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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...

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Autores principales: Yasunaga, Masahiro, Saijou, Shinji, Hanaoka, Shingo, Anzai, Takahiro, Tsumura, Ryo, Matsumura, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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