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Application of GFP imaging in cancer

Multicolored proteins have allowed the color coding of cancer cells growing in vivo and enabled the distinction of host from tumor with single-cell resolution. Non-invasive imaging with fluorescent proteins enabled follow the dynamics of metastatic cancer to be followed in real time in individual an...

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Autor principal: Hoffman, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383682/
https://www.ncbi.nlm.nih.gov/pubmed/25686095
http://dx.doi.org/10.1038/labinvest.2014.154
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author Hoffman, Robert M.
author_facet Hoffman, Robert M.
author_sort Hoffman, Robert M.
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description Multicolored proteins have allowed the color coding of cancer cells growing in vivo and enabled the distinction of host from tumor with single-cell resolution. Non-invasive imaging with fluorescent proteins enabled follow the dynamics of metastatic cancer to be followed in real time in individual animals. Non-invasive imaging of cancer cells expressing fluorescent proteins has enabled the real-time determination of efficacy of candidate antitumor and antimetastatic agents in mouse models. The use of fluorescent proteins to differentially label cancer cells in the nucleus and cytoplasm allow visualization of the nuclear–cytoplasmic dynamics of cancer cells in vivo, mitosis, apoptosis, cell-cycle position and differential behavior of nucleus and cytoplasm such as occurs during cancer-cell deformation and extravasation. Recent applications of the technology described here include linking fluorescent proteins with cell-cycle-specific proteins (FUCCI) such that the cells change color from red to green as they transit from G1 to S phases. With the macro and micro imaging technologies described here, essentially any in vivo process can be imaged, enabling the new field of in vivo cell biology using fluorescent proteins.
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spelling pubmed-43836822015-10-01 Application of GFP imaging in cancer Hoffman, Robert M. Lab Invest Article Multicolored proteins have allowed the color coding of cancer cells growing in vivo and enabled the distinction of host from tumor with single-cell resolution. Non-invasive imaging with fluorescent proteins enabled follow the dynamics of metastatic cancer to be followed in real time in individual animals. Non-invasive imaging of cancer cells expressing fluorescent proteins has enabled the real-time determination of efficacy of candidate antitumor and antimetastatic agents in mouse models. The use of fluorescent proteins to differentially label cancer cells in the nucleus and cytoplasm allow visualization of the nuclear–cytoplasmic dynamics of cancer cells in vivo, mitosis, apoptosis, cell-cycle position and differential behavior of nucleus and cytoplasm such as occurs during cancer-cell deformation and extravasation. Recent applications of the technology described here include linking fluorescent proteins with cell-cycle-specific proteins (FUCCI) such that the cells change color from red to green as they transit from G1 to S phases. With the macro and micro imaging technologies described here, essentially any in vivo process can be imaged, enabling the new field of in vivo cell biology using fluorescent proteins. 2015-02-16 2015-04 /pmc/articles/PMC4383682/ /pubmed/25686095 http://dx.doi.org/10.1038/labinvest.2014.154 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Hoffman, Robert M.
Application of GFP imaging in cancer
title Application of GFP imaging in cancer
title_full Application of GFP imaging in cancer
title_fullStr Application of GFP imaging in cancer
title_full_unstemmed Application of GFP imaging in cancer
title_short Application of GFP imaging in cancer
title_sort application of gfp imaging in cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383682/
https://www.ncbi.nlm.nih.gov/pubmed/25686095
http://dx.doi.org/10.1038/labinvest.2014.154
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