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Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers
BACKGROUND: Nectin-2 is a Ca(2+)-independent cell-cell adhesion molecule that is one of the plasma membrane components of adherens junctions. However, little has been reported about the involvement of Nectin-2 in cancer. METHODS: To determine the expression of Nectin-2 in cancer tissues and cancer c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698035/ https://www.ncbi.nlm.nih.gov/pubmed/23758976 http://dx.doi.org/10.1186/1476-4598-12-60 |
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author | Oshima, Tsutomu Sato, Shuji Kato, Junichi Ito, Yuki Watanabe, Takahiro Tsuji, Isamu Hori, Akira Kurokawa, Tomofumi Kokubo, Toshio |
author_facet | Oshima, Tsutomu Sato, Shuji Kato, Junichi Ito, Yuki Watanabe, Takahiro Tsuji, Isamu Hori, Akira Kurokawa, Tomofumi Kokubo, Toshio |
author_sort | Oshima, Tsutomu |
collection | PubMed |
description | BACKGROUND: Nectin-2 is a Ca(2+)-independent cell-cell adhesion molecule that is one of the plasma membrane components of adherens junctions. However, little has been reported about the involvement of Nectin-2 in cancer. METHODS: To determine the expression of Nectin-2 in cancer tissues and cancer cell lines, we performed gene expression profile analysis, immunohistochemistry studies, and flow cytometry analysis. We also investigated the potential of this molecule as a target for antibody therapeutics to treat cancers by generating and characterizing an anti-Nectin-2 rabbit polyclonal antibody (poAb) and 256 fully human anti-Nectin-2 monoclonal antibodies (mAbs). In addition, we tested anti-Nectin-2 mAbs in several in vivo tumor growth inhibition models to investigate the primary mechanisms of action of the mAbs. RESULTS: In the present study, we found that Nectin-2 was over-expressed in clinical breast and ovarian cancer tissues by using gene expression profile analysis and immunohistochemistry studies. Nectin-2 was over-expressed in various cancer cell lines as well. Furthermore, the polyclonal antibody specific to Nectin-2 suppressed the in vitro proliferation of OV-90 ovarian cancer cells, which express endogenous Nectin-2 on the cell surface. The anti-Nectin-2 mAbs we generated were classified into 7 epitope bins. The anti-Nectin-2 mAbs demonstrated antibody-dependent cellular cytotoxicity (ADCC) and epitope bin-dependent features such as the inhibition of Nectin-2-Nectin-2 interaction, Nectin-2-Nectin-3 interaction, and in vitro cancer cell proliferation. A representative anti-Nectin-2 mAb in epitope bin VII, Y-443, showed anti-tumor effects against OV-90 cells and MDA-MB-231 breast cancer cells in mouse therapeutic models, and its main mechanism of action appeared to be ADCC. CONCLUSIONS: We observed the over-expression of Nectin-2 in breast and ovarian cancers and anti-tumor activity of anti-Nectin-2 mAbs via strong ADCC. These findings suggest that Nectin-2 is a potential target for antibody therapy against breast and ovarian cancers. |
format | Online Article Text |
id | pubmed-3698035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36980352013-07-02 Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers Oshima, Tsutomu Sato, Shuji Kato, Junichi Ito, Yuki Watanabe, Takahiro Tsuji, Isamu Hori, Akira Kurokawa, Tomofumi Kokubo, Toshio Mol Cancer Research BACKGROUND: Nectin-2 is a Ca(2+)-independent cell-cell adhesion molecule that is one of the plasma membrane components of adherens junctions. However, little has been reported about the involvement of Nectin-2 in cancer. METHODS: To determine the expression of Nectin-2 in cancer tissues and cancer cell lines, we performed gene expression profile analysis, immunohistochemistry studies, and flow cytometry analysis. We also investigated the potential of this molecule as a target for antibody therapeutics to treat cancers by generating and characterizing an anti-Nectin-2 rabbit polyclonal antibody (poAb) and 256 fully human anti-Nectin-2 monoclonal antibodies (mAbs). In addition, we tested anti-Nectin-2 mAbs in several in vivo tumor growth inhibition models to investigate the primary mechanisms of action of the mAbs. RESULTS: In the present study, we found that Nectin-2 was over-expressed in clinical breast and ovarian cancer tissues by using gene expression profile analysis and immunohistochemistry studies. Nectin-2 was over-expressed in various cancer cell lines as well. Furthermore, the polyclonal antibody specific to Nectin-2 suppressed the in vitro proliferation of OV-90 ovarian cancer cells, which express endogenous Nectin-2 on the cell surface. The anti-Nectin-2 mAbs we generated were classified into 7 epitope bins. The anti-Nectin-2 mAbs demonstrated antibody-dependent cellular cytotoxicity (ADCC) and epitope bin-dependent features such as the inhibition of Nectin-2-Nectin-2 interaction, Nectin-2-Nectin-3 interaction, and in vitro cancer cell proliferation. A representative anti-Nectin-2 mAb in epitope bin VII, Y-443, showed anti-tumor effects against OV-90 cells and MDA-MB-231 breast cancer cells in mouse therapeutic models, and its main mechanism of action appeared to be ADCC. CONCLUSIONS: We observed the over-expression of Nectin-2 in breast and ovarian cancers and anti-tumor activity of anti-Nectin-2 mAbs via strong ADCC. These findings suggest that Nectin-2 is a potential target for antibody therapy against breast and ovarian cancers. BioMed Central 2013-06-12 /pmc/articles/PMC3698035/ /pubmed/23758976 http://dx.doi.org/10.1186/1476-4598-12-60 Text en Copyright © 2013 Oshima et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Oshima, Tsutomu Sato, Shuji Kato, Junichi Ito, Yuki Watanabe, Takahiro Tsuji, Isamu Hori, Akira Kurokawa, Tomofumi Kokubo, Toshio Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
title | Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
title_full | Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
title_fullStr | Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
title_full_unstemmed | Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
title_short | Nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
title_sort | nectin-2 is a potential target for antibody therapy of breast and ovarian cancers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698035/ https://www.ncbi.nlm.nih.gov/pubmed/23758976 http://dx.doi.org/10.1186/1476-4598-12-60 |
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