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An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model

Malignant gliomas are the most common and aggressive primary brain tumor in adults, and high mitotic rates are associated with their malignancy. Gliomas were modeled in mice using the Sleeping Beauty system to encode genetic lesions recapitulating the human disease. The presented workflow allows the...

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Autores principales: Garcia-Fabiani, Maria B., Kadiyala, Padma, Lowenstein, Pedro R., Castro, Maria G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518519/
https://www.ncbi.nlm.nih.gov/pubmed/32984853
http://dx.doi.org/10.1016/j.xpro.2020.100044
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author Garcia-Fabiani, Maria B.
Kadiyala, Padma
Lowenstein, Pedro R.
Castro, Maria G.
author_facet Garcia-Fabiani, Maria B.
Kadiyala, Padma
Lowenstein, Pedro R.
Castro, Maria G.
author_sort Garcia-Fabiani, Maria B.
collection PubMed
description Malignant gliomas are the most common and aggressive primary brain tumor in adults, and high mitotic rates are associated with their malignancy. Gliomas were modeled in mice using the Sleeping Beauty system to encode genetic lesions recapitulating the human disease. The presented workflow allows the study of the proliferation of glioma cells in vivo, enabling the identification of different phases of the cell cycle, with the advantage that 5-ethynyl-2′-deoxyuridine staining does not involve denaturation steps and samples do not require histological processing. For complete details on the use and execution of this protocol, please refer to Núñez et al. (2019).
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spelling pubmed-75185192020-09-25 An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model Garcia-Fabiani, Maria B. Kadiyala, Padma Lowenstein, Pedro R. Castro, Maria G. STAR Protoc Protocol Malignant gliomas are the most common and aggressive primary brain tumor in adults, and high mitotic rates are associated with their malignancy. Gliomas were modeled in mice using the Sleeping Beauty system to encode genetic lesions recapitulating the human disease. The presented workflow allows the study of the proliferation of glioma cells in vivo, enabling the identification of different phases of the cell cycle, with the advantage that 5-ethynyl-2′-deoxyuridine staining does not involve denaturation steps and samples do not require histological processing. For complete details on the use and execution of this protocol, please refer to Núñez et al. (2019). Elsevier 2020-06-06 /pmc/articles/PMC7518519/ /pubmed/32984853 http://dx.doi.org/10.1016/j.xpro.2020.100044 Text en © 2020 The Author(s) http://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 Protocol
Garcia-Fabiani, Maria B.
Kadiyala, Padma
Lowenstein, Pedro R.
Castro, Maria G.
An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model
title An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model
title_full An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model
title_fullStr An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model
title_full_unstemmed An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model
title_short An Optimized Protocol for In Vivo Analysis of Tumor Cell Division in a Sleeping Beauty-Mediated Mouse Glioma Model
title_sort optimized protocol for in vivo analysis of tumor cell division in a sleeping beauty-mediated mouse glioma model
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518519/
https://www.ncbi.nlm.nih.gov/pubmed/32984853
http://dx.doi.org/10.1016/j.xpro.2020.100044
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