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Fluorescent imaging for cancer therapy and cancer gene therapy

The translation of laboratory science into effective clinical cancer therapy is gaining momentum more rapidly than any other time in history. Understanding cancer cell-surface receptors, cancer cell growth, and cancer metabolic pathways has led to many promising molecular-targeted therapies and canc...

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Detalles Bibliográficos
Autores principales: Woo, Yanghee, Chaurasiya, Shyambabu, O’Leary, Michael, Han, Ernest, Fong, Yuman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531657/
https://www.ncbi.nlm.nih.gov/pubmed/34729398
http://dx.doi.org/10.1016/j.omto.2021.06.007
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author Woo, Yanghee
Chaurasiya, Shyambabu
O’Leary, Michael
Han, Ernest
Fong, Yuman
author_facet Woo, Yanghee
Chaurasiya, Shyambabu
O’Leary, Michael
Han, Ernest
Fong, Yuman
author_sort Woo, Yanghee
collection PubMed
description The translation of laboratory science into effective clinical cancer therapy is gaining momentum more rapidly than any other time in history. Understanding cancer cell-surface receptors, cancer cell growth, and cancer metabolic pathways has led to many promising molecular-targeted therapies and cancer gene therapies. These same targets may also be exploited for optical imaging of cancer. Theoretically, any antibody or small molecule targeting cancer can be labeled with bioluminescent or fluorescent agents. In the laboratory setting, fluorescence imaging (FI) and bioluminescence imaging (BLI) have long been used in preclinical research for quantification of tumor bulk, assessment of targeting of tumors by experimental agents, and discrimination between primary and secondary effects of cancer treatments. Many of these laboratory techniques are now moving to clinical trials. Imageable engineered fluorescent probes that are highly specific for cancer are being advanced. This will allow for the identification of tumors for staging, tracking novel therapeutic agents, assisting in adequate surgical resection, and allowing image-guided biopsies. The critical components of FI include (1) a fluorescent protein that is biologically safe, stable, and distinctly visible with a high target to background ratio and (2) highly sensitive optical detectors. This review will summarize the most promising optical imaging agents and detection devices for cancer clinical research and clinical care.
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spelling pubmed-85316572021-11-01 Fluorescent imaging for cancer therapy and cancer gene therapy Woo, Yanghee Chaurasiya, Shyambabu O’Leary, Michael Han, Ernest Fong, Yuman Mol Ther Oncolytics Review The translation of laboratory science into effective clinical cancer therapy is gaining momentum more rapidly than any other time in history. Understanding cancer cell-surface receptors, cancer cell growth, and cancer metabolic pathways has led to many promising molecular-targeted therapies and cancer gene therapies. These same targets may also be exploited for optical imaging of cancer. Theoretically, any antibody or small molecule targeting cancer can be labeled with bioluminescent or fluorescent agents. In the laboratory setting, fluorescence imaging (FI) and bioluminescence imaging (BLI) have long been used in preclinical research for quantification of tumor bulk, assessment of targeting of tumors by experimental agents, and discrimination between primary and secondary effects of cancer treatments. Many of these laboratory techniques are now moving to clinical trials. Imageable engineered fluorescent probes that are highly specific for cancer are being advanced. This will allow for the identification of tumors for staging, tracking novel therapeutic agents, assisting in adequate surgical resection, and allowing image-guided biopsies. The critical components of FI include (1) a fluorescent protein that is biologically safe, stable, and distinctly visible with a high target to background ratio and (2) highly sensitive optical detectors. This review will summarize the most promising optical imaging agents and detection devices for cancer clinical research and clinical care. American Society of Gene & Cell Therapy 2021-06-24 /pmc/articles/PMC8531657/ /pubmed/34729398 http://dx.doi.org/10.1016/j.omto.2021.06.007 Text en © 2021. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Woo, Yanghee
Chaurasiya, Shyambabu
O’Leary, Michael
Han, Ernest
Fong, Yuman
Fluorescent imaging for cancer therapy and cancer gene therapy
title Fluorescent imaging for cancer therapy and cancer gene therapy
title_full Fluorescent imaging for cancer therapy and cancer gene therapy
title_fullStr Fluorescent imaging for cancer therapy and cancer gene therapy
title_full_unstemmed Fluorescent imaging for cancer therapy and cancer gene therapy
title_short Fluorescent imaging for cancer therapy and cancer gene therapy
title_sort fluorescent imaging for cancer therapy and cancer gene therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531657/
https://www.ncbi.nlm.nih.gov/pubmed/34729398
http://dx.doi.org/10.1016/j.omto.2021.06.007
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