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Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody
Photoimmunotherapy (PIT) is a new type of tumor‐specific treatment utilizing monoclonal antibody (mAb)‐photosensitizer conjugates and near‐infrared (NIR) light irradiation. One potential PIT target, the type I transmembrane protein TROP2, is expressed at high levels in many cancers, including pancre...
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/PMC6912056/ https://www.ncbi.nlm.nih.gov/pubmed/31674732 http://dx.doi.org/10.1002/cam4.2658 |
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author | Nishimura, Takashi Mitsunaga, Makoto Sawada, Ryoichi Saruta, Masayuki Kobayashi, Hisataka Matsumoto, Noriko Kanke, Toru Yanai, Hiroyuki Nakamura, Koji |
author_facet | Nishimura, Takashi Mitsunaga, Makoto Sawada, Ryoichi Saruta, Masayuki Kobayashi, Hisataka Matsumoto, Noriko Kanke, Toru Yanai, Hiroyuki Nakamura, Koji |
author_sort | Nishimura, Takashi |
collection | PubMed |
description | Photoimmunotherapy (PIT) is a new type of tumor‐specific treatment utilizing monoclonal antibody (mAb)‐photosensitizer conjugates and near‐infrared (NIR) light irradiation. One potential PIT target, the type I transmembrane protein TROP2, is expressed at high levels in many cancers, including pancreatic carcinoma (PC) and cholangiocarcinoma (CC), in which its expression is correlated with poor prognosis and tumor aggressiveness. In this study, we assessed the efficacy of PIT utilizing newly developed humanized anti‐TROP2 mAb conjugated to the photosensitizer IR700 (TROP2‐IR700) for PC and CC. Immunohistochemistry on PC and CC tissue microarrays confirmed that TROP2 is overexpressed in about half of PC and CC specimens. Using cultured PC and CC cells, TROP2‐IR700 localized TROP2‐specific and target‐specific cell killing was observed after NIR light irradiation. In addition, TROP2‐IR700 was localized to mouse xenograft tumors expressing TROP2 after intravenous injection. PC and CC xenograft tumor growth was significantly inhibited by TROP2‐targeted PIT relative to controls. The efficacy of TROP2‐targeted PIT in vitro and against xenografted tumors in vivo suggests promise as a therapy for human PC and CC, both of which currently have dismal prognoses and limited therapeutic options. |
format | Online Article Text |
id | pubmed-6912056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69120562019-12-23 Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody Nishimura, Takashi Mitsunaga, Makoto Sawada, Ryoichi Saruta, Masayuki Kobayashi, Hisataka Matsumoto, Noriko Kanke, Toru Yanai, Hiroyuki Nakamura, Koji Cancer Med Cancer Biology Photoimmunotherapy (PIT) is a new type of tumor‐specific treatment utilizing monoclonal antibody (mAb)‐photosensitizer conjugates and near‐infrared (NIR) light irradiation. One potential PIT target, the type I transmembrane protein TROP2, is expressed at high levels in many cancers, including pancreatic carcinoma (PC) and cholangiocarcinoma (CC), in which its expression is correlated with poor prognosis and tumor aggressiveness. In this study, we assessed the efficacy of PIT utilizing newly developed humanized anti‐TROP2 mAb conjugated to the photosensitizer IR700 (TROP2‐IR700) for PC and CC. Immunohistochemistry on PC and CC tissue microarrays confirmed that TROP2 is overexpressed in about half of PC and CC specimens. Using cultured PC and CC cells, TROP2‐IR700 localized TROP2‐specific and target‐specific cell killing was observed after NIR light irradiation. In addition, TROP2‐IR700 was localized to mouse xenograft tumors expressing TROP2 after intravenous injection. PC and CC xenograft tumor growth was significantly inhibited by TROP2‐targeted PIT relative to controls. The efficacy of TROP2‐targeted PIT in vitro and against xenografted tumors in vivo suggests promise as a therapy for human PC and CC, both of which currently have dismal prognoses and limited therapeutic options. John Wiley and Sons Inc. 2019-11-01 /pmc/articles/PMC6912056/ /pubmed/31674732 http://dx.doi.org/10.1002/cam4.2658 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Biology Nishimura, Takashi Mitsunaga, Makoto Sawada, Ryoichi Saruta, Masayuki Kobayashi, Hisataka Matsumoto, Noriko Kanke, Toru Yanai, Hiroyuki Nakamura, Koji Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody |
title | Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody |
title_full | Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody |
title_fullStr | Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody |
title_full_unstemmed | Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody |
title_short | Photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐TROP2 antibody |
title_sort | photoimmunotherapy targeting biliary‐pancreatic cancer with humanized anti‐trop2 antibody |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912056/ https://www.ncbi.nlm.nih.gov/pubmed/31674732 http://dx.doi.org/10.1002/cam4.2658 |
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