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Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule
The present state of therapy for colorectal cancer (CRC) is far from satisfactory, highlighting the need for new targets for this disease. We identified a new CRC‐specific molecule, TMEM180, a predicted 11‐pass transmembrane protein that apparently functions as a cation symporter. We developed an an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361608/ https://www.ncbi.nlm.nih.gov/pubmed/30537002 http://dx.doi.org/10.1111/cas.13907 |
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author | Yasunaga, Masahiro Saijou, Shinji Hanaoka, Shingo Anzai, Takahiro Tsumura, Ryo Matsumura, Yasuhiro |
author_facet | Yasunaga, Masahiro Saijou, Shinji Hanaoka, Shingo Anzai, Takahiro Tsumura, Ryo Matsumura, Yasuhiro |
author_sort | Yasunaga, Masahiro |
collection | PubMed |
description | The present state of therapy for colorectal cancer (CRC) is far from satisfactory, highlighting the need for new targets for this disease. We identified a new CRC‐specific molecule, TMEM180, a predicted 11‐pass transmembrane protein that apparently functions as a cation symporter. We developed an anti‐TMEM180 mAb and then succeeded in humanizing the mAb. Immunohistochemistry (IHC) in CRC with the mAb showed a similar positivity rate as compared with anti‐epidermal growth factor receptor mAb, and IHC with anti‐TMEM180 mAb did not show staining in major organs used in this study. Immune electron microscopy clearly indicated that TMEM180 was present on the tumor exosome. The TMEM180 promoter region contains 10 hypoxia‐responsive element consensus sequences; accordingly, SW480 cells upregulated TMEM180 under low‐oxygen conditions. Anti‐TMEM180 mAb has in vitro antibody‐dependent cell‐mediated cytotoxicity and complement‐dependent cytotoxicity activity, and SW480 CRC xenografts were eradicated by the mAb. These data indicate that TMEM180 may be a new CRC marker and that a mAb against this protein could be used as antibody‐based therapy against CRC. |
format | Online Article Text |
id | pubmed-6361608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63616082019-02-14 Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule Yasunaga, Masahiro Saijou, Shinji Hanaoka, Shingo Anzai, Takahiro Tsumura, Ryo Matsumura, Yasuhiro Cancer Sci Original Articles The present state of therapy for colorectal cancer (CRC) is far from satisfactory, highlighting the need for new targets for this disease. We identified a new CRC‐specific molecule, TMEM180, a predicted 11‐pass transmembrane protein that apparently functions as a cation symporter. We developed an anti‐TMEM180 mAb and then succeeded in humanizing the mAb. Immunohistochemistry (IHC) in CRC with the mAb showed a similar positivity rate as compared with anti‐epidermal growth factor receptor mAb, and IHC with anti‐TMEM180 mAb did not show staining in major organs used in this study. Immune electron microscopy clearly indicated that TMEM180 was present on the tumor exosome. The TMEM180 promoter region contains 10 hypoxia‐responsive element consensus sequences; accordingly, SW480 cells upregulated TMEM180 under low‐oxygen conditions. Anti‐TMEM180 mAb has in vitro antibody‐dependent cell‐mediated cytotoxicity and complement‐dependent cytotoxicity activity, and SW480 CRC xenografts were eradicated by the mAb. These data indicate that TMEM180 may be a new CRC marker and that a mAb against this protein could be used as antibody‐based therapy against CRC. John Wiley and Sons Inc. 2019-01-04 2019-02 /pmc/articles/PMC6361608/ /pubmed/30537002 http://dx.doi.org/10.1111/cas.13907 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Yasunaga, Masahiro Saijou, Shinji Hanaoka, Shingo Anzai, Takahiro Tsumura, Ryo Matsumura, Yasuhiro Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule |
title | Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule |
title_full | Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule |
title_fullStr | Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule |
title_full_unstemmed | Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule |
title_short | Significant antitumor effect of an antibody against TMEM180, a new colorectal cancer‐specific molecule |
title_sort | significant antitumor effect of an antibody against tmem180, a new colorectal cancer‐specific molecule |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361608/ https://www.ncbi.nlm.nih.gov/pubmed/30537002 http://dx.doi.org/10.1111/cas.13907 |
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