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Near‐infrared photoimmunotherapy through bone

Near‐infrared photoimmunotherapy (NIR‐PIT) is a molecularly targeted cancer phototherapy that is based on injecting a conjugate of a silicon‐phthalocyanine derivative, IRdye 700DX (IR700), and a monoclonal antibody that targets an expressed antigen on the cancer cell surface. Subsequent local exposu...

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Autores principales: Nakamura, Yu A., Okuyama, Shuhei, Furusawa, Aki, Nagaya, Tadanobu, Fujimura, Daiki, Okada, Ryuhei, Maruoka, Yasuhiro, Eclarinal, Philip C., Choyke, Peter L., Kobayashi, Hisataka
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/PMC6890452/
https://www.ncbi.nlm.nih.gov/pubmed/31553485
http://dx.doi.org/10.1111/cas.14203
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author Nakamura, Yu A.
Okuyama, Shuhei
Furusawa, Aki
Nagaya, Tadanobu
Fujimura, Daiki
Okada, Ryuhei
Maruoka, Yasuhiro
Eclarinal, Philip C.
Choyke, Peter L.
Kobayashi, Hisataka
author_facet Nakamura, Yu A.
Okuyama, Shuhei
Furusawa, Aki
Nagaya, Tadanobu
Fujimura, Daiki
Okada, Ryuhei
Maruoka, Yasuhiro
Eclarinal, Philip C.
Choyke, Peter L.
Kobayashi, Hisataka
author_sort Nakamura, Yu A.
collection PubMed
description Near‐infrared photoimmunotherapy (NIR‐PIT) is a molecularly targeted cancer phototherapy that is based on injecting a conjugate of a silicon‐phthalocyanine derivative, IRdye 700DX (IR700), and a monoclonal antibody that targets an expressed antigen on the cancer cell surface. Subsequent local exposure to NIR light results in the rapid and highly selective immunogenic cell death of targeted cancer cells. Because many cancers grow in bones through which light does not penetrate well, the goal of this study was to determine if NIR‐PIT can effectively treat cancers in bone. A bovine rib was used as a bone sample. Because the sample’s NIR light transmittance was shown to be approximately 4.52% in preliminary tests, it was hypothesized that a maximum radiation dosage of 128 and 1500 J/cm(2) would be sufficient to induce cell death in in vitro target cells and in vivo mouse tumor models, respectively. Cell viability was measured through bioluminescence studies comparing relative luciferase activity, as well as a cytotoxicity assay. In the in vitro model, tumor cell viability was significantly decreased after 64 and 128 J/cm(2) NIR light irradiation through the bone. An in vivo mouse tumor model also showed that 1500 J/cm(2) NIR light irradiation through the bone significantly reduced tumor viability at both 24 and 48 hours posttreatment compared to the control group (P = .026 and .040 respectively). Therefore, despite limitations in light transmission, NIR‐PIT nevertheless is capable of effectively treating cancers within bone.
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spelling pubmed-68904522019-12-12 Near‐infrared photoimmunotherapy through bone Nakamura, Yu A. Okuyama, Shuhei Furusawa, Aki Nagaya, Tadanobu Fujimura, Daiki Okada, Ryuhei Maruoka, Yasuhiro Eclarinal, Philip C. Choyke, Peter L. Kobayashi, Hisataka Cancer Sci Original Articles Near‐infrared photoimmunotherapy (NIR‐PIT) is a molecularly targeted cancer phototherapy that is based on injecting a conjugate of a silicon‐phthalocyanine derivative, IRdye 700DX (IR700), and a monoclonal antibody that targets an expressed antigen on the cancer cell surface. Subsequent local exposure to NIR light results in the rapid and highly selective immunogenic cell death of targeted cancer cells. Because many cancers grow in bones through which light does not penetrate well, the goal of this study was to determine if NIR‐PIT can effectively treat cancers in bone. A bovine rib was used as a bone sample. Because the sample’s NIR light transmittance was shown to be approximately 4.52% in preliminary tests, it was hypothesized that a maximum radiation dosage of 128 and 1500 J/cm(2) would be sufficient to induce cell death in in vitro target cells and in vivo mouse tumor models, respectively. Cell viability was measured through bioluminescence studies comparing relative luciferase activity, as well as a cytotoxicity assay. In the in vitro model, tumor cell viability was significantly decreased after 64 and 128 J/cm(2) NIR light irradiation through the bone. An in vivo mouse tumor model also showed that 1500 J/cm(2) NIR light irradiation through the bone significantly reduced tumor viability at both 24 and 48 hours posttreatment compared to the control group (P = .026 and .040 respectively). Therefore, despite limitations in light transmission, NIR‐PIT nevertheless is capable of effectively treating cancers within bone. John Wiley and Sons Inc. 2019-10-22 2019-12 /pmc/articles/PMC6890452/ /pubmed/31553485 http://dx.doi.org/10.1111/cas.14203 Text en © 2019 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
Nakamura, Yu A.
Okuyama, Shuhei
Furusawa, Aki
Nagaya, Tadanobu
Fujimura, Daiki
Okada, Ryuhei
Maruoka, Yasuhiro
Eclarinal, Philip C.
Choyke, Peter L.
Kobayashi, Hisataka
Near‐infrared photoimmunotherapy through bone
title Near‐infrared photoimmunotherapy through bone
title_full Near‐infrared photoimmunotherapy through bone
title_fullStr Near‐infrared photoimmunotherapy through bone
title_full_unstemmed Near‐infrared photoimmunotherapy through bone
title_short Near‐infrared photoimmunotherapy through bone
title_sort near‐infrared photoimmunotherapy through bone
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890452/
https://www.ncbi.nlm.nih.gov/pubmed/31553485
http://dx.doi.org/10.1111/cas.14203
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