, our results show that a novel anti-CXADR antibody may be a feasible candidate for cancer immunotherapy. Nature Publishing Group 2017-01-11 /pmc/articles/PMC5225458/ /pubmed/28074864 http://dx.doi.org/10.1038/srep40400 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kawada, Manabu Inoue, Hiroyuki Kajikawa, Masunori Sugiura, Masahito Sakamoto, Shuichi Urano, Sakiko Karasawa, Chigusa Usami, Ihomi Futakuchi, Mitsuru Masuda, Tohru A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
title | A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
title_full | A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
title_fullStr | A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
title_full_unstemmed | A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
title_short | A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
title_sort | novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225458/ https://www.ncbi.nlm.nih.gov/pubmed/28074864 http://dx.doi.org/10.1038/srep40400 |
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