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Luciferase fragment complementation imaging in preclinical cancer studies

The luciferase fragment complementation assay (LFCA) enables molecular events to be non-invasively imaged in live cells in vitro and in vivo in a comparatively cheap and safe manner. It is a development of previous enzyme complementation assays in which reporter genes are split into two, individuall...

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Autores principales: Lake, Madryn C., Aboagye, Eric O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278313/
https://www.ncbi.nlm.nih.gov/pubmed/25594026
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author Lake, Madryn C.
Aboagye, Eric O.
author_facet Lake, Madryn C.
Aboagye, Eric O.
author_sort Lake, Madryn C.
collection PubMed
description The luciferase fragment complementation assay (LFCA) enables molecular events to be non-invasively imaged in live cells in vitro and in vivo in a comparatively cheap and safe manner. It is a development of previous enzyme complementation assays in which reporter genes are split into two, individually enzymatically inactive, fragments that are able to complement one another upon interaction. This complementation can be used to externally visualize cellular activities. In recent years, the number of studies which have used LFCAs to probe questions relevant to cancer have increased, and this review summarizes the most significant and interesting of these. In particular, it focuses on work conducted on the epidermal growth factor, nuclear and chemokine receptor families, and intracellular signaling pathways, including IP(3), cAMP, Akt, cMyc, NRF2 and Rho GTPases. LFCAs which have been developed to image DNA methylation and detect RNA transcripts are also discussed.
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spelling pubmed-42783132015-01-15 Luciferase fragment complementation imaging in preclinical cancer studies Lake, Madryn C. Aboagye, Eric O. Oncoscience Review The luciferase fragment complementation assay (LFCA) enables molecular events to be non-invasively imaged in live cells in vitro and in vivo in a comparatively cheap and safe manner. It is a development of previous enzyme complementation assays in which reporter genes are split into two, individually enzymatically inactive, fragments that are able to complement one another upon interaction. This complementation can be used to externally visualize cellular activities. In recent years, the number of studies which have used LFCAs to probe questions relevant to cancer have increased, and this review summarizes the most significant and interesting of these. In particular, it focuses on work conducted on the epidermal growth factor, nuclear and chemokine receptor families, and intracellular signaling pathways, including IP(3), cAMP, Akt, cMyc, NRF2 and Rho GTPases. LFCAs which have been developed to image DNA methylation and detect RNA transcripts are also discussed. Impact Journals LLC 2014-06-01 /pmc/articles/PMC4278313/ /pubmed/25594026 Text en © 2014 Lake and Aboagye http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Lake, Madryn C.
Aboagye, Eric O.
Luciferase fragment complementation imaging in preclinical cancer studies
title Luciferase fragment complementation imaging in preclinical cancer studies
title_full Luciferase fragment complementation imaging in preclinical cancer studies
title_fullStr Luciferase fragment complementation imaging in preclinical cancer studies
title_full_unstemmed Luciferase fragment complementation imaging in preclinical cancer studies
title_short Luciferase fragment complementation imaging in preclinical cancer studies
title_sort luciferase fragment complementation imaging in preclinical cancer studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278313/
https://www.ncbi.nlm.nih.gov/pubmed/25594026
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