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Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors

[Image: see text] Surgery is the preferred treatment option for most solid tumors. However, inaccurate detection of cancer borders leads to either incomplete removal of malignant cells or excess excision of healthy tissue. While fluorescent contrast agents and imaging systems improve tumor visualiza...

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Autores principales: Faucher, Franco F., Liu, Kevin J., Cosco, Emily D., Widen, John C., Sorger, Jonathan, Guerra, Matteo, Bogyo, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214504/
https://www.ncbi.nlm.nih.gov/pubmed/37252358
http://dx.doi.org/10.1021/acscentsci.3c00261
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author Faucher, Franco F.
Liu, Kevin J.
Cosco, Emily D.
Widen, John C.
Sorger, Jonathan
Guerra, Matteo
Bogyo, Matthew
author_facet Faucher, Franco F.
Liu, Kevin J.
Cosco, Emily D.
Widen, John C.
Sorger, Jonathan
Guerra, Matteo
Bogyo, Matthew
author_sort Faucher, Franco F.
collection PubMed
description [Image: see text] Surgery is the preferred treatment option for most solid tumors. However, inaccurate detection of cancer borders leads to either incomplete removal of malignant cells or excess excision of healthy tissue. While fluorescent contrast agents and imaging systems improve tumor visualization, they can suffer from low signal-to-background and are prone to technical artifacts. Ratiometric imaging has the potential to eliminate many of these issues such as uneven probe distribution, tissue autofluorescence, and changes in positioning of the light source. Here, we describe a strategy to convert quenched fluorescent probes into ratiometric contrast agents. Conversion of the cathepsin-activated probe, 6QC-Cy5, into a two-fluorophore probe, 6QC-RATIO, significantly improved signal-to-background in vitro and in a mouse subcutaneous breast tumor model. Tumor detection sensitivity was further enhanced using a dual-substrate AND-gate ratiometric probe, Death-Cat-RATIO, that fluoresces only after orthogonal processing by multiple tumor-specific proteases. We also designed and built a modular camera system that was coupled to the FDA-approved da Vinci Xi robot, to enable real-time imaging of ratiometric signals at video frame rates compatible with surgical workflows. Our results demonstrate that ratiometric camera systems and imaging probes have the potential to be clinically implemented to improve surgical resection of many types of cancer.
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spelling pubmed-102145042023-05-27 Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors Faucher, Franco F. Liu, Kevin J. Cosco, Emily D. Widen, John C. Sorger, Jonathan Guerra, Matteo Bogyo, Matthew ACS Cent Sci [Image: see text] Surgery is the preferred treatment option for most solid tumors. However, inaccurate detection of cancer borders leads to either incomplete removal of malignant cells or excess excision of healthy tissue. While fluorescent contrast agents and imaging systems improve tumor visualization, they can suffer from low signal-to-background and are prone to technical artifacts. Ratiometric imaging has the potential to eliminate many of these issues such as uneven probe distribution, tissue autofluorescence, and changes in positioning of the light source. Here, we describe a strategy to convert quenched fluorescent probes into ratiometric contrast agents. Conversion of the cathepsin-activated probe, 6QC-Cy5, into a two-fluorophore probe, 6QC-RATIO, significantly improved signal-to-background in vitro and in a mouse subcutaneous breast tumor model. Tumor detection sensitivity was further enhanced using a dual-substrate AND-gate ratiometric probe, Death-Cat-RATIO, that fluoresces only after orthogonal processing by multiple tumor-specific proteases. We also designed and built a modular camera system that was coupled to the FDA-approved da Vinci Xi robot, to enable real-time imaging of ratiometric signals at video frame rates compatible with surgical workflows. Our results demonstrate that ratiometric camera systems and imaging probes have the potential to be clinically implemented to improve surgical resection of many types of cancer. American Chemical Society 2023-05-04 /pmc/articles/PMC10214504/ /pubmed/37252358 http://dx.doi.org/10.1021/acscentsci.3c00261 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Faucher, Franco F.
Liu, Kevin J.
Cosco, Emily D.
Widen, John C.
Sorger, Jonathan
Guerra, Matteo
Bogyo, Matthew
Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors
title Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors
title_full Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors
title_fullStr Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors
title_full_unstemmed Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors
title_short Protease Activated Probes for Real-Time Ratiometric Imaging of Solid Tumors
title_sort protease activated probes for real-time ratiometric imaging of solid tumors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214504/
https://www.ncbi.nlm.nih.gov/pubmed/37252358
http://dx.doi.org/10.1021/acscentsci.3c00261
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