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The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma
PURPOSE: Conjunctival squamous cell carcinoma (SCC) is a sight-threatening ocular surface malignancy with the primary treatment modality being surgical resection. To evaluate surgical imaging modalities to improve surgical resection, we established a novel murine model for conjunctival SCC to demons...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344218/ https://www.ncbi.nlm.nih.gov/pubmed/35895055 http://dx.doi.org/10.1167/tvst.11.7.23 |
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author | Youn, Gun Min Case, Ayden G. Jarin, Trent Li, BaoXiang Swarup, Aditi Naranjo, Andrea Bou-Khalil, Charbel Yao, Jacqueline Zhou, Quan Hom, Marisa E. Rosenthal, Eben L. Wu, Albert Y. |
author_facet | Youn, Gun Min Case, Ayden G. Jarin, Trent Li, BaoXiang Swarup, Aditi Naranjo, Andrea Bou-Khalil, Charbel Yao, Jacqueline Zhou, Quan Hom, Marisa E. Rosenthal, Eben L. Wu, Albert Y. |
author_sort | Youn, Gun Min |
collection | PubMed |
description | PURPOSE: Conjunctival squamous cell carcinoma (SCC) is a sight-threatening ocular surface malignancy with the primary treatment modality being surgical resection. To evaluate surgical imaging modalities to improve surgical resection, we established a novel murine model for conjunctival SCC to demonstrate the utility of panitumumab-IRDye800, a fluorescently labeled anti-epidermal growth factor receptor (EGFR) antibody. METHODS: NOD-scid IL2Rgamma(null) (NSG) mice received subconjunctival injection of UM-SCC-1 or SCC-9, head and neck SCC cell lines. On tumor growth, mice were injected with Panitumumab-IRDye800CW, and imaged with a small animal imaging system and optical coherence tomography (OCT). Immunohistochemistry for SCC markers were used to confirm tumor origin. RESULTS: Seventy-five percent (N = 4) of the UM-SCC-1 group developed aggressive, rapidly growing tumors that were P40 and EGFR positive within two weeks of inoculation. The SCC-9 tumors failed to demonstrate any growth (N = 4). Ocular tumors demonstrated high fluorescence levels with a tumor to background ratio of 3.8. CONCLUSIONS: Subconjunctival injections are an appropriate technique to create in vivo models for assessing treatment modalities and novel therapies in conjunctival SCC. TRANSLATIONAL RELEVANCE: This model demonstrates Panitumumab-IRDye800CW's utility in the ophthalmic setting and suggests that clinical trials may be warranted. |
format | Online Article Text |
id | pubmed-9344218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-93442182022-08-03 The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma Youn, Gun Min Case, Ayden G. Jarin, Trent Li, BaoXiang Swarup, Aditi Naranjo, Andrea Bou-Khalil, Charbel Yao, Jacqueline Zhou, Quan Hom, Marisa E. Rosenthal, Eben L. Wu, Albert Y. Transl Vis Sci Technol Ocular Oncology PURPOSE: Conjunctival squamous cell carcinoma (SCC) is a sight-threatening ocular surface malignancy with the primary treatment modality being surgical resection. To evaluate surgical imaging modalities to improve surgical resection, we established a novel murine model for conjunctival SCC to demonstrate the utility of panitumumab-IRDye800, a fluorescently labeled anti-epidermal growth factor receptor (EGFR) antibody. METHODS: NOD-scid IL2Rgamma(null) (NSG) mice received subconjunctival injection of UM-SCC-1 or SCC-9, head and neck SCC cell lines. On tumor growth, mice were injected with Panitumumab-IRDye800CW, and imaged with a small animal imaging system and optical coherence tomography (OCT). Immunohistochemistry for SCC markers were used to confirm tumor origin. RESULTS: Seventy-five percent (N = 4) of the UM-SCC-1 group developed aggressive, rapidly growing tumors that were P40 and EGFR positive within two weeks of inoculation. The SCC-9 tumors failed to demonstrate any growth (N = 4). Ocular tumors demonstrated high fluorescence levels with a tumor to background ratio of 3.8. CONCLUSIONS: Subconjunctival injections are an appropriate technique to create in vivo models for assessing treatment modalities and novel therapies in conjunctival SCC. TRANSLATIONAL RELEVANCE: This model demonstrates Panitumumab-IRDye800CW's utility in the ophthalmic setting and suggests that clinical trials may be warranted. The Association for Research in Vision and Ophthalmology 2022-07-27 /pmc/articles/PMC9344218/ /pubmed/35895055 http://dx.doi.org/10.1167/tvst.11.7.23 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Ocular Oncology Youn, Gun Min Case, Ayden G. Jarin, Trent Li, BaoXiang Swarup, Aditi Naranjo, Andrea Bou-Khalil, Charbel Yao, Jacqueline Zhou, Quan Hom, Marisa E. Rosenthal, Eben L. Wu, Albert Y. The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma |
title | The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma |
title_full | The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma |
title_fullStr | The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma |
title_full_unstemmed | The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma |
title_short | The Use of Panitumumab-IRDye800CW in a Novel Murine Model for Conjunctival Squamous Cell Carcinoma |
title_sort | use of panitumumab-irdye800cw in a novel murine model for conjunctival squamous cell carcinoma |
topic | Ocular Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344218/ https://www.ncbi.nlm.nih.gov/pubmed/35895055 http://dx.doi.org/10.1167/tvst.11.7.23 |
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